Chemistry Senior Analyst, Quality Control

Groupe Parima; Laval; On-site; CAD 60,000 - 90,000; Full time

Job summary

A Contract Development and Manufacturing Organization is looking for a Chemistry Senior Analyst in Laval, Quebec. The role involves conducting laboratory analyses and maintaining data integrity. Candidates should have a DEC or Bachelor's degree in a related field and at least 5 years of experience in quality control in the pharmaceutical sector. The position offers various benefits, including medical and dental plans, as well as a retirement plan.

Benefits

Medical – dental & travel benefits

Group retirement plan

Recognition program & social activities

Employee assistance program & online medical service

Hot Beverages

Accessible by public transit or free parking

Referral program

Qualifications

• Minimum of 5 years of experience in quality control in the pharmaceutical industry.
• Knowledge of Canadian and American Good Manufacturing Practices.
• Familiarity with laboratory investigation guides and pharmacopoeias.

Responsibilities

• Carry out analyses of finished products and raw materials.
• Ensure the integrity and quality of data at the QC laboratory.
• Assist and participate in the training of employees.

Skills

Knowledge of GMP

HPLC (UPLC) and GC techniques

Skills for training new employees

Education

Diploma of College Studies (DEC) or Bachelor in Science

Job description

Groupe PARIMA is aContract Development and Manufacturing Organization (CDMO), established in 1994. For over 25 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

Chemistry Senior Analyst, Quality Control

1 Position : Day shift

1 Position : 12 hour weekend shift (Friday, Saturday and Sunday)

The Chemistry Senior Analyst carries out chemical and physical activities at the laboratory according to the schedule established by following the specifications, methods, procedures and good Manufacturing Practices (GMP). The Analyst also acts as a resource person for the team.

Responsabilites :

• Carry out the analyses of finished products, bulks, raw materials and stability according to the methods in force
• Ensure the integrity and quality of data at the QC laboratory
• Assist and participate in the training of employees
• Track interviews or calibrations of all laboratory instruments
• Maintaining equipment records, standards and maintaining reagent, standard and / or consumables inventory
• Participate in investigations, problem solving and the development of R&D methods
• Write and review procedures related to the QC laboratory
• Participate in the development and / or validation of new analysis methods

Skills and Experience required :

Diploma of College Studies (DEC) or a Bachelor in Science (Chemistry, Biochemistry, Pharmaceutical Program, or a discipline related)

Minimum of 5 years of experience in quality control in the pharmaceutical industry

Knowledge of Canadian Good Manufacturing Practices (GMP) (Health Canada) and American (FDA)

Knowledge of laboratory investigation guides (FDA guidance to OOS and OOT investigations, MRHA)

Knowledge of Pharmacopoeias (USP, Ph. Eur. and BP) and their applications within a laboratory

Knowledge with the following techniques : HPLC (UPLC) et GC

Skills for training new employees

What we're offering :

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

Location : 4450 Cousens St., Montreal, QC, Canada, H4S 1X6