Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 30 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products. https://www.groupeparima.com/fr/

Quality Control Analyst

- Independently perform chemical and physical analyses according to the established schedule, following specifications, methods, procedures, and Positive Manufacturing Practices (GMP) at Groupe Parima.
- Participate in laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.
- Work in compliance with health and safety regulations and report health and safety risks to management.

The Quality Control Analyst is responsible for ensuring that all testing activities are performed accurately, efficiently, and in compliance with GMP requirements.

Responsibilities

- Good knowledge of USP and EP/BP Pharmacopoeias.
- Independently perform the following physical tests: pH, density, specific gravity, viscosity, deliverable volume, particle size, particle size distribution (PSD), and loss on drying.
- Independently perform assay testing using manual and automated titration methods.
- Independently perform testing using UV-Visible spectrophotometry.
- Prepare mobile phases, diluents, and dissolution media.
- Independently perform dissolution, assay, and related substances testing using HPLC.
- Analyze results with critical thinking and ensure compliance with established procedures and standards.
- Enter analytical results into the LIMS using sound judgment and by comparing them against trending data.
- Ensure data integrity and quality within the QC laboratory.
- Assist in and participate in the training of junior analysts.




- Perform maintenance and calibrations of laboratory instruments used in physical testing.
- Participate in maintaining inventories of reagents, solvents, and consumables required for analyses and laboratory operations.
- Actively participate in laboratory investigations.
- Contribute to problem-solving activities and continuous improvement initiatives within the laboratory.
- Follow health and safety regulations and report health and safety risks to management.
- Occasionally perform selected Lead Analyst tasks based on operational needs.
- Carry out any other duties required for the efficient operation of the laboratory.

Skills and Experience Required

- College Diploma (DEC) in Science (Chemistry, Biochemistry) or a related discipline, with 3 years of experience in a similar role.
- Bachelor’s Degree in Science (Chemistry, Biochemistry) with 2 years of experience in a similar role.
- Experience in Quality Control within the pharmaceutical industry.
- Knowledge of Canadian Good Manufacturing Practices (GMP) regulations (Health Canada).
- Knowledge of pharmacopoeias (USP, Ph. Eur., and BP) and their application within a laboratory environment.
- Strong teamwork and collaboration skills.
- Self-motivated with a strong sense of initiative.
- Good communication skills.
- Good computer skills (Microsoft Office, Outlook).
- Bilingual in English and French.

What we offer:

- Medical – dental & travel benefits

- Group retirement plan
- Recognition program & social activities

- Personal days
- Employee assistance program & online medical service
- Hot Beverages (Hot chocolate, Coffee, Mokaccino)
- Accessible by public transit or free parking

- Referral program

- Subsidized meal program
- Our company operates in an international business environment, and proficiency in English is required to communicate with suppliers and clients.

📌 Quality Control Analyst (Montreal)
🏢 Groupe Parima
📍 Montreal