Quality Control Analyst - Weekend Shift

Groupe PARIMA has been a contract development and manufacturing company since 1994. Over the years, we have developed expertise in non-sterile pharmaceutical products in liquid, semi-solid, and suspension dosage forms.

• Independently perform chemical and physical analyses according to the established schedule, in compliance with Groupe PARIMA’s specifications, methods, procedures, and Good Manufacturing Practices (GMP).
• Participate in the maintenance of the laboratory and its instruments, the management of reagents and inventories, and the training of junior analysts.
• Work in accordance with health and safety rules and report health and safety risks to supervisors.

The Quality Control Analyst
…

• Independently and proficiently perform analyses of finished products, bulk products, raw materials, and stability samples in accordance with current methods.
• Critically assess results and ensure compliance with the standards established by current procedures.
• Enter analytical results into the LIMS using sound judgment and compare them with trend analyses.
• Ensure the integrity and quality of data in the Quality Control laboratory.
• Assist with and participate in the training of junior analysts.
• Perform the maintenance or calibration of all assigned laboratory instruments within the prescribed timelines.
• Help maintain inventories of reagents, solvents, and consumables required for analyses and the proper operation of the laboratory.
• Draft and actively participate in laboratory investigations.
• Participate in laboratory problem-solving and continuous improvement initiatives.
• Follow health and safety rules and report health and safety risks to supervisors.
• Occasionally perform certain Senior Analyst duties during absences.
• Perform any other duties required for the proper operation of the laboratory.

• Diploma of College Studies (DEC) in science (chemistry, biochemistry) or a related field.
• At least five (5) years of Quality Control experience in the pharmaceutical industry.
• Knowledge of Canadian Good Manufacturing Practices (GMP) requirements (Health Canada).
• Knowledge of the USP, Ph. Eur., and BP pharmacopoeias and their application in a laboratory setting.
• Strong teamwork and collaboration skills.
• Ability to train junior staff.
• Demonstrated initiative.
• Good computer skills, including Microsoft Office and Outlook.
• Bilingual in French and English.

• Medical, dental, and travel insurance.
• Group retirement savings plan.
• Employee recognition program and social activities.
• Personal days.
• Employee assistance program and telemedicine services.
• Complimentary beverages (hot chocolate, coffee, and mochaccino).
• Accessible by public transit or free parking.
• Employee referral program.

Our company operates in an international business environment, and proficiency in English is required in order to communicate effectively with suppliers and clients.