138 Validation jobs in Canada

Job Description

Salary:

Join us in Advancing the Environmental Global Impact within the Rail Industry

For the past 30 years, ZTR has designed, developed and released products that have a positive environmental impact within the Locomotive Industry. Planning for an environmentally sustainable future means taking action today in preparation for tomorrow. Everyone has a role to play and we take ours seriously.

ZTR offers a casual working environment and a group of friendly and talented industry leaders passionate about combating climate change. We encourage and support employees to find long-term success and explore opportunities that play into their strengths and passions. We value lateral moves as much as vertical promotions; we believe all roles should develop your skills, broaden your experience, and help you continue on a journey to build a rewarding career at ZTR.

What Youll be Doing

Are you passionate about supporting a more sustainable future? Do you enjoy working with talented individuals to solve complex problems? Are you excited to work on truly innovative product development? Are you data-driven and results-oriented? Whether its solving problems, consulting on products with compassion or continuing to train and develop your skills, youll be helping to push an entire industry technologically forward.

As a Sr. Embedded Software Test and Validation within the Product Development group, you are responsible for contributing to complex engineer projects and products and drive technical quality and stability. You will work closely with cross-functional teams, including Product Managers, Designers and other stakeholders to deliver high-quality software and hardware solutions.

Responsibilities

• Design and develop our testing strategy through manual and automation planning
• Collaborate with software developers, project managers, analysts and other quality specialists to develop effective test strategies
• Interpret engineering and business requirements to develop test plans and cases, both manual and automated; and execute test plans as part of product and project releases
• Conduct functional, regression, integration, performance, and system-level testing
• Document detailed test cases, test results and provide actionable feedback to development teams
• Perform root cause analysis of software defects and support debugging efforts
• Demonstrate success and experience testing hardware embedded applications
• Recommend and implement testing tools, processes and environments
• Mentor junior and intermediate testers in best practices

Who Are You?

• 4+ years of experience working in hardware development environment in a quality focused role
• Graduate from a College or University program (Engineering, Software and Information System Testing etc.)
• Strong communication skills, both verbal and written
• Self-motivated to succeed while working in a team-oriented environment
• Experience with requirements gathering tools (ex. Jama, JIRA, Confluence)
• Experience with sensor and off the shelf hardware integration
• Proficient in PLCs (Siemens, Rockwell, etc.)
• Basic understanding of software integration techniques, version control systems and engineering tools (e.g., GitHub, Jira) for efficient collaboration and development practices
• Knowledge of communication protocols such as Profinet, Modbus, CAN, Ethernet etc. is an asset
• Development experience is a plus

Please apply even if you dont qualify for all responsibilities or skills.

Why Choose ZTR?

ZTR is all about our people. That is why we value Diversity, Equity and Inclusion (DEI) within our organization. DEI is essential to our goal of creating a great place to work. We are committed to building a representative workforce and committed to equal opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
We are looking for flexible, compassionate and enthusiastic individuals who thrive in a fast-paced working environment, and who are looking for long-term, meaningful employment in a career that makes a real difference.

At ZTR, we continuously promote a healthy balance between work, fun and family. This is a place where employees make a difference in our company and within our customers organizations. You will have the ability to direct your career path at ZTR as we are rapidly growing with numerous opportunities for professional growth and development.

ZTR Control Systems provides accommodations for applicants with disabilities throughout the recruitment process. If you require accommodation, please contact Human Resources. We will address information received regarding the accommodation needs of applicants in confidence.

Job Description

Salary:

* English Version Follows **

Chez SMARDT, nous ne nous contentons pas de fabriquer des refroidisseurs nous intgrons linnovation, lefficacit et la durabilit dans chaque projet. Nous recherchons un Spcialiste en Conception et Validation qui souhaite voir son travail passer du concept la ralit, en jouant un rle pratique dans la conception, la construction et la validation de systmes de refroidissement haute performance. Si vous tes passionn par la conception mcanique, que vous aimez rsoudre des problmes et que vous vous panouissez dans un environnement collaboratif o vos ides font la diffrence, vous vous sentirez chez vous ici.

