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Product Development Associate

2 months ago

Laval, Quebec, Canada Groupe Parima Full time
{"title": "Product Development Associate", "description": "Join Our Team at Groupe Parima

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.

As a Product Development Associate, you will play a key role in supporting product development activities, working closely with our team to ensure the successful launch of new products.

Key Responsibilities:
  • Prepare and execute lab-scale batches to support product development projects.
  • Collaborate with our formulator to prepare and execute lab-scale batches, ensuring accurate documentation and execution.
  • Perform swabbing for equipment cleaning assessment and cleaning validation, ensuring compliance with regulatory requirements.
  • Write protocols and reports for cleaning assessment and cleaning validation activities, ensuring accuracy and attention to detail.
  • Coordinate analytical works with chemistry and microbiological laboratories, ensuring timely and accurate results.
  • Provide on-the-floor oversight of manufacturing and packaging processes, ensuring compliance with GMP and regulatory requirements.
  • 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 inventory management of PDS laboratory.
  • Provide support to other product development production activities, ensuring seamless collaboration and communication.
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.
"}