64 Laboratory Testing jobs in Canada

Job Description

As a team member of the Order Fulfillment and Quality Control department, you will be challenged with inspecting electronic equipment while processing against customer purchase orders.

Responsibilities:

• Inspecting electronic equipment configured for customer systems
• Verifying product meets latest hardware and software standards
• Scanning barcode information in an AS/400 system
• Function as a member of the production team
• Comply with OSHA, SDS standards and Evertz H&S Safety Policies and Procedures
• Any other duties as required.

Requirements:

• High school Diploma, technical education an asset but not required
• Experience working in a manufacturing environment
• Excellent verbal and written communication skills, problem solving ability, time management skills and interpersonal skills.
• Comfortable using a computer, familiar with Microsoft Outlook, Word, Excel
• Positive attitude and able to work in a fast paced environment
• Results oriented
• Self-motivated

What we offer:

• Employer funded benefits program
• Competitive total compensation package
• Work-life balance
• Employee Assistance plan
• Employee Discount Platform
• Career progression
• Casual work environment
• Social events and sports teams

About Us:

Evertz Microsystems (TSX:ET) is a leading global manufacturer of broadcast equipment and solutions that deliver content to television sets, on-demand services, WebTV, IPTV, and mobile devices (like phones and tablets). Evertz has expertise in delivering complete end-to-end broadcast solutions for all aspects of broadcast production including content creation, content distribution and content delivery.

Considered as an innovator by their customers, Evertz delivers cutting edge solutions that are unmatched in the industry in both hardware and software. Evertz delivers products and solutions that can be found in major broadcast facilities on every continent. Evertz’ customer base also includes telcos, satellite, cable TV, and IPTV providers.

With over 1700 employees, that include hardware and software engineers, Evertz is one of the leaders in the broadcast industry. Evertz has a global presence with offices located in: Canada, United States, United Kingdom, Germany, United Arab Emirates, India, Hong Kong, China, Singapore, and Australia. Evertz was named one of Canada’s 50 Best Managed Companies, which recognizes excellence in Canadian-owned and Canadian-managed companies. Canada’s 50 Best Managed Companies identifies Canadian corporate success through companies focused on their core vision, creating stakeholder value and excelling in the global economy.

Evertz makes certain there is an equal employment opportunity for all employees and applicants for employment, including persons with disabilities. In compliance with AODA, Evertz will strive to provide accommodation to persons with disabilities in the recruitment process upon request. If you are selected for an interview and you require accommodation due to a disability during the recruitment process, please notify Human Resources upon scheduling your interview.

Thank you for considering a career with Evertz!

Please note, this email address will only respond to requests regarding privacy concerns. This inbox will not respond to job applications, resumes, or questions regarding an application. When you apply to a job on this site, the personal data contained in your application will be collected by Evertz Microsystems Ltd (“Controller”), which is located at 5292 John Lucas Drive, Burlington, Ontario, Canada and can be contacted by emailing Controller’s data protection officer is Nadiera Toolsieram, who can be contacted at Your personal data will be processed for the purposes of managing Controller’s and its' subsidiaries' and affiliates' recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) 2016/679 (General Data Protection Regulation) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.

A complete privacy policy can be found at

Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment. Under the GDPR, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with an EU supervisory authority.

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Job Description

Job description

A Little bit about us

Treasure Mills is a family-owned Canadian business founded in 2003. We were one of the first companies in North America to make the claim nut and peanut free under our brand School Safe. Our company is known as the most trusted brand in kids snack foods. We believe in producing sustainable food that allows families to reinforce healthy, active diets that build a brighter future. Our 100% recyclable packages are now environmentally sustainable. By passionately striving through research and development, we utilize ethically sourced, natural ingredients in our innovative products for a taste that is simply delicious.

