What Scientific Advancement Jobs are in Canada?

**Evidence Disclosure Lead/Scientific Publication Lead**
**About Astellas**
Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com.
**Are you driven to make a real difference in the lives of patients?**
We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.
**Purpose and Scope**
The Evidence Disclosure Lead I leads delivery of evidence disclosures of Astellas-sponsored research, including congress abstracts/ presentations (orals and posters), manuscripts and publication extenders to meet Healthcare Professionals (HCPs) needs and preferences.
This role is responsible for driving effective scientific messaging and storytelling in the evidence disclosures, to provide HCPs with credible data to improve clinical practice for patients.
The Evidence Disclosure Lead I will be part of the Evidence Disclosure Chapter and will be a core member of a brand-specific
Evidence Dissemination Value Team which plans and executes on the integrated evidence dissemination plan for a specific brand in alignment with the Brand Strategy following agile ways of working.
**Essential Job Duties**
**Strategic Planning & Prioritization:**
+ As core member of Evidence Dissemination Value team contributes on applicable portion of the integrated Evidence Dissemination Plan for applicable product following Agile principles for ways of working
+ Collaborates and aligns on integrated Evidence Dissemination Plan with relevant internal stakeholders (e.g. MA Local Brand Team Leads of co-creation countries and Global Medical Leads).
+ Engages with internal stakeholders to understand content and formats needs and feedback on existing content
+ Actively keeps up with industry innovation and evolution of HCPs/ customer content and channel needs and preferences
+ Oversees project progression and timelines in collaboration with internal Scientific Content Creators or external vendors (i.e. budget and vendor management)
**Evidence Disclosure Content Ownership:**
+ Supports authors with scientific narrative, scientific messaging and storytelling for applicable brand
+ Drives and owns creation and delivery of clear, balanced, and evidence-based evidence disclosures by authors. This will include congress abstracts/ presentations (orals and posters), manuscripts and publication extenders.
**Scientific Content Governance:**
+ Accountable for review/approval process in compliance with Astellas SOPs for content owned by this role
+ Reviews and is responsible for ensuring applicable content is aligned with author direction, scientifically accurate, high quality, and fair & balanced in compliance with Astellas processes and procedures and external publication guidance (i.e. GPP, ICMJE, etc).
+ Oversees the addressing of comments/ feedback by authors/reviewers as performed by Scientific Content Creators and resolve escalated complex or conflicting feedback
+ Ensures accurate and timely compliance documentation in publication management system
**Outcome/ impact measurements:**
+ Support collecting and assessment of evidence dissemination outcome/impact metrics and contribute to evidence dissemination value narrative for the applicable brand
+ Assess Evidence Disclosure metrics and optimize accordingly
**Required Qualifications**
+ MSc in a life science or healthcare-related field, with preference for PharmD, Pharmacist, PhD or MD
+ 4+ years' experience Medical Affairs/ Medical Communication role (content creation/delivery and material review)
+ Excellent English written and verbal communication skills
+ Ability to quickly adapt to digital tools and platform
+ Experience in scientific narrative, storytelling and messaging
+ Knowledge on legal/ regulatory/ code requirements for non-promotional content
+ Ability to translate complex scientific knowledge into compelling visuals/ narratives
+ Knowledge of clinical design/ drug development and interpretation of clinical trial results
+ Attention to detail and commitment to quality and compliance
**Preferred:**
+ PhD, PharmD, MD
+ Interest in/ or knowledge of Astellas relevant therapeutic areas
+ Experience and/or knowledge of Agile ways of working
+ Ability to influence without authority and resolve conflicts
+ Ability to manage multiple priorities with successful outcome
+ Experience with AI content generation use
+ Demonstrates Business Acumen
**Location and Working Environment**
+ At Astellas we recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas' Responsible Flexibility Guidelines.
**What awaits you at Astellas?**
+ Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide. Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.
+ Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.
+ A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.
**Our Organizational Values and Behaviors**
**Values:** _Innovation, Integrity_ and _Impact_ sit at the heart of what we do.
**Behaviors:** We come together as _'One Astellas'_ , working with courage and a sense of _urgency_ . We are outcome focused and consistently take _accountability_ for our personal contribution.
**Salary Range:** $108,920 - $155,600 CAD annually per year (final compensation will be determined based on a variety of factors, including but not limited to proficiency levels and organizational equity considerations)
_*The salary range provided applies to Canada only and does not apply to any other locations outside of Canada._
**Benefits:**
+ Medical, Dental and Vision Insurance
+ Generous Paid Time Off options, including Vacation, Sick time and national holidays
+ Registered Retirement Savings Plan Program (RRSP)
+ Company paid life insurance
+ Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
+ Long Term Incentive Plan for eligible positions
+ Wellness programs
Astellas may use artificial intelligence-enabled tools at various stages of the recruitment and selection process.
**Additional information:**
Astellas Pharma Canada welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the hiring process.