Pourquoi vous allez adorer travailler ici :

• Faire partie dun leader mondial de la technologie HVAC durable.
• Voir vos conceptions prendre vie grce aux prototypes et tests en conditions relles.
• Travailler aux cts dune quipe dingnieurs innovants et dexperts du secteur.
• voluer dans une culture qui valorise la crativit, la responsabilit et lamlioration continue.

Vos missions principales :

• Concevoir et dvelopper des composants mcaniques pour les systmes de refroidissement.
• Superviser et coordonner la construction des prototypes, en garantissant la qualit et la conformit.
• Raliser des tests fonctionnels et de validation pour vrifier la performance.
• Diagnostiquer les problmes techniques et proposer des solutions efficaces.
• Fournir un soutien lors de la mise en service, du dmarrage et des tests des systmes.
• Superviser les processus de fabrication et sassurer que lintention de conception est respecte.
• Examiner les plans de production et collaborer avec les quipes transversales.
• Soutenir les projets de R&D et contribuer lamlioration continue des produits.
• Rdiger et maintenir une documentation technique claire et prcise.

Qualifications Profil recherch :

• Ingnieur mcanique avec connaissance des systmes de refroidissement.
• Comptences en conception, tests et diagnostics.
• Exprience en collaboration transversale (R&D la production).
• Diplme de baccalaurat en gnie mcanique.
• 3+ annes dexprience avec les systmes de refroidissement, quipements HVAC ou rfrigration industrielle.
• Matrise des outils CAO 3D (Autodesk Inventor, SolidWorks, etc.) et des principes de conception mcanique.
• Bonne comprhension de la prototypage, des tests de validation et des processus de fabrication.
• Excellentes comptences en rsolution de problmes et souci du dtail.
• Capacit travailler en quipe et communiquer efficacement.

Ce que nous offrons :

• Salaire comptitif et avantages sociaux.
• Opportunit de travailler sur des technologies de pointe dans un environnement collaboratif.
• Opportunits de dveloppement professionnel et dvolution de carrire.
  

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At SMARDT, we dont just build chillers we engineer efficiency, innovation, and sustainability into every project. Were looking for a Design and Validation Specialist who wants to see their work go from concept to reality, playing a hands-on role in designing, building, and validating the next generation of high-performance chiller systems. If youre passionate about mechanical design, love problem-solving, and thrive in a collaborative environment where your ideas make a difference, youll feel right at home here.

Why Youll Love Working Here:

• Be part of a global leader in sustainable HVAC technology.
• See your designs come to life through prototype builds and real-world testing.
• Work alongside a team of innovative engineers and industry experts.
• Enjoy a culture that values creativity, ownership, and continuous improvement.

What Youll Do:

• Design and develop mechanical components for chiller systems.
• Lead and coordinate prototype builds, ensuring quality and compliance.
• Conduct functional and validation testing to verify performance.
• Diagnose technical issues and develop effective solutions.
• Provide commissioning, start-up, and testing support.
• Oversee manufacturing processes and ensure design intent is met.
• Review production drawings and collaborate with cross-functional teams.
• Support R&D projects and contribute to continuous product improvement.
• Prepare clear technical documentation and reports.

Qualifications What Were Looking For:

• Mechanical engineer with chiller systems knowledge.
• Skilled in design, testing, and diagnostics.
• Experienced in cross-functional collaboration (R&D to production).
• Bachelors degree in Mechanical Engineering.
• 3+ years of experience with chiller systems, HVAC equipment, or industrial refrigeration.
• Proficiency in 3D CAD tools (Autodesk Inventor, SolidWorks, etc.) and mechanical design principles.
• Strong understanding of prototyping, validation testing, and manufacturing processes.
• Excellent problem-solving skills and attention to detail.
• Strong communication and teamwork abilities.

