Product Development Associate

Groupe Parima; Montreal; On-site; CAD 55,000 - 75,000; Full time

Job summary

A leading Contract Development and Manufacturing Organization in Montreal seeks a Product Development Associate. The role entails providing hands-on support for product development activities, maintaining compliance with GMP regulations, and coordinating laboratory activities. The ideal candidate holds a relevant degree and has experience in a cGMP environment, demonstrating excellent communication skills and a detail-oriented approach.

Benefits

Recognition program & social activities

Personal days

Employee assistance program & online medical service

Accessible by public transit or free parking

Referral program

Qualifications

• Minimum of 1 year experience in a cGMP pharmaceutical environment.
• Some practical experience in semi-solid dosage forms.
• Bilingual in English and French.

Responsibilities

• Prepare and execute lab-scale batches.
• Write protocols and reports for cleaning validation activities.
• Coordinate analytical works with chemistry and microbiological laboratories.

Skills

Dynamic and multitasking ability

Good interpersonal and communication skills

Strong problem solving

Technical writing

Proficient in Process Safety concepts

Good working knowledge of GMP

Detail oriented

Education

DEC or Bachelor’s degree in Science

Job description

Groupe PARIMA is a Contract 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 / fr /

Product Development Associate

The product development associate provides hands-on support to product development activities associated with product development projects and commercial products.

Responsibilities :

• Prepare and execute lab-scale batches.
• Provide support to formulator with documentation, preparation and execution of lab-scale batches.
• Perform swabbing for the equipment cleaning assessment and cleaning validation.
• Write protocols and reports for the cleaning assessment and cleaning validation activities;
• Coordinate the analytical works with chemistry and microbiological laboratories.
• Provide on-the-floor oversight of the manufacturing and packaging processes, as necessary.
• Participate in the drafting of forms, procedures, manufacturing and packaging batch records, protocols and reports necessary for the proper functioning of the PDS department.
• Coordinate and support the inventory Of PDS laboratory
• Provide support to other product development production activities.

Skills and experience required :

• DEC or Bachelor’s degree in Science (Chemistry, or related technical / scientific field), from a Canadian University, or an equivalent scientific diploma recognized by a Canadian University or an accredited Canadian organism.
• Minimum of one (1) year of experience in a cGMP pharmaceutical environment.
• Some practical experience in semi-solid dosage forms and / or process development and / or cleaning assessment,
• Experience in formulation (Asset)
• Dynamic and multitasking ability
• Good working knowledge of GMP, GLP, Safety and FDA guidelines,
• Very organized and detail oriented, with a strong focus on accurateness,
• Good interpersonal and communication skills (both in English and French; written and spoken),
• Strong problem solving, technical writing,
• Proficient in Process Safety concepts and methodology,
• Able to lead and assist in training others,
• Able to be flexible and adapting to process schedules.

What we offer :

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

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