_No telephone inquiries, in-person applications, or agencies please. While we appreciate all applications, only candidates under consideration will be contacted._
**\#LI-CH1**
Category Evidence Disclosure
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Scientist I - Development Operations
**Summary:**
Provide analytical support in the Laboratory Operations Department by following standard practices. Assist with method development and evaluation activities. Perform method validations and Research & Development (R&D) analytical testing. Make detailed observations and review, document, and communicate test results.
**Essential Functions:**
+ Document all experimental datain accordance withAttributable, Legible, Contemporaneous,Originaland Accurate (ALCOA).
+ Independently carryout HPLC, dissolution and physicaltesting analysistesting following established procedures Analytical Methods & Standard Operating Procedures (SOPs).
+ Work Proficiency with Empower,NuGenesis,LIMS, SM,MS Word & Excel Software.
+ Perform basic troubleshooting to overcome system suitability failures.
+ Follow method validation protocols and carryout method validation bench work.
+ Support ECS (excipient compatibility study) testing.
+ Recognize and report unexpected or OutOfSpecification (OOS) resultsimmediatelyto the Supervisor and conduct laboratory investigations under direction.
+ Maintain a safe working environment, lab 5Sandreport potential hazards.
+ Perform alternating or rotating shift work (asrequired)
**REQUIRED QUALIFICATIONS**
**Education:**
B.Sc. in chemistry or a related field.
**Experience:**
Previous experience in a science related environment.
**Equivalency** _:_
Equivalent combinations of education, training, and relevant work experience may be considered.
**Knowledge, Skills and Abilities:**
Good understanding of basic chemistry and experience with common laboratory equipment and operation. Good understanding of chromatographic separations. Knowledge of qualitative and quantitative chemical or microbiological analysis. Awareness of quality and regulatory requirements in the pharmaceutical industry. Good problem-solving skills and logical approach to solving scientific problems. Demonstrable interpersonal and communication skills (both oral and written). Ability to read and interpret technical procedures and governmental regulations. Ability to apply mathematical operations to such tasks as determination of test reliability, analysis of variance, and correlation techniques. Works well independently and in a team environment. Demonstrated computer proficiency with Microsoft Office programs. Proficiency in the English Language.
**Standards and Expectations:  **  
Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality systems SOP's and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion.  Actively engage in and adhere to departmental systems in order to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving. Models positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner.  Consistently strives to improve skills and knowledge in related field.    
**Physical Requirements:**
Light physical effort and fatigue. Walks, sits or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.
**Compensation**
The estimated annualized pay range for this position in Ontario is $51,200.00-$65,000.00.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
**Division/Site Specific Information**
Thermo Fisher Scientific offers industry-leading pharma services through our Patheon brand, providing an integrated global network of scientific, technical, regulatory, and quality experts committed to helping deliver medicines to patients faster. The Mississauga site supports all phases of drug product development - from early-phase formulation development to clinical trial material to commercial supply - within the same facility using scalable equipment. The site supports non-GMP and GMP work for highly potent and low-potent compounds, complex formulations, pediatric dosage forms, patent-extension strategies, and conventional oral solid dosage forms.
**Shift Schedule:** During your first 3-4 months you will work day shift 9 AM - 5:30 PM, but our laboratories operate a day and afternoon shift and you may be required to work afternoons which right now is from 2:00 PM- 10:30 PM.
**Discover Impactful Work:**
Provides analytical support in the Laboratory Operations Department by following standard practices. Performs analytical testing as assigned for on prototype, CTM (Clinical Trial Material) and Commercial batches supporting development and/or manufacturing operations. Makes detailed observations and review, document, and communicate test results.
**Day in the Life:**
Documents all experimental data in accordance with Attributable, Legible, Contemporaneous, Original and Accurate (ALCOA).
Independently carries out HPLC, dissolution, GC, and physical testing analysis testing following established procedures Analytical Methods & Standard Operating Procedures (SOPs).
Works Proficiency with Empower, NuGenesis, MS Word & Excel Software.
Performs advanced troubleshooting to overcome system suitability failures.
Prepares data summaries and interprets results.
Recognizes and reports unexpected or Out Of Specification (OOS) results immediately to the Supervisor and conducts laboratory investigations under direction.
Maintain a safe working environment and report potential hazards.
Perform alternating or rotating shift work (as required)
**Keys to Success:**
**Education and Experience:**
Minimum B.Sc. in Chemistry required with 3-4 years experience performing analytical testing as assigned for on prototype to commercial batches supporting development and/or manufacturing operations.
Master's in Chemistry preferred with 2 years experience performing analytical testing as assigned for on prototype to commercial batches supporting development and/or manufacturing operations OR
Minimum 1 year demonstrated proficiency as a Scientist I (internal applicants).
**Equivalency** _:_
Equivalent combinations of education, training, and relevant work experience may be considered.
**Knowledge, Skills and Abilities:**
Good understanding of basic chemistry and experience with common laboratory equipment and operation. Advanced understanding of chromatographic separations. Knowledge of qualitative and quantitative chemical or microbiological analysis. Awareness of quality and regulatory requirements in the pharmaceutical industry. Good problem-solving skills and logical approach to solving scientific problems. Demonstrable interpersonal and communication skills (both oral and written). Ability to read and interpret technical procedures and governmental regulations. Ability to apply mathematical operations to such tasks as determination of test reliability, analysis of variance, and correlation techniques. Works well independently and in a team environment. Demonstrated computer proficiency with Microsoft Office programs. Proficiency in the English Language.