What We Offer:

• Competitive salary and benefits package.
• Opportunity to work on cutting-edge technology in a collaborative environment.
• Professional growth and development opportunities.
  

Job Description

LMI Technologies, recognized as one of Canada’s Best Workplaces, is a medium-sized technology company built on a culture of openness, respect and professional excellence. At LMI our staff work passionately toward the common goal of designing and delivering innovative 3D machine vision solutions to OEMs and System Integrators working in industrial factory automation around the world. The result of this teamwork is high-performance, easy-to-implement and cost-effective 3D sensor technologies that deliver the best results in even the most challenging 3D inline inspection applications.

The Automation Validation (AV) Team Lead plays a pivotal role within LMI by providing leadership and oversight of the AV team and the related projects. The Automation and Validation teams projects include new production automation equipment design, product validation, process engineering and overall systems engineering. You will be part of a multidisciplinary team that engages with every department across the organization to ensure our Gocators are designed and manufactured to the highest standard. You will work in a supportive team environment working with exciting technologies.

Working as part of our global Technology (R&D) team, you will report to the Senior Product Engineering Manager and work at our Burnaby head office. You will have oversight of Automation Designer/Engineers in the AV team.

Project duties include: Data analysis, validation test design and analysis, automation equipment design and support, mechanical, electrical, control systems design and process control and design.

• Establishes standards and guidelines for the Automation Validation team which is regularly reviewed and approved by the group manager.
• Make strategic decisions about automation processes based on inputs from multiple departments
• Work with the sensor design team to roll out new product introductions to validate product features and integrate into existing or new automation infrastructure
• Carries out regular design reviews with the team and across departments
• Produce task lists to breakdown project assignments into appropriate level of detail
• Manage delivery expectations against key project milestones 
• Create and oversee standard processes for product validation based on existing ISO and worksafe BC standards
• Employ a scientific & data-driven approach to verify and validate equipment designs; both individually and with the team. 
• Leads Lean-Six-Sigma principles & best practices within the LMI Technology group to assist with product quality improvements and standardization of designs / manufacturing processes 
• Design, Develop, and Optimize micron-level automation equipment for optical manufacturing processes (i.e. alignment and calibration). 
• Identify and implement continuous improvement initiatives
• Produce efficient documentation for knowledge transfer across groups (i.e. design validation, assembly, commissioning, maintenance)
• Ability to interpret technical data to effectively design and support mechatronic systems
• Lead commissioning of new automation equipment or production jigs
• Trains team members and provides input to (or completes) employee performance evaluations
• Maintains day-to-day communication with the team on inter-company teams and functions.

• Degree / Diploma in Mechanical Engineering, Mechatronics, or Electrical/Controls Engineering
• 5-10 years working experience in a related field, with a focus on mechanical design and automation/controls
• Background in leading a team and driving goals and milestones
• Must be able to provide strong leadership and manage engineering staff of like discipline
• Strong fundamentals in data analysis to produce meaningful conclusions
• Strong knowledge of SolidWorks, EPDM and mechanical design principles particularly with respect to CNC-based precision part design
• Familiarity with electrical and wiring diagrams for automation equipment.
• Familiarity with fundamental hand and machine shop tools is valued
• Good working knowledge of motion control systems
• Strong understanding of metrology in application
• Strong understanding of machine vision tools/algorithms is an asset
• Strong understanding of ASME Y14.5 GD&T or ISO GPS Standard
• Background in a role that was focused on lean process and development is an asset.
• Lean and/or Six Sigma Black Belt is an asset
• Must be a “driver” – able to search and track down information as required to support development activities
• Proficiency in communicating concepts and findings with clarity in verbal and written communication
• Experience in design of experiments and the application of scientific methods
• Pursues problem solving with clear understanding of facts and defined test plan and solution strategies
• Strong interpersonal skills are required to function effectively in a team environment across departments
• Strong knowledge of Google G-suite or other Office productivity software
• Knowledge of Python or other coding is an asset
• Experience with presenting project ideas and business cases with accompanying analysis is an asset
• Familiarity with optical systems such as lenses, cameras or filters is an asset

Salary Range: $97,600 - $139,000

If you are interested in this exciting opportunity and working for a fast-growing global technology company with an inspiring and engaging workplace environment, please submit your application to our Human Resources team in confidence by clicking the “Apply Now” button.