About the Role

• Responsible for execution of production schedule in a timely manner and within all quality parameters to produce safe quality food
• Set and communicate job expectations to hourly employees; planning of training; monitoring; appraising job results; coaching; employee discipline; initiating, coordinating, and enforcing systems, policies, and procedures
• Proactive involvement in maintaining safety rules, conducting safety meetings, employee safety education, and improving safety awareness throughout the organization
• Schedules equipment and personnel to ensure production requirements/targets are met on a timely basis
• Adhere to product specification requirements throughout the manufacturing process to maintain the desired product quality results
• Suggest changes in work flow processes and use of equipment to increase efficiency of the department and/or production staff to maintain the lowest level of downtime and product costs possible
• Generate daily, weekly, and monthly reports to effectively monitor production targets, financial efficiency, on-time delivery, continuous improvement efforts, and manufacturing issues
• Ability to perform setup, operation, cleanup, for each line equipment
• Work with the maintenance department to assist in prevention / rectification of breakdowns
• Work with the Quality department to prevent and resolve quality issues and root cause analysis
• Adhere to plant policies and procedures, including SQF, HACCP (Hazard Analysis Critical Control Points) and GMP (Good Manufacturing Practices)
• Lead operation of the production team to ensure that quantitative and qualitative measures are met, including those related to standard costs; cost reductions; productivity; health and safety; GMP; sanitation; customer satisfaction
• Promote a focus on excellence in all production activities including those required to support optimal quality, yield, and cost containment, and minimal re-work
• Work closely with senior management team to develop and enforce company quality, health & safety, and productivity goals while ensuring all targets are met and maintained.
• Responsible for minimizing scrap and maximizing efficiency and productivity.
• Conduct labour tracking or production orders and demonstrate accountability on productivity of the operators

Requirements

• 3+ years experience in food processing or manufacturing environment, bakery experience preferred
• Minimum of 2 years supervisory experience
• Have knowledge of health and safety standards, SQF, HACCP & GMP
• Degree or Diploma in Industrial, Mechanical, Manufacturing Engineering, Science or related areas of focus
• Strong mechanical aptitude
• Microsoft Office knowledge required
• Exceptional organizational, communication, time-management and leadership skills
• Must be a strong leader and passionate about quality and food safety
• Forklift licence and experience is considered an asset
• Ability to lift/push/pull 30 pounds
• Be able to stand for lengthy periods
• Flexibility with work hours and the ability to work different shifts with overtime and weekends, as needed

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 Quality Manager delegates the Quality Control (QC) Technologist the authority to independently perform quality control activities for new and repaired products at different stages of the assembly process; conduct incoming quality control and outgoing quality control, ensuring conformity of product or component according to engineering specifications, work instructions and quality standard requirements.

The QC Technologist reports directly to the Quality Team Lead and is part of the Quality team at our Burnaby head office. The QC Technologist will work closely with Manufacturing, Manufacturing Engineering, Purchasing and R&D Teams. With direction from the Quality Manager and Team Lead, the QC Technologist performs duties and assignments under the supervision of Quality Engineers. This will be a temporary position of 6 months. 

Typical duties, responsibilities and activities include:

• Perform daily quality control inspection (incoming, in-process and final inspection) based on sampling plans and inspection sheet or as directed by Quality Engineer/Quality Manager.
• Verify supplier documentation and certificates of compliance.
• Record inspection results and escalate discrepancies to the quality team.
• Support material quarantine, labeling, and tracking of nonconforming incoming and in process materials, sub-assemblies or final product, following Non-Conformance (NC) and Material Review Board process.
• Support and monitor of the First Article Approval (FAA) process flow for the production parts approval process (PPAP).
• Assist in generating quality records: Non Conformance Report (NCR), Problem Reports, First Article Inspection (FAI) reports, First Article Approval (FAA) report, Deviation Allowance.
• Responsible for the integrity of all quality control processes and records, including Incoming (IQC), Outgoing (OQC), Return Material Authorizations (RMA), Non-Conformities (NC) and FAA/PPAP logs, ensuring compliance with quality standards and timely resolution of quality-related concerns.
• Support the Quality Specialist in the disposition of non-conforming parts and collaborate with production teams to investigate and resolve manufacturing issues.
• Perform on-time transaction on MRP system (Netsuite) for Non-conforming Parts, First Article approval and Return Material Authorizations.
• Responsible for maintaining inspection tools, equipment or jig calibration as required.
• Verify that production follows work instructions and quality standards, identifying and containing during assembly or test processes.
• Assist in gathering data for quality reports and metrics.
• Participates in Continuous Improvement activities to improve product and process quality.

