Analyst, Quality Control

Help us build the health of tomorrow

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

Weekdays: Friday, Saturday, and Sunday
Schedule: 12-hour shifts

• Effectuer de façon autonome les analyses chimiques et physiques selon l’horaire établi en suivant les spécifications, méthodes et procédures BPF chez Groupe PARIMA.

• Contributes to laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.

• Perform all duties in compliance with health and safety regulations and report any identified health and safety risks to supervisors.

Responsibilities

• Independently and proficiently perform testing of finished products, bulk products, raw materials, and stability samples according to approved methods.

• Critically evaluate analytical results while ensuring compliance with established procedures and standards.

• Enter analytical results into the Laboratory Information Management System (LIMS), using sound judgment and comparing results against historical trend data.

• Ensure the integrity and quality of Quality Control laboratory data.

• Assist with and participate in the training of junior analysts.

• Perform maintenance and calibration of assigned laboratory instruments within established timelines.

• Help maintain inventories of reagents, solvents, and laboratory consumables required for testing and laboratory operations.

• Prepare laboratory investigation reports and actively participate in investigations.

• Contribute to problem-solving initiatives and continuous improvement activities within the laboratory.

• Follow health and safety procedures and report any health and safety risks to supervisors.

• Occasionally perform certain Senior Analyst duties during absences.

• Carry out any other tasks required to support the efficient operation of the laboratory.

Required qualifications and experience

• College diploma (DEC) in Science (Chemistry, Biochemistry) or a related discipline.

• Minimum of five (5) years of Quality Control experience in the pharmaceutical industry.

• Knowledge of Canadian Good Manufacturing Practices (GMP) and Health Canada requirements.

• Knowledge of pharmacopeias (USP, Ph. Eur., and BP) and their application in a laboratory environment.

• Strong teamwork and collaboration skills.

• Ability to train and mentor junior personnel.

• Strong sense of initiative.

• Excellent communication skills.

• Proficiency with computer applications, including Microsoft Office and Outlook.

• Bilingual in French and English.
  

What we offer

• Group retirement savings plan

• Employee recognition program and social activities

• Personal days

• Employee Assistance Program and telemedicine services

• Complimentary hot  beverages (hot chocolate, coffee, and mocha)

• Easy access by public transit or free parking

• Employee referral program

• Subsidized meal program

• The use of the masculine gender is intended solely to simplify the text and facilitate readability.
  

The use of the masculine gender is intended solely to simplify the text and facilitate readability.