While we appreciate your interest in LMI very much, we are only able to respond to candidates selected for further consideration. We look forward to talking to you about the possibilities of beginning a rewarding new chapter of your career!

At LMI Technologies, we are an Equal Opportunity employer and we value the diversity of the people we hire and serve. We strive to build and grow our team that fosters variety in backgrounds, perspectives, experiences and skills. We embrace inclusiveness in our workplace, so we can utilize each person’s talents and strengths.

If you are interested in working for a fast-growing global technology company with an inspiring and engaging workplace environment, we invite you to apply and talk about the possibilities of beginning a rewarding new chapter of your career.

#LMISJ

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Job Description

Salary:

Le Groupe Uni3T est une socit informatique jeune et dynamique qui est active dans les secteurs des sciences de la vie et de l'industrie pharmaceutique. L'entreprise est ne d'une volont de runir et d'unifier sous un mme toit une expertise complte dans le domaine des sciences de la vie. Notre mission est d'amliorer l'accs aux soins et aux produits de sant en fournissant des services de consultation et des solutions technologiques aux entreprises des sciences de la vie.

Notre approche repose sur trois axes principaux. Toutes nos missions commencent par l'obtention d'une vision stratgique hautement aligne avec les besoins de nos clients. Nous travaillons avec nos clients sur la transformation de leurs processus afin de librer le plein potentiel organisationnel. Enfin, notre quipe s'occupe du dploiement des technologies pour optimiser la chane de valeur de l'entreprise grce l'automatisation des processus cls, tout en assurant leur conformit rglementaire aux instances applicables.

Nous sommes la recherche d'un talent pour se joindre notre quipe de services professionnels. Ce professionnel travaillera au sein de notre quipe de spcialistes CSV sur les projets de validations de systmes informatiss (CSV) dans un environnement rglement.

Responsabilits :

Effectuer des vrifications et des examens des documents de commissioning, qualification et validation pour les systmes et les processus de nos clients

Coordonner les projets CSV pour les logiciels et les systmes automatiss

laborer des stratgies et des plans de validation

Coordonner les activits des diffrentes parties prenantes (dpartement informatique, SMEs, utilisateurs finaux, unit qualit, fournisseurs)

Effectuer une analyse des risques et dfinir le processus de qualification

Rdiger et examiner les valuations des risques et les scripts de test applicables conformment aux directives de conformit des GxP (BPF) et du CFR partie 11 et aux procdures de validation

laborer et rviser des livrables du cycle de dveloppement logiciel (SDLC), tels que : plans de validation, requis, spcifications, matrices de traabilit, protocoles de test (IQ, OQ et PQ), rapports de qualification.

Excuter et rviser des protocoles de qualification pour assurer la conformit et le respect des lignes directrices applicables

Participer la rsolution des dviations aux protocoles et procdures

Examiner et modifier les procdures d'opration normalises (SOPs)

Communiquer les approches et les exigences du CSV pendant les runions et les ateliers

Dvelopper et effectuer les formations clients

Qualifications et comptences requises :

Matrise du franais et de l'anglais crits et parls

Solides comptences en communication et en relations interpersonnelles

Intress contribuer l'entreprise tout en apprenant

Proactif et organis

Soucieux du dtail

Fait preuve d'initiative

Minimum de 2 ans d'exprience de travail dans les sciences de la vie ou l'industrie pharmaceutique

Baccalaurat en informatique (scurit, infrastructure, logiciel), gnie (chimie, biomdical, biotechnologie, etc.) ou sciences de la vie (biochimie, chimie, pharmacie, etc.)