• Mechanical or Electronics Technology Diploma or equivalent experience in a manufacturing or electronics environment.
• 5 years hands-on inspection with electronics, metal components and assemblies or working experience in assembly or manufacturing.
• Strong experience using measuring devices like microscopes, calipers, micrometers and various basic recording tools is required.
• Ability to read drawings and knowledge of GD&T.
• Familiarity with inspection documentation and quality records.
• Knowledge of electronics assembly, optics or mechanical parts is preferred.
• 1- 2 year experience in IPC-A-610 (Acceptability of Electronics Assembly) is desired.
• Knowledge of J-STD-001 (Requirements for Soldered Electrical and Electronic Assemblies) is preferred.
• Knowledge of IPC 7711/7721 (Rework, Modification and Repair of Electronic Assemblies) is preferred.
• Knowledge of Basic Statistical Tools (Pareto, Histogram, Grant Charts) is preferred.
• Knowledge of Enterprise MRP systems (Oracle, Netsuite, SAP, Epicor) and QMS is required.

• Ability to communicate and read effectively in English is required.
• Strong attention to detail and ability to follow procedures accurately.
• Team-oriented with strong communication skills.
• Organized, proactive, and accountable.
• Problem-solving mindset.
• Willingness to learn and support multiple tasks as needed.
• Ability to work independently or with minimal or no supervision in a multi disciplinary team.

Salary Range: $ 26 - $ 38

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.

We assure you, once you complete your application, your information is safe with us. To learn more about how we use your personal data, please review our Privacy Policy ( -policy).

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Job Description

The Quality Control Technician (QCT) must be detail oriented and have a high level of quality expectation and must be comfortable with manual labor. In addition, QCT must have the capability to work within a team environment, take pride in the quality of their work and follow directions.

Duties & Responsibilities

• Perform daily audits of finished and in-process goods to verify plug quality.
• Perform varied inspection tasks including visual and touch point inspections and test raw materials
• Perform quality checks throughout productions runs including set-up and end of run.
• Maintain documents and record according to departmental requirements.
• Audit line cleanliness and perform post cleaning QA inspections.
• Audit cleaning records, identify deficiencies and communicate to managers.
• Maintain expertise in line cleaning procedures and auditing cleanliness of the facility.
• Create, edit, standard operating procedures for the quality department.
• Follows all Company safety policies and procedures.
• Follows Food Safety and GMPS’s as directed by Management.
• Additional duties as assigned.

Essential Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Be dynamic, ask questions, be resourceful, be ambitious.
• Excellent verbal communication skills

• Ability to work independently, as well as to collaborate in a team environment
• Strong attention to detail
• Dependable
• Ability to be at work on time and as scheduled
• Ability and willingness to learn
• Positive energy and attitude
• Ability to maintain a professional demeanor when interacting with teammates, visitors, customers & vendors

Education and Experience: The requirements listed below are representative of the knowledge, skill and/or ability required.

• Science related or laboratory related diploma or 1-2 years of relevant work experience.
• Previous manufacturing and auditing or comparative experience (preferred).
• Detail oriented and high level of quality expectation.
• Demonstrated computer skills including Microsoft Outlook and Excel.
• Ability to work in a fast-paced environment.
• Conflict resolution.