**Physical Requirements:**
Position requires ordinary ambulatory skills and physical coordination sufficient to move about lab/office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.
**Excellent Benefits**
+ Benefits & Total Rewards | Thermo Fisher Scientific ( Medical, Dental, & Vision benefits-effective Day 1
+ Paid Time Off & Designated Paid Holidays
+ Retirement Savings Plan
+ Tuition Reimbursement
**OTHER**
+ Relocation assistance is NOT provided
+ Must be legally authorized to work in Canada
+ Must be able to pass a comprehensive background check
**Compensation**
The estimated annualized pay range for this position in Ontario is $62,000.00-$93,050.00.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**How will you make an impact?**
Next Generation Sequencing (NGS) technology is driving a genomics revolution in clinical routine testing, translational research and reproductive health. As a world leader in NGS technology development, thousands of Ampliseq and Oncomine assays are performed on our Ion Torrent Instruments every day around the globe. You will serve in both a direct sales capacity while also coordinating with the field sales team and work across a highly matrixed sales organization. To be fully effective, the Inside Sales specialist will be trained to have a strong understanding of the NGS workflow.
The NGS Inside Sales Specialist will be responsible for attaining sales quota by prospecting for new accounts, expanding our product portfolio in existing accounts, and maintaining a high level of support for existing customers.
**Location:**
This is an in-person office role, based in Burlington, Ontario.
**Key responsibilities:**
+ Prospects among new and active customers to generate leads and expand commercial funnel.
+ Initiates sales process by scheduling appointments; making initial presentation; understanding customer goals, priorities, and challenges.
+ Coordinates with field teams to progress opportunities through the sales cycle and close sales.
+ Expands sales in existing accounts by introducing new products and services; developing new applications.
+ Documents customer facing activities within our customer relationship management (CRM) system. Support pipeline management and sales tracking with use of CRM system and other designated IT tools.
+ Use Strategic Selling techniques within assigned accounts at all levels of the organization which influence purchasing decisions. Develop, write, and execute a business plan for managing assigned territory annually, updated quarterly.
**Key Competency Requirements:**
+ Excellent presentation, verbal and written communication skills
+ Interpersonal effectiveness and rapport building
+ Self-directed, persistent, and goal-oriented
+ Strong prospecting, discovery, sales, objection handling and closing skills
+ Team player, able to work effectively with others
**Education and Experience:**
+ Minimum education: Bachelor's Degree in Biology, Molecular Biology, Biochemistry, or related field.
+ Preference for individuals with hands-on laboratory research, selling and/or customer facing experience. Molecular biology and/or sequencing research experience a plus.
+ Prior sales experience an asset.
**Travel Requirements:**
+ Able to lawfully travel to the US as needed for required meetings and customer visits (~10%)
**Our team's culture:**
+ Join a small team of junior, talented, and highly motivated sales professionals.
+ Report to a manager who is focused on both individual development as well as overall team success.
+ Our team is comprised of individuals with diverse backgrounds and skillsets you will be complimenting and adding to the existing skill-base
+ As a Thermo Fisher employee you'll be joining our exciting and award winning corporate culture ( .
+ You'll enjoy a competitive salary and have access to the full range of benefits & rewards ( enjoyed by Thermo Fisher Scientific employees.
**Compensation**
The estimated annualized pay range for this position in Ontario is $50,000.00-$60,000.00.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
Supply Chain Manufacturing
**Job Sub** **Function:**
Manufacturing Assembly
**Job Category:**
Business Enablement/Support
**All Job Posting Locations:**
Toronto, Ontario, Canada
**Job Description:**
Janssen Pharmaceuticals, Inc., part of the Johnson & Johnson Family of Companies, is recruiting for a ( **Bilingual English/French) CAR-T Scientific Operations Lead.**
The Cell Therapy Scientific Advisor & Operations Lead is a hybrid Medical Affairs role dedicated to supporting CAR-T and cell therapy in Canada. The role combines strategic scientific advising with operational leadership by providing expert scientific and medical support for the therapeutic area, establishing trusted peer-to-peer relationships with KOLs and external experts, contributing to evidence generation and medical strategy, and supporting balanced scientific communication. The role also serves as the primary operational point of contact for CAR-T treatment centres on matters related to the provision of JJIM CAR-T products, connecting medical, commercial operations, supply chain, treatment site, and cross-functional stakeholders to enable a best-in-class customer and patient experience across the end-to-end CAR-T journey.
**About Innovative Medicine**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at duties and responsibilities:**
· Establish and maintain trusted peer-to-peer relationships with KOLs and external experts to collaborate on scientific projects, share balanced scientific data as needed, and support the development of clinical publications in accordance with company policies, applicable laws, regulations, and ethical standards.
· Provide strategic scientific support to key stakeholders, including Medical Education, Marketing, Access, Communications, Regulatory Affairs, Medical Affairs, and field-based medical teams.
