Chemistry Senior Analyst, Quality Control

Groupe Parima; Brossard; On-site; CAD 70,000 - 90,000; Full time

Job summary

A Contract Development and Manufacturing Organization is seeking a Chemistry Senior Analyst, Quality Control. Responsibilities include conducting chemical analyses, ensuring data quality, and training new employees. The ideal candidate has a DEC or Bachelor's in Science, with at least 5 years of quality control experience in the pharmaceutical industry and knowledge of GMP regulations. This role offers various employee benefits including a recognition program and accessible transport.

Benefits

Recognition program and social activities

Personal days

Employee assistance program

Accessible by public transit or free parking

Referral program

Qualifications

• Minimum of 5 years of experience in quality control within the pharmaceutical industry.
• Knowledge of Canadian GMP (Health Canada) and US FDA regulations.
• Experience with laboratory investigation guidelines.

Responsibilities

• Perform analyses of finished products and raw materials according to methods.
• Ensure integrity and quality of data in the QC laboratory.
• Participate in employee training and maintain equipment records.

Skills

Quality control expertise

GMP knowledge

HPLC experience

GC experience

Training ability

Education

Diploma of College Studies (DEC) or Bachelor's in Science

Job description

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 25 years, we have developed expertise in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. https://www.groupeparima.com

Chemistry Senior Analyst, Quality Control

Positions Available:

1. Day shift
2. 12-hour weekend shift (Friday, Saturday, and Sunday)

The Chemistry Senior Analyst conducts chemical and physical analyses in the laboratory according to an established schedule, following specifications, methods, procedures, and Good Manufacturing Practices (GMP). The analyst also serves as a resource person for the team.

Responsibilities:

• Perform analyses of finished products, bulk materials, raw materials, and stability samples according to current methods.
• Ensure the integrity and quality of data in the QC laboratory.
• Assist and participate in employee training.
• Track calibration and maintenance of laboratory instruments.
• Maintain equipment records, standards, and manage reagent, standard, and consumable inventories.
• Participate in investigations, problem-solving, and development of R&D methods.
• Write and review procedures related to the QC laboratory.
• Participate in the development and validation of new analysis methods.

Skills and Experience Required:

• Diploma of College Studies (DEC) or Bachelor's degree in Science (Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline).
• Minimum of 5 years of experience in quality control within the pharmaceutical industry.
• Knowledge of Canadian GMP (Health Canada) and US FDA regulations.
• Knowledge of laboratory investigation guidelines (FDA OOS/OOT investigations, MHRA).
• Familiarity with Pharmacopoeias (USP, Ph. Eur., BP) and their laboratory applications.
• Experience with techniques such as HPLC (UPLC) and GC.
• Ability to train new employees.

What We Offer:

• Recognition program and social activities
• Personal days
• Employee assistance program and online medical services
• Accessible by public transit or free parking
• Referral program