Language Skills

• Ability to read, write, and speak English;

Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• The employee must be capable of properly wearing a respirator and other applicable PPE and safety equipment, as required by the employer.
• While performing the duties of this job, the employee is regularly required to talk or hear.
• While performing the duties of this job, the employee is regularly required to use hands to handle and feel; reach with hands and arms.
• The employee is regularly required to stand, walk, twist, reach, stoop, kneel, and crouch.
• The employee must often lift and/or move product up to 50 pounds.
• Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Manufacturing environment

• The temperature will vary from hot and humid to cold, depending on the weather and location.

• Must be able to adapt to the noise level of a manufacturing setting, which is usually moderate to heavy.
• This role routinely uses standard office equipment such as a computer, phone, printer/scanner, and filing cabinets.

Job Description

Salary: $50,000 - $0,000 K

Who we are:

Response Biomedical Corp. (Response) has been transforming acute care diagnostic testing with a focus on improving patient outcomes for over 30 years. We are a Canadian-owned company that develops, manufactures and distributes immunoassays around the world. We believe the people we work with, including our partners, healthcare teams, and employees are the cornerstone of our success.

What we do:

The RAMP platform is a global leader in cardiovascular and acute care testing for the triage and diagnosis of life-threatening diseases directly from whole blood samples.
We understand the stresses associated with rapid and accurate diagnosiswhen every minute counts and we are committed to providing lab-quality results within minutes while reducing the total cost of care.

.

Who we are looking for?

We are searching for an Quality Control Specialist to join our Quality Control team that is ready for a challenge and looking to make a difference. The successful candidate will be responsible for the testing of incoming raw materials, completing in process inspections for manufacturing, and the analytical testing of components and finished products to ensure that quality standards and procedures are met and aligned with legislation and required specifications. The Quality Control Specialist is also responsible for monitoring QC specifications and metrics to identify trends in established controlled processes and procedures, for the core purpose of improving patient outcomes and saving lives globally.

Key Responsibilities:

Quality Control

• Performs testing of raw materials and independently executes ongoing product testing as part of routine batch release for RAMP products.
• Develops, executes, and maintains product stability studies to ensure labeling claims are supported for field products and new development work.
• Reviews Quality Control documents to ensure that all products meet specifications.
• Continuously reviews Quality Control data to identify trends in established controlled processes and procedures in order to initiate Corrective and Preventative Actions as required.
• Generates SOPs, test method documentation, deviation reports, investigation summaries, change control reports, and certificates of analysis.
• Assists with analytical method development and performs validation testing as required.
• Provides training as required.
• Performs laboratory housekeeping.

Manufacturing Support

• Provides technical and process direction to Manufacturing.
• Performs QVB and in-process inspections of production activities as required and provides training on these as required.

Quality Systems

• Ensures compliance with the requirements of working in a regulated environment under the guidelines set by the Company to assure adherence to its internal Quality Management System (QMS) and applicable global requirements.
• Ensures adherence to Standard Operating Procedures and Work Instructions and supports CAPAs, VRs, and NCs in accordance with the QMS.
• Supports continuous improvement of the Quality Control GMP systems and QMS.
• Conducts investigations and root cause analyses (OOSs, NCRs, CCRs) to support manufacturing troubleshooting and/or complaint handling.

Education, Work Experience, Knowledge, and Skills:

Formal Education

Post Secondary Education or Degree in Biochemistry, Chemistry, Biology, Medical Technology, Biotechnology or Related Science.

Work Experience

• Minimum 3 year of direct experience working in a regulated laboratory; experience in analytical testing/medical device industry is preferred.
• Familiar with quality management systems, ISO, FDA regulations, guidelines, and associated standards.
• Experience in health care, medical device, or similar regulated industry.

Skills & Knowledge

Must-Have :

• Proficiency with Microsoft Office productivity suite and database applications.
• High level of proficiency in Microsoft Excel skills including plotting and using formulas and regression tools.
  
• Strong technical report writing skills.
• Strong problem identification and problem resolution skills.

• Excellent time management skills and ability to multi-task; able to complete tasks with flexibility in responding to changes in direction/priorities.
• Demonstrated ability to work as part of an interdisciplinary team and independently in a professional environment.
• Strong personal alignment with the companys vision, values, and culture.
  