· Contribute to study design, protocol development, interpretation of results, post-hoc analyses, publication planning, and local company-sponsored evidence generation studies within the therapeutic area.
· Lead or support execution of the Medical Sciences head office strategy, local clinical trial initiatives, Medical Sciences strategic planning, and yearly business planning activities in partnership with the Medical Director.
· Identify emerging scientific and development trends likely to impact the business, develop action plans to address scientific gaps, and identify key opinion leaders for new disease areas aligned to the pipeline.
· Lead the development and review of balanced and credible scientific communication materials, including slide presentations for internal and external use, advisory boards, workshops, and post-congress evidence dissemination.
· Develop and deliver scientific training for internal partners and the MSL team, including education on CAR-T, cell therapy, clinical evidence, and relevant therapeutic area updates.
· Review, analyze, and disseminate medical voice of customer insights to derive strategic implications and develop action plans that support delivery of the medical strategy.
· Serve as a rapid deployment medical resource for critical events and special medical projects requiring significant cross-functional integration, and participate in or represent Medical Sciences on special projects as agreed with the Medical Director.
· Serve as the primary point of contact for Canadian CAR-T treatment centres for matters related to the provision of JJIM CAR-T products, acting as the connection between commercial operations and medical matters within the local CAR-T medical team.
· Manage end-to-end site set-up, certification, qualification, and lifecycle maintenance activities to ensure treatment site and staff readiness to successfully manage cell therapy orders.
· Deliver and coordinate upfront and ongoing education and training for treatment centres on systems, protocols, policies, order fulfillment processes, technology utilization, and Health Canada-aligned training materials.
· Support treatment centre onboarding to the order management IT platform, assist with case management, verify completeness of intake information, and ensure appropriate stakeholders receive timely and accurate patient safety information.
· Inform and support order tracking and operations coordination after order placement, including communication of cell journey status, order fulfillment milestones, pickup, transport, delivery, and timelines with internal and external stakeholders.
· Coordinate with site stakeholders, including CAR-T coordinators, apheresis teams, physicians, pharmacists, research coordinators, and vein-to-vein teams, to synchronize the patient and cell journey and support clinically appropriate slot allocation and utilization.
· Assess severity and urgency of unforeseen issues related to ordering, manufacturing, rescheduling, cancellations, returns, and other exceptions; escalate and facilitate timely resolution of customer inquiries in accordance with company policies.
· Act as the key liaison between internal stakeholders, including batch advocate, local release team, CAR-T Medical Director, local medical leadership, Supply Chain, and the healthcare facility in the event of an out-of-spec product.
· Ensure operational performance and compliance with local and regional regulations, SOPs, data protection, advertising rules, pharmacovigilance requirements, labeling, documentation obligations, and audit or inspection readiness.
**Special requirements:**
· Field-based role with domestic travel to Canadian CAR-T treatment centres for business purposes; treatment centres may be located in different provinces and require both air and ground travel.
· Occasional travel to conferences and the Toronto office may be required; overall travel may be approximately 25-50% depending on business needs.
· Ability to work across Canadian time zones and provide after-hours support for treatment sites that may extend up to two hours beyond normal working hours.
· Bilingual French and English is required.
**Other features of the job:**
**Role features**
· Hybrid field-based role requiring collaboration with treatment centres, internal medical stakeholders, commercial operations, supply chain, and cross-functional partners.
· Requires frequent use of order management and internal IT platforms, timely documentation, and sustained attention to operational details across the patient and cell journey.
· Requires ability to manage uncertainty, urgent operational issues, challenging conversations, and timely handover or escalation with internal and external stakeholders.
· Requires strong customer experience orientation and ability to adapt communication style, channel, and cadence to treatment centre preferences.
**Key working relationships:**
**Internal**
Strong collaboration with Medical Affairs, CAR-T Medical Director, Cell Therapy Strategic Lead, Medical Education, Marketing, Access, Communications, Regulatory Affairs, Pharmacovigilance, Quality, Commercial Operations, Supply Chain, local release team, batch advocate, and other internal business partners to execute scientific strategy, evidence generation, clinical trial initiatives, and operational priorities.
**External**
Trusted peer-to-peer relationships with KOLs, external experts, CAR-T treatment centres, and site stakeholders, including CAR-T coordinators, apheresis teams, physicians, pharmacists, research coordinators, and healthcare facility operations teams.
Responsive scientific, educational, medical, and operational support to enable evidence generation, site readiness, order fulfillment, and a positive cell therapy customer experience.
**Job location:**
Field-based role located in Canada, with travel to Canadian CAR-T treatment centres and regular presence in the Toronto office as required.
**Essential knowledge and skills:**
· Terminal Degree in natural sciences is required (MD, PhD, PharmD), with advanced scientific or clinical training in cellular therapy strongly preferred.
· Minimum 3+ years of relevant experience in a customer-facing role, ideally in a hospital, patient care coordination, local study management, pharmaceutical industry, or role working directly with hospitals and multiple internal stakeholders.
· Minimum 2 years of prior Medical Science Liaison (MSL) experience is required, with demonstrated capabilities in scientific communication, external expert engagement, and development of trusted KOL relationships.
