QA Specialist Eurofins Experchem Laboratories, Inc.

Eurofins Experchem Laboratories Inc. is seeking a detail-oriented and analytical QA Specialist to join our team in Toronto Canada. As a QA Specialist you will play a crucial role in ensuring the quality and integrity of our laboratory testing processes contributing to our commitment to excellence in the chemical and pharmaceutical testing industry.

• Review and determine status of the quality Documents (including but not limited to validation studies mapping studies calibration reports);
• Upload maintain and update quality documentation in D4 platform (or any other active platform used by laboratory at the time);
• Assist laboratory management in managing and completing Proficiency Testing program. Activities include but are not limited to: scheduling ordering data entry investigations;
• Generate verification and validation/ Calibration documents (including but not limited to calibration reports qualification and requalification documents);
• Generate protocols and reports for Qualification temperature mapping;
• Log and review complaints; compile required ISO 17025 documents for the evaluation of complaints;
• Assist with self-inspections (method audits horizontal audits);
• Assist with the ongoing tracking and maintenance of ISO 17025 documents;
• Review and approve daily weekly monthly a.o. production related quality documents (logs forms such as but not limited to: balance verifications media quality documents testing related forms etc.);
• Support the training of new staff;
• Prepare perform and write qualification (OQ/PQ) protocols for instrumentation;
• Prepare perform and write Calibration procedures;
• Ensure laboratory instruments are calibrated on time;
• Maintain equipment associated documentation and records (calibration verification qualification maintenance a.o.);
• Assist laboratory staff in contacting contractors for outside PM and instrument repairs;
• Evaluate and summarize instrumentation qualification data in final reports;
• Temperature monitoring deviation investigations and record keeping;
• Attend to the monitoring system alarms (non-conformance investigation advising management team assisting in corrective action implementation);
• Review training records and update training documentation (on paper or in LearnUpon);
• Initiate and conduct deviations and out-of-specification investigations (non-conformances);
• Initiate and conduct Corrective Action and Preventative Action (CAPA) investigations;
• Initiate and assist Change Control procedures;
• Adhere to the Standard Operating Procedures;
• Circulate Standard Operating Procedures and follow up on training requirements;
• Ensure that all staff members are following the Standard Operating Procedures at all times;
• Assist with the maintenance of ISO 17025 accreditation;
• Attend staff meetings;
• Any other duties as delegated by management (currently assist in reporting results eLIMS-BPT).

Qualifications :

• Bachelors degree in Chemistry Biochemistry or a related scientific field
• Minimum of 2-3 years of experience in quality assurance within a laboratory environment
• Strong knowledge of quality assurance methodologies and laboratory testing procedures
• Proficiency in data analysis interpretation and reporting
• Experience with laboratory information management systems (LIMS)
• Familiarity with regulatory standards such as ISO GMP and GLP
• Excellent attention to detail and strong analytical skills
• Ability to work efficiently and maintain organization in a fast-paced environment
• Effective communication and interpersonal skills
• Experience with chemical or pharmaceutical testing preferred
• Quality Assurance certifications (e.g. ASQ) are a plus
• Understanding of chemical and pharmaceutical testing processes
• Familiarity with regulatory requirements in the laboratory industry

WORKING CONDITIONS

• This position is in an office/lab hybrid environment where most of the time will be sitting at a desk working on a computer. Hazardous materials are handled using established safety procedures and appropriate PPE.
• Shift work and overtime may be required as well as working periodic weekends and/or evenings.

Additional Information :

At Eurofins we offer excellent full-time benefits including health & dental coverage life and disability insurance RRSP with 3% company match paid holidays paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process or those needing job postings in an alternative format may e-mail a request via the website at .

As a Eurofins employee you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins please explore our website at 

We thank all applicants within commuting distance of GTA Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES CALLS OR EMAILS PLEASE

Remote Work :

No

Employment Type :

Full-time