Avantages :

Salaire de base comptitif + bonus (bas sur la performance de l'entreprise, de l'quipe et des efforts individuels)

Couverture d'assurance complte par RBC

Cotisations REER

Poste permanent temps plein

Remboursement du forfait tlphone mobile

Culture d'entreprise dynamique avec des opportunits de dveloppement de carrire

Politique de travail hybride (selon les besoins de l'quipe et des clients)
venements d'entreprise rguliers.

Exigences :

Doit tre lgalement admissible travailler au Canada l'endroit indiqu ci-dessus et, le cas chant, doit avoir un permis de travail valide ou un permis d'tudes qui permet au candidat de remplir les exigences du rle.

Peut tre amen se dplacer dans la grande rgion de Montral jusqu'aux bureaux des clients.

Le Groupe Uni3T est un employeur qui souscrit au principe de l'galit d'accs l'emploi. Tous les candidats seront pris en considration pour un emploi sans gard l'ge, la couleur, le cong familial ou pour soins mdicaux, l'identit ou l'expression sexuelle, l'tat matrimonial, la condition mdicale, l'origine nationale, le handicap physique ou mental, l'affiliation politique, la race, la religion, le sexe, l'orientation sexuelle ou toute autre caractristique protge par les lois, rglements et ordonnances applicables.

Nous remercions tous les candidats de leur intrt, mais seuls les candidats slectionns seront contacts.

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Uni3T Group is a young and dynamic IT company active in the life sciences and pharmaceutical industries. The company was born out of a desire to bring together and unify under one roof a complete expertise in the field of life sciences. Our mission is to improve access to health care and products by providing consulting services and technology solutions to life science companies.

Our approach is based on three main axes. Our missions begin with obtaining a strategic vision aligned with the needs of our customers. We work with our clients on transforming their processes to unlock the full organizational potential. Finally, our team takes care of the deployment of technologies to optimize the company's value chain through the automation of key processes, while enforcing regulatory compliance to all applicable regulations.

We are looking for a talent to join our professional services team. This professional will work with our team of CSV specialists on computerized systems validation (CSV) projects in a regulated environment.

Responsibilities:

Perform commissioning, qualification and validation documents checks and reviews for our clients' systems and processes

Coordinate CSV projects for software and automated systems

Development of validation strategies and plans

Coordinate the activities of the various stakeholders (IT department, SMEs, end users, quality unit, suppliers)

Perform a risk analysis and define the qualification process

Write and review applicable risk assessments and test scripts in accordance with GxP (BPF) and CFR Part 11 compliance guidelines and validation procedures

Develop and review deliverables of the software development cycle (SDLC), such as: validation plans, requirements, specifications, traceability matrices, test protocols (IQ, OQ and PQ), qualification reports.

Execute and review qualification protocols to ensure compliance and adherence to applicable guidelines

Participate in protocol and procedure discrepancy resolution

Review and modify standard operating procedures (SOPs)

Communicate CSV approaches and requirements during meetings and workshops

Develop and carry out customer training

Qualifications and skills required:

Fluency in written and spoken French and English

Strong communication and interpersonal skills

Interested in contributing to the business while learning

Proactive and organized

Attention to detail

Demonstrates initiative

Minimum of 2 years of work experience in the life sciences or pharmaceutical industry

Bachelor's degree in computer science (security, infrastructure, software), engineering (chemistry, biomedical, biotechnology, etc.) or life sciences (biochemistry, chemistry, pharmacy, etc.)

Benefits :

Competitive base salary + bonus (based on company and team performance and individual effort)

Comprehensive insurance coverage by RBC

RRSP contributions

Permanent full-time position

Refund of the mobile plan

Dynamic corporate culture with career development opportunities

Work from home hybrid policy (based on team and client needs)
Regular corporate events.