· Demonstrated experience contributing to medical strategy, evidence generation, clinical trial initiatives, protocol development, scientific material review, advisory boards, workshops, publications, and cross-functional medical projects.
· Experience with hospital logistics and operations, hospital systems, order management platforms, customer experience, and project management.
· Strong understanding of CAR-T biology, the end-to-end manufacturing process, patient services, supply chain processes, logistics, and order fulfillment requirements.
· Previous clinical experience as a CAR-T coordinator, experience in a transplant department, cell therapy experience, supply chain experience is an asset.
· Fluency in French and English is required; ability to communicate effectively with healthcare facilities and internal stakeholders across Canada.
· Solutions- and detail-oriented mindset with strong planning, organizational, presentation, facilitation, and project management skills.
· Ability to manage multiple priorities, operational ambiguity, urgent escalations, and challenging conversations while maintaining customer focus and compliance.
· Good knowledge of GCP, SOPs, pharmacovigilance, data protection, advertising rules, documentation standards, and audit or inspection of readiness expectations.
· Demonstrated leadership behaviours and ability to work effectively in a matrix environment with medical, commercial, supply chain, quality, regulatory, and treatment site partners.
**Core competencies required for this role:**
· Scientific acumen and strategic mindset
· Proactive stakeholder engagement
· Operational excellence
· Cross functional leadership
· Insight generation
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.
"If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent's consent for the background check."
**Required Skills:**
**Preferred Skills:**
Accountability, Agile Manufacturing, Assembly Operations, Data Savvy, Execution Focus, Good Manufacturing Practices (GMP), Manufacturing Processes, Manufacturing Science and Technology (MSAT), Mechanical Equipments, Organizing, Plant Operations, Predictive Analytics, Predictive Maintenance, Process Oriented, Repair Management, Technologically Savvy
**The anticipated base pay range for this position is :**
$94,000.00 - $162,150.00
Additional Description for Pay Transparency:

At Gilead Sciences Canada Inc. we take pride in being recognized as one of Greater Toronto's Top Employer 2024. Click here ( to find out why Gilead Sciences Canada is a top employer!
Chez Gilead Sciences Canada Inc., nous sommes fiers d'être reconnus comme l'un des meilleurs employeurs du Grand Toronto pour 2024. Cliquez ici pour ( en savoir plus sur les raisons de notre succès.
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
**Medical Scientist- HIV, Quebec**
Gilead Sciences is seeking a knowledgeable and motivated Medical Scientist (MS) capable of working effectively in a multi-disciplinary team environment. The successful candidate will assume a full-time employment role in the capacity of Medical Scientist or Sr. Medical Scientist in the HIV therapeutic area, and will report to the MS Lead, HIV. The role will be field-based, and requires travel up to 70% of the time. The person must reside in the Greater Montreal Area.
**The Role:**
+ Implements defined goals and objectives aligned with the Medical Affairs Plan of Action and other strategic initiatives within the HIV therapeutic area covering treatment and prevention.
+ Anticipates obstacles and difficulties that may arise in the field and resolves them in a collaborative manner.
+ Works collaboratively with Gilead personnel in Sales, Marketing, Market Access, Clinical Research, Global Safety and Global Medical Affairs.
+ The incumbent travels to appointments, meetings and conferences on a frequent and regular basis, occasionally with short notice.
+ Exhibits Gilead's core values: integrity, inclusion, teamwork, accountability, and excellence.
**Key Responsibilities:**
**Medical Education:**
+ Discusses and presents scientific and clinical data related to Gilead products, and key HIV topics to health care providers, HIV Community, and other internal and external stakeholders, as requested.
+ Responds to on- and off-label clinical inquiries regarding marketed or developmental Gilead products.
+ Disseminates scientific information, as requested, including medical education materials, slide decks, publications, etc. to support clinical practice.
+ Communicates insights regarding HCP perceptions of the HIV treatment and prevention landscape, marketed Gilead and competitor products, and emerging pipeline products.
+ Attends and reports back on National and International conferences, as requested. Participates in internal Gilead key abstract identification and critical evaluation of key scientific information presented at the conference.
+ Reviews current and emerging literature and communicates, as requested, with HCPs, and to internal Gilead colleagues.
**KOL Development:**
+ Establishes, develops and maintains strong relationships with opinion leaders, clinical investigators and healthcare professionals at academic and non-academic settings.
+ Identifies and develops regional and national opinion leader advocates for Gilead products through personal contacts and on-site visits.
+ Connects external HCP and other HIV treatment and prevention stakeholders with internal Gilead colleagues to further education and research collaborations.
+ Creates connections between external HCPs and other HIV Treatment and Prevention community stakeholders to foster education, research and patient care.
**Research/Data Generation Support:**
+ Supports Gilead clinical operations through site/investigator identification and liaising regarding recruitment and enrollment challenges.
+ Supports investigator-sponsored and collaborative research through liaising with investigators on alignment with Gilead strategic priorities and data gaps, and presenting potential study ideas to internal review committees.
