Product Development Associate

1 month ago

Montreal, Quebec, Canada Groupe Parima Full time
Product Development Associate

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO) with over 25 years of experience in developing and manufacturing non-sterile liquids, suspensions, and semi-solid drug products.

Job Summary:

The Product Development Associate provides hands-on support to product development activities associated with product development projects and commercial products. This role involves preparing and executing lab-scale batches, providing support to formulators, and performing swabbing for equipment cleaning assessment and cleaning validation.

Responsibilities:

  • Prepare and execute lab-scale batches in accordance with cGMP guidelines.
  • Provide support to formulators with documentation, preparation, and execution of lab-scale batches.
  • Perform swabbing for equipment cleaning assessment and cleaning validation.
  • Write protocols and reports for cleaning assessment and cleaning validation activities.
  • Coordinate analytical works with chemistry and microbiological laboratories.
  • Provide on-the-floor oversight of manufacturing and packaging processes as necessary.
  • Participate in drafting 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.

Requirements:

  • 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:

  • Flexible work schedule.
  • Medical, dental, and travel benefits.
  • Group retirement plan.
  • Recognition program and social activities.
  • Personal days.
  • Employee assistance program and online medical service.
  • Hot beverages (hot chocolate, coffee, Mokaccino).
  • Accessible by public transit or free parking.
  • Referral program.
  • Subsidized meal program.

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