Product Development Associate
Groupe ParimaMontreal, Quebec30+ days ago
Job descriptionDEC 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. Flexible work schedule 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 Subsidized meal program
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 :
What we offer :
Additional information :
Employment type : Full-time