+ Identifies publication opportunities and facilitates development of publications as requested.
**Critical Competencies** :
+ Advanced health sciences degree (M.D., Pharm. D., PhD are preferred) with ≥5 years of experience in healthcare or pharmaceutical industry preferred.
+ Two to four years of experience in HIV and/or infectious disease therapeutic area preferred, but not required.
+ Advanced interpersonal skills including demonstrated proficiency in building relationships with opinion leaders in health care professions, and with patient advocacy groups, and the ability to network within the health care community.
+ Excellent oral and written communication skills, strong scientific and business acumen.
+ Excellent project management ability and organizational skills, including the management of multiple priorities and resources, and high attention to detail.
+ Excellent judgment and personal initiative are required.
+ Advanced computer knowledge (Word, PowerPoint, Excel, Outlook, Teams, Concur, Zoom) is required.
+ Must have knowledge of and be willing to comply with all regulatory/compliance policies.
+ Ability to travel 70% of the time; domestic and international travel is required, including potential attendance at conferences which may include occasional weekend travel.
+ Bilingual (French and English) candidates required.
**Gilead Core Values:**
+ Integrity (doing what's right)
+ Teamwork (working together)
+ Excellence (being your best)
+ Accountability (taking personal responsibility)
+ Inclusion (encouraging diversity)
**Gilead Leadership Commitment:**
+ I AM BOLD in aspiration and AGILE in execution.
+ I CARE and make time for people.
+ I LISTEN, speak openly and explain the "why."
+ I TRUST others and myself to make sound decisions.
+ I OWN the impact of my words and actions.
We are committed to creating a healthier world for everyone - no matter the challenges ahead of us. Through bold and transformative science, we're driving innovation that has the potential to become the next generation of life-changing medicines. Our ambition is evident in our mission. Because the impossible is not impossible. It's what's next.
**Scientifique médical VIH -** **Quebec**
Gilead Sciences recherche un scientifique médical (MS) compétent et motivé, capable de travailler efficacement dans un environnement d'équipe multidisciplinaire. Le candidat retenu assumera un rôle à temps plein en tant que scientifique médical dans le domaine thérapeutique du VIH et relèvera du responsable MS, VIH. Le rôle sera basé sur le terrain et nécessitera des déplacements jusqu'à 70 % du temps. Les candidats doivent être basés à **Montréal** .
**Le rôle:**
+ Mettre en œuvre les buts et objectifs définis alignés sur le plan d'action des affaires médicales et d'autres initiatives stratégiques dans le domaine thérapeutique du VIH couvrant le traitement et la prévention.
+ Anticiper les obstacles et les difficultés qui peuvent survenir sur le terrain et les résoudre de manière collaborative.
+ Travailler en collaboration avec le personnel de Gilead dans les domaines des ventes, du marketing, de l'accès au marché, de la recherche clinique, de la sécurité Monde et des affaires médicales Monde.
+ Le titulaire du poste se rendra fréquemment et régulièrement à des rendez-vous, des réunions et des conférences, parfois avec un court préavis.
+ Présenter les valeurs fondamentales de Gilead : intégrité, inclusion, travail d'équipe, responsabilité et excellence **.**
**Responsabilités clés:**
**Formation médicale:**
+ Développer et présenter des données scientifiques et cliniques liées aux produits Gilead et aux sujets clés sur le VIH aux prestataires de soins de santé, à la communauté VIH et à d'autres parties prenantes internes et externes, sur demande.
+ Répondre aux demandes cliniques sur et hors indication concernant les produits Gilead commercialisés ou en développement.
+ Diffuser des informations scientifiques, sur demande, y compris du matériel de formation médicale, des diaporamas, des publications, etc. pour soutenir la pratique clinique.
+ Communiquer des informations sur les perceptions des professionnels de la santé concernant le contexte du traitement et de la prévention du VIH, les produits commercialisés par Gilead et ses concurrents, ainsi que les produits émergents en cours de développement.
+ Assister et rendre compte des conférences nationales et internationales, sur demande. Participer à l'identification interne des résumés clés de Gilead et à l'évaluation critique des informations scientifiques clés présentées lors de la conférence.
+ Examiner la littérature actuelle et émergente et communiquer, sur demande, avec les professionnels de santé et les collègues internes de Gilead.
**Développement de KOL:**
+ Établir, développer et entretenir des relations solides avec les leaders d'opinion, les chercheurs cliniques, les professionnels de la santé et la communauté VIH dans les milieux universitaires et non universitaires.
+ Identifier et former des leaders d'opinion régionaux et nationaux défenseurs des produits Gilead par le biais de contacts personnels et de visites sur place.
+ Mettre en relation les professionnels de santé externes et d'autres parties prenantes du traitement et de la prévention du VIH avec des collègues internes de Gilead pour poursuivre les collaborations en matière d'éducation et de recherche.
+ Créer des liens entre les professionnels de santé externes et d'autres acteurs communautaires du traitement et de la prévention du VIH pour favoriser l'éducation, la recherche et les soins aux patients.
**Prise en charge de la recherche/génération de données:**
+ Soutenir les opérations cliniques de Gilead par l'identification des sites/investigateurs et la liaison concernant les défis de recrutement et d'inscription.
