Benefits
- Dental insurance
- Employee assistance program
- Free parking
- Medical and paramedical expenses coverage
- Paid sick leave
- Registered retirement savings plan
- Travel Assistance
- Salary To be discussed
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Full time
-
Permanent job
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Day ,Weekend shift work
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Published since 1 day(s)
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2 positions to fill as soon as possible
Description
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
Two positions to fill:
- Day: Monday to Friday (40 hours per week)
- Weekend: Friday, Saturday and Sunday (12 hours per day)
The Quality Control Analyst...
Responsibilities:
- Independently perform chemical and physical analyses according to the established schedule, following Groupe Parima's specifications, methods, procedures and Good Manufacturing Practices (GMP).
- Participate in laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.Work in compliance with health and safety rules and report health and safety risks to supervisors.
- Good knowledge of the 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 tests by volumetric and automatic titration
- Independently perform UV-Visible spectrophotometer tests.
- Prepare mobile phases, diluents and dissolution media.
- Independently perform dissolution, assay and related substances tests by HPLC.
- Analyze results critically and with concern for compliance with the standards set by current procedures.
- Enter analytical results in the LIMS using sound judgment by comparing them with trend analyses.
- Ensure data integrity and quality in the QC laboratory.
- Assist and participate in the training of junior analysts.
- Perform maintenance or calibration of laboratory instruments used in physical tests.
- Help maintain inventories of reagents, solvents and consumables required for analyses or for the proper operation of the laboratory.
- Actively participate in laboratory investigations.
- Participate in laboratory problem solving and continuous improvement.
- Follow health and safety rules and report health and safety risks to supervisors.
- Occasionally cover certain senior analyst tasks based on operational needs.
- Any other tasks required for the proper operation of the laboratory.
Work environment
Requested skills
Skills and experience required:
- College diploma (DEC) in Science (Chemistry, Biochemistry) or a related field, with 3 years in a similar position.
- Bachelor’s degree in science (Chemistry, Biochemistry) with 2 years in a similar position
- Quality Control experience in the pharmaceutical industry
- Knowledge of Canadian Good Manufacturing Practices (GMP) (Health Canada)
- Knowledge of pharmacopoeias (USP, Ph. Eur. and BP) and their application in a laboratory
- Teamwork and collaboration skills
- Shows initiative
- Good communication skills
- Good computer skills (Microsoft Office, Outlook)
- Bilingual (French and English)
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.
Requirements
Level of education
College
Diploma
DEC
Completed
Work experience (years)
0-2 years
Written languages
Fr : Intermediate
En : Intermediate
Spoken languages
Fr : Intermediate
En : Intermediate
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