Requirements:

Must be legally eligible to work in Canada at the location indicated above and, if applicable, must have a valid work permit or study permit that allows the candidate to fulfill the requirements of the role.

May be required to travel in the greater Montreal area to client offices.

Uni3T Group is an employer who subscribes to the principle of equal access to employment. All applicants will be considered for employment regardless of age, color, family leave or for medical care, gender identity or expression, marital status, medical condition, origin national, physical or mental disability, political affiliation, race, religion, sex, sexual orientation or any other characteristic protected by applicable laws, regulations and ordinances.

We thank all applicants their interest, but only selected applicants will be contacted.

1. JOB OBJECTIVES

Under the supervision of the Head of Microbiology, the incumbent is responsible for drafting protocols, reports and methods related to the validation, transfer and development of microbiology analytical methods or any other project requiring a solution for microbiology methods.

2. PRIMARY FUNCTIONS

• Drafting of protocols, reports and methods for microbiological validation and transfer according to USP

and Ph.Eur for various products under development.

• Execution of the various protocols required in the validation of Sterility, Endotoxin, Microlimit and Filter

methods.

• Preparation and planning of documentation, materials and consumables required for the completion of

projects and the implementation of procedures.

• Participation in various meetings related to new product development.

• Contribute to OOS investigations related to current analyses.

• Act as an expert within the scope of his/her duties.

• Perform any other related tasks deemed pertinent to the position.

• Adherence to established schedule.

3. EXPERIENCE REQUIREMENT AND APTITUDES

• Bachelor’s degree in Microbiology, Master's degree in Microbiology an asset.

• 3 to 5 years of experience in applied microbiology in the pharmaceutical field, performing and validating

analytical methods in endotoxin, sterility and microlimit microbiology.

• Sound knowledge and understanding of GMP.

• Knowledge of regulations related to method validation and execution.

• Bilinguisme (French and English) and excellent written and oral communication skills.

• Knowledge of computer tools.

• Autonomy, initiative, resourcefulness and leadership skills.

• Sense of organization and prioritization.

• Ability to analyze, synthesize and apply sound judgment.

• Interpersonal communication and problem-solving skills.

• Team spirit and interpersonal skills.

• Ability to manage priorities and work under pressure with tight deadlines/frequent changes of priority.

1. JOB OBJECTIVES

Under the supervision of the Head of Microbiology, the incumbent is responsible for drafting protocols, reports and methods related to the validation, transfer and development of microbiology analytical methods or any other project requiring a solution for microbiology methods.

2. PRIMARY FUNCTIONS

• Drafting of protocols, reports and methods for microbiological validation and transfer according to USP

and Ph.Eur for various products under development.

• Execution of the various protocols required in the validation of Sterility, Endotoxin, Microlimit and Filter

methods.

• Preparation and planning of documentation, materials and consumables required for the completion of

projects and the implementation of procedures.

• Participation in various meetings related to new product development.

• Contribute to OOS investigations related to current analyses.

• Act as an expert within the scope of his/her duties.

• Perform any other related tasks deemed pertinent to the position.

• Adherence to established schedule.

3. EXPERIENCE REQUIREMENT AND APTITUDES

• Bachelor’s degree in Microbiology, Master's degree in Microbiology an asset.

• 3 to 5 years of experience in applied microbiology in the pharmaceutical field, performing and validating

analytical methods in endotoxin, sterility and microlimit microbiology.

• Sound knowledge and understanding of GMP.

• Knowledge of regulations related to method validation and execution.

• Bilinguisme (French and English) and excellent written and oral communication skills.

• Knowledge of computer tools.

• Autonomy, initiative, resourcefulness and leadership skills.

• Sense of organization and prioritization.

• Ability to analyze, synthesize and apply sound judgment.

• Interpersonal communication and problem-solving skills.