Nice to Have :

• Coding experience and familiarity with Microsoft Excels VBA coding and macros.

• Experience with risk management, NC/CAPA investigations, and experience working with QMS.
• Experience working in a regulated environment under the guidelines set by the Company to assure compliance with the Medical Device Single Audit (MDSAP) regulations, ISO13485, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Design Control and Workers Safety.
• Experience related to medical devices, protein biochemistry, and immunological methods.

The starting salary for this position ranges from 50,000 to 60,000 annually, depending on the candidate's experience and qualifications. Our salary structure is aligned with market standards and is finalized considering factors such as job-related expertise, skills, education, and experience.

Please note that this position is only available to candidates who are authorized to work in Canada.

*We regret that relocation will not be provided.

* While we appreciate the interest of all applicants, only those candidates selected for interview will be contacted.

We'recommitted to a diverse and inclusive workplace.We welcomeapplicants withoutregardto race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. All employment decisions are based on business needs, job requirements and individual qualifications.

Job Description

Salary:

Who We Are:

At Bronte Construction, we merge innovation with expertise to deliver quality construction projects with an ingrained environmental focus. We're proud to enhance communities, considering the impact for future generations. Our team upholds the Foundation Principles of Safety, Balance, Culture, Quality, and Character. With a workforce passionate about excellence, we foster a space where every day is an opportunity to bring our best to every site.

How We Stand Apart:

• Recognized as one of Canada's fastest-growing companies from 2016 to 2019
• Winner of the Environmental Project of the Year 2018
• COR Certified Contractor status
• Comprehensive health, dental, and vision insurance
• Generous RRSP matching for secure financial growth
• Commitment to continuous learning and career advancement

The Opportunity:

We're seeking a dedicated Quality Control Manager who will ensure the highest standards of quality across our operations. As a key player in our team, you'll be the touchstone for maintaining, implementing, and enhancing our Quality Management System, driving excellence throughout Bronte Constructions projects.

Your Role and Responsibilities:

As our Quality Control Manager, you will:

• Steer our quality assurance programs and initiatives, fostering a culture of continuous quality enhancement.
• Serve as a liaison between contractors and key stakeholders to uphold quality-related matters.
• Conduct systematic management reviews and quality audits, ensuring compliance and operational excellence.
• Command the quality landscape, leveraging your ISO 9001 Lead Auditor expertise to maintain our distinguished quality benchmarks.
• Champion our Quality Management System, orchestrating its robust functioning and adherence to industry standards.

A Day with Bronte:

• Full engagement with the Contractors corporate management team to align and optimize quality processes.
• Devising and coordinating Quality Audit Plans, ensuring seamless operations across various projects.
• Spearheading quality control and assurance strategies from initiation to implementation.
• Streamlining communication channels for effective quality discussions and decisions.
• Pioneering strategic improvements through analysis and meticulous attention to detail.

Who You Are:

• A degree holder in engineering, architecture, or a related discipline from a reputed university or college.
• At least 2 years of experience as a Quality Control Coordinator with a track record in the construction industry.
  
• ISO 9001 Lead Auditor Course graduate, ready to leverage your knowledge for the betterment of our quality practices.

Brontes Promise:

By joining us, youre not just taking on a role but becoming an integral part of a legacy. Here, your efforts are recognized, your skills honed, and your contributions celebrated.

Ready to shape the quality of constructions that stand the test of time? Apply to become the cornerstone of Bronte Constructions commitment to quality. We cant wait to build the future with you.

Job Description

Join us and build what matters for BC.

Jacob Bros Construction is now hiring a Quality Control Manager  to manage activities at our CSA Precast facility, and ensure ready mix batch plant mixes meet CSA standards and certifications for major projects throughout the lower mainland.