+ Soutenir la recherche collaborative et parrainée par les chercheurs en assurant la liaison avec les chercheurs sur l'alignement sur les priorités stratégiques de Gilead et les lacunes en matière de données, et en présentant des idées d'études potentielles aux comités d'examen internes.
+ Identifier les opportunités de publication et faciliter le développement de publications sur demande.
**Compétences critiques:**
+ Diplôme avancé en sciences de la santé (MD, Pharm. D., PhD sont préférés) avec ≥ 5 ans d'expérience dans les soins de santé ou l'industrie pharmaceutique.
+ Deux à quatre années d'expérience dans le domaine thérapeutique du VIH et/ou des maladies infectieuses, de préférence, mais non obligatoire.
+ Compétences interpersonnelles avancées, y compris la capacité démontrée à établir des relations avec les leaders d'opinion des professions de santé et avec les groupes de défense des patients, et la capacité de réseauter au sein de la communauté des soins de santé.
+ Excellentes compétences en communication orale et écrite, fort sens scientifique et commercial.
+ Excellentes capacités de gestion de projet et compétences organisationnelles, y compris la gestion de multiples priorités et ressources, et une grande attention aux détails.
+ Un excellent jugement et une initiative personnelle sont requis.
+ Des connaissances informatiques avancées (Word, PowerPoint, Excel, Outlook, Teams, Concur, Zoom) sont requises.
+ Doit connaître et être prêt à se conformer à toutes les politiques de réglementation/conformité.
+ Capacité à voyager 70 % du temps ; des déplacements nationaux et internationaux sont nécessaires, y compris une éventuelle participation à des conférences qui peuvent inclure des déplacements occasionnels le week-end.
+ Bilingue français et anglais requis.
**Valeurs fondamentales de Gilead :**
+ Intégrité (faire ce qui est juste)
+ Travail d'équipe (travailler ensemble)
+ Excellence (être le meilleur de vous-même)
+ Responsabilité (assumer la responsabilité personnelle)
+ Inclusion (encourager la diversité)
**Engagement de la direction de Gilead :**
+ JE SUIS AUDACIEUX dans l'aspiration et AGILE dans l'exécution.
+ Je me soucie et je prends du temps pour les gens.
+ J'ÉCOUTE, je parle ouvertement et j'explique le « pourquoi ».
+ Je fais confiance aux autres et à moi-même pour prendre des décisions judicieuses.
+ Je suis responsable de l'impact de mes paroles et de mes actions.
Nous nous engageons à créer un monde plus sain pour tous, quels que soient les défis qui nous attendent. Grâce à une science audacieuse et transformatrice, nous favorisons l'innovation qui a le potentiel de devenir la prochaine génération de médicaments qui changeront la vie. Notre ambition est évidente dans notre mission. Parce que l'impossible n'est pas impossible. C'est la suite.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Discover Impactful Work:**
As a Field Applications Scientist, you will provide technical support and training for our Olink proteomics product portfolio. You'll serve as a scientific advisor, helping customers optimize their workflows and maximize the value of their investments while contributing to our mission of making the world healthier, cleaner, and safer.
**Location:**
This is a remote role based in the Toronto area. Please note that relocation assistance is not provided for this position.
**A Day in the Life:**
+ Provide technical support and training for the Olink proteomics product portfolio
+ Collaborate with sales teams and customers to deliver product demonstrations and applications support and training that enables research and innovation
+ Deliver both pre- and post-sales technical expertise across multiple technology platforms
+ Develop new applications and troubleshoot complex technical issues
+ Build and maintain strong relationships with customers and internal stakeholders
+ Partner cross-functionally with sales, marketing, R&D, and product management teams to ensure customer success and drive business growth through technical excellence.
**Keys to Success:**
**Education**
+ Bachelor's degree in Chemistry, Biochemistry, Molecular Biology, or related field with 5+ years of relevant experience; Advanced degree with 3+ years of relevant experience
**Experience, Knowledge, Skills, Abilities**
+ Demonstrated expertise in method development and technical problem-solving
+ Clear written and verbal communication skills with ability to explain complex concepts to diverse audiences
+ Strong presentation and training capabilities for both technical and non-technical audiences
+ Ability to work independently and collaboratively in a results-oriented environment
+ Experience in project management and ability to handle multiple priorities
+ Customer service orientation and interpersonal skills
+ Ability to build and maintain effective relationships with internal teams and external customers
+ Willingness to travel up to 25-50%
**Other:**
+ Must be eligible to work in Canada without restrictions
+ Must be able to pass a comprehensive background check
**Compensation**
The estimated annualized pay range for this position in Ontario is $84,000.00-$130,000.00.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.
We set and achieve bold ambitions in our fight against the world's most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.  As a **Sr Research Associate, Process Development** at Gilead you will assume a full-time employment role in the capacity of Senior Research Associate, Process Development in Gilead Alberta's Manufacturing Science and Technology (MSAT) department.