• Team spirit and interpersonal skills.

• Ability to manage priorities and work under pressure with tight deadlines/frequent changes of priority.

1. JOB OBJECTIVES

Under the supervision of the Head of Microbiology, the incumbent is responsible for drafting protocols, reports and methods related to the validation, transfer and development of microbiology analytical methods or any other project requiring a solution for microbiology methods.

2. PRIMARY FUNCTIONS

• Drafting of protocols, reports and methods for microbiological validation and transfer according to USP

and Ph.Eur for various products under development.

• Execution of the various protocols required in the validation of Sterility, Endotoxin, Microlimit and Filter

methods.

• Preparation and planning of documentation, materials and consumables required for the completion of

projects and the implementation of procedures.

• Participation in various meetings related to new product development.

• Contribute to OOS investigations related to current analyses.

• Act as an expert within the scope of his/her duties.

• Perform any other related tasks deemed pertinent to the position.

• Adherence to established schedule.

3. EXPERIENCE REQUIREMENT AND APTITUDES

• Bachelor’s degree in Microbiology, Master's degree in Microbiology an asset.

• 3 to 5 years of experience in applied microbiology in the pharmaceutical field, performing and validating

analytical methods in endotoxin, sterility and microlimit microbiology.

• Sound knowledge and understanding of GMP.

• Knowledge of regulations related to method validation and execution.

• Bilinguisme (French and English) and excellent written and oral communication skills.

• Knowledge of computer tools.

• Autonomy, initiative, resourcefulness and leadership skills.

• Sense of organization and prioritization.

• Ability to analyze, synthesize and apply sound judgment.

• Interpersonal communication and problem-solving skills.

• Team spirit and interpersonal skills.

• Ability to manage priorities and work under pressure with tight deadlines/frequent changes of priority.

1. OBJECTIFS DU POSTE

Sous la supervision du responsable microbiologie, le titulaire de ce poste est responsable de la rédaction des protocoles, rapports et méthodes reliés à la validation, le transfert et le développement des méthodes analytiques en microbiologie ou tout autres projets nécessitant une recherche de solution pour les méthodes en microbiologie.

2. PRINCIPALES FONCTIONS

• Rédaction des protocoles, rapports et méthodes de validation et transfert microbiologiques selon USP et

Ph.Eur pour différents produits en développement.

• Exécution des différents protocoles requis dans la validation des méthodes de Stérilité, Endotoxines,

Microlimites et de filtres.

• Préparation et planification de la documentation, du matériel et consommables requis pour la complétion

des projets et la mise en vigueur des procédures.

• Participation aux diverses réunions liées au développement de nouveaux produits.

• Contribution aux investigations liées aux OOS reliés aux analyses courantes.

• Agir en tant qu’expert dans le cadre de ses fonctions.

• Effectuer toute autre tâche connexe jugée pertinente dans le cadre de son poste.

• Respect de la cédule établie

3. EXIGENCES ET APTITUDES

• Baccalauréat en Microbiologie, Maîtrise en Microbiologie un atout.

• 3 à 5 ans d’expérience en microbiologie appliquée dans le domaine pharmaceutique, dans l’exécution et

la validation des méthodes analytique en microbiologiques d’endotoxine, de stérilité et de microlimites

• Solides connaissances et compréhension des BPF

• Connaissances des règlementations reliées à la validation et l’exécution de méthodes

• Bilinguisme (français et anglais) et excellentes aptitudes de communication écrite et orale.

• Connaissance des outils informatiques.

• Autonomie, initiative, débrouillardise et leadership

• Sens de l’organisation, de la priorisation

• Esprit d’analyse et de synthèse et sens de jugement.

• Aptitudes en communication interpersonnelle et résolution de problèmes.

• Esprit d’équipe et sens du relationnel.
• Capacité à gérer les priorités et à travailler sous pression avec des échéanciers serrés/changements fréquents de priorité.