Mandatory Requirements:

• Diploma in Civil Technology; Bachelor’s Degree in Civil Engineering or a related discipline
• Currently located in the lower mainland
• Able to work full-time effective immediately 
• Valid driver's license and ability to commute to sites throughout the lower mainland 

• Samples and tests concrete
• Records and reports results; maintains quality files
• Liaises with clients and site personnel
• Works with trade and area supervisors to improve in-process quality
• Troubleshooting real time compliance issues in the field
• Monitors non-compliance protocols
• Performs additional duties as assigned

• Diploma in Civil Technology, Bachelor’s Degree in Civil Engineering or a related discipline
• Minimum of 5-10 years Quality Control experience
• Ability to communicate effectively with project teams and subtrades 
• Strong English communication skills, both verbal and written
• Legally entitled to work for any employer in Canada

• Competitive compensation packages
• Group Medical, Extended Health and Dental Plan
• Matched RRSP contribution
• Eligibility for Profit Sharing Program
• Three weeks vacation
• New 50,000 square foot office and maintenance facility in South Surrey with full gym and on-site personal trainer
• 5 Year Service Award (Trip for two anywhere in North America)
• Eligibility for $2000 Referral Bonus Program

Job Description

Salary:

Job Description:

The Quality Control Auditor reports to the Quality Control Lead.

The Quality Control Auditor ensures that quality assurance is in accordance with expectations set out in the Quality Manual, Quality Procedures and Work Instructions and is equal to the requirements in the customer order or customer contract or the ISO9001:2015 & AS9100:D Standards. The Quality Control Auditor provides leadership in quality issues.

Knowledge, Skills & Abilities:

• Performs on Machine quality auditing for first off inspections.
• CMM operation proficiency is mandatory.
• CMM beginner programming experience is a must: Calypso
• Master proficiency reading blueprints, mechanical drawings, GD&T specifications and measuring features & characteristics in physical components to verify & validate its conformance by using metrology instruments (durometers, bore/profile/high/roughness, angle/radius gauges, micrometers, dial indicators, Gage maker, mic track, optical-laser scanning probing arms, etc.).
• Proficient in both measuring units systems: Imperial & International System of Units (SI).
• Master proficiency measuring element by element API Tubing & Casing (T&C) and Rotary Shouldered Connections (RSC) threads.
• Verifies & validates processes and product conformance via Inspection Receiving, First Offs, Final Inspection, Process & Dock audits, testing.
• Identifies and records non-conformances and participates with the multidisciplinary team to identify Root Cause, Corrective & Preventive Actions.
• Submits recommended solutions to Quality problems and Manufacturing issues.
• Verifies correction of nonconforming items. Controls further processing of nonconforming items until the deficiency or unsatisfactory conditions have been resolved.
• Ensures that personnel understand inspection procedures and are fully qualified to perform these inspections.
• Prepares inspection records required in advance so that inspections can be processed in a timely and efficient manner.
• Ensures that personnel carry out inspections and testing according to stated procedures.
• Collects, inspects, and maintains all quality records & statistical data for accuracy.
• Maintains inspection/test equipment and ensures that it is accurate and calibrated to stated procedures.
• Ensures corporate assets and property are actively protected and safeguarded and liabilities and errors are minimized.
• Other duties as directed by Quality Control Lead.

Key Standards for Role:

• AS9100:D
• ISO 9001:2015
• ISO 10012:2003
• IATF 16949-2016

Qualifications & Requirements:

• 
  5+ years of experience as Quality Control Auditor in a manufacturing environment preferred
• 
  Engineering designation preferred.
• 
  Bachelor of Engineering degree (4+ years) advantageous

Job Description

Come join an expanding business in Halifax as their Quality Control Clerk

In this role you will:

Review and audit all customized clients orders.
Assess proper inventory levels
Work as a liaise between the warehouse and the Customer Service Department

Looking for a detailed and professional person with strong communication and teaming abilities and a natural problem-solver.

This is a FT role on the Halifax side of HRM. Not on a bus route. Benefits and vacation.

Reach out to Paul Melancon at