This individual will assist, primarily from lab-based activities, process chemistry activities for pharmaceutical APIs. These activities will include scale-down model development and qualification, process optimization, robustness studies, formal process characterization and risk assessments, and process validation. In addition, this individual will support process technology transfer activities, due diligence, and facility fit assessment for internal and external manufacturing facilities.
**Essential Duties and Job Functions:**
+ Plan and safely execute assigned experiments, with increasing independence, which support Manufacturing Science and Technology (MSAT) department activities and project goals.
+ Make key observations during reaction, work-up and isolation.
+ Interpret data effectively, draw conclusions, summarize results and communicate to project and leadership teams.
+ Demonstrate an ability to recognize anomalous or inconsistent results.
+ Recommend alternatives, research new methods and techniques, and proactively seek out senior personnel to discuss potential solutions to problems.
+ Provide regular updates (written and verbal) to the project team supervision.
+ Use strong verbal communication and interpersonal skills to provide insight into the processes used to achieve experimental results.
+ Work with collaborative communication and problem-solving spirit.
**Knowledge, Experience and Skills:**
+ Excellent verbal and written communication skills and strong interpersonal collaboration skills.
+ Strong desire to work in multi-disciplinary teams, learn new skills and proactively solve problems.
+ Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
+ Familiarity with modern purification and analytical techniques, including HPLC, NMR, mass spec.
+ Well-versed in job related software (e.g. Chemdraw, Microsoft Word/Excel/PowerPoint) and scientific literature searching tools (SciFinder, Reaxys,etc.).
+ Familiarity with statistical analysis to evaluate correlations, shifts and trends of chemical processes, and experience of Design of Experiments (DOE) is an asset.
+ Experience with kinetic studies or process analytical technologies (PAT) is an asset.
+ Experience with continuous manufacturing is an asset.
+ Previous experience in manufacturing under GMP is an asset.
**Minimum Qualifications** :
+ MSc in Organic Chemistry (or related discipline) and 0+ years of experience **OR**
+ BSc in Chemistry and 2+ years of experience (Organic Chemistry focused)
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

Description
Success in any organization begins with its people and having a comprehensive understanding of our workforce and how we best utilize their unique skills and experience is paramount to our future success. WISE (Workforce Intelligence powered by Scientific Engineering) delivers the scientific and engineering foundation that powers Amazon's enterprise-wide workforce planning ecosystem. Addressing the critical need for precise workforce planning, WISE enables a closed-loop mechanism essential for ensuring Amazon has the right workforce composition, organizational structure, and geographical footprint to support long-term business needs with a sustainable cost structure.
We are looking for a Applied Scientist to join our ML/AI team to work on Advanced Optimization and LLM solutions. You will partner with Software Engineers, Data Engineers and other Scientists, TPMs, Product Managers and Senior Management to help create world-class solutions. We're looking for people who are passionate about innovating on behalf of customers, demonstrate a high degree of product ownership, and want to have fun while they make history. You will leverage your knowledge in machine learning, advanced analytics, metrics, reporting, and analytic tooling/languages to analyze and translate the data into meaningful insights. You will have end-to-end ownership of operational and technical aspects of the insights you are building for the business, and will play an integral role in strategic decision-making. Further, you will build solutions leveraging advanced analytics that enable stakeholders to manage the business and make effective decisions, partner with internal teams to identify process and system improvement opportunities. As a tech expert, you will be an advocate for compelling user experiences and will demonstrate the value of automation and data-driven planning tools in the People Experience and Technology space.
Key job responsibilities
- Engineering execution - drive crisp and timely execution of milestones, consider and advise on key design and technology trade-offs with engineering teams
- Priority management - manage diverse requests and dependencies from teams
- Process improvements - define, implement and continuously improve delivery and operational efficiency
- Stakeholder management - interface with and influence your stakeholders, balancing business needs vs. technical constraints and driving clarity in ambiguous situations
- Operational Excellence - monitor metrics and program health, anticipate and clear blockers, manage escalations
To be successful on this journey, you love having high standards for yourself and everyone you work with, and always look for opportunities to make our services better.
Internal job description
Basic Qualifications
- 3+ years of building models for business application experience
- PhD, or Master's degree and 4+ years of CS, CE, ML or related field experience
- Experience in patents or publications at top-tier peer-reviewed conferences or journals
- Experience programming in Java, C++, Python or related language
- Experience in any of the following areas: algorithms and data structures, parsing, numerical optimization, data mining, parallel and distributed computing, high-performance computing
Preferred Qualifications
- Experience using Unix/Linux
- Experience in professional software development
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.
The base salary range for this position is listed below. As a total compensation company, Amazon's package may include other elements such as sign-on payments and restricted stock units (RSUs). Final compensation will be determined based on factors including experience, qualifications, and location. Amazon offers comprehensive benefits including health insurance (medical, dental, vision, prescription, basic life & AD&D insurance), Registered Retirement Savings Plan (RRSP), Deferred Profit Sharing Plan (DPSP), paid time off, and other resources to improve health and well-being. We thank all applicants for their interest, however only those interviewed will be advised as to hiring status.
CAN, BC, Vancouver - 149,300.00 - 249,300.00 CAD annually