- Prepare and execute lab-scale batches
- Assist formulators with documentation and execution of batches
- Conduct equipment cleaning assessment and validation
- Write protocols and reports for cleaning activities
- Coordinate analytical work with laboratories
- Oversee manufacturing and packaging processes
- Participate in creating necessary forms, procedures, and batch records
- Manage inventory of the laboratory
- Support other product development activities
- DEC or Bachelor's degree in Science
- Minimum of 1 year experience in a cGMP pharmaceutical setting
- Practical experience in dosage forms and process development
- Formulation experience is a plus
- Strong knowledge of GMP, GLP, Safety, and FDA guidelines
- Detail-oriented with good interpersonal and communication skills
- Proficient in technical writing and problem-solving
- Knowledge of Process Safety concepts
- Ability to lead, assist in training, and adapt to schedules
- Flexible work schedule
- Medical, dental, and travel benefits
- Retirement plan
- Recognition program and social activities
- Personal days
- Employee assistance and medical services
- Hot Beverages (Coffee, Hot chocolate, Mokaccino)
- Accessible by public transit or free parking
- Referral program
- Subsidized meal program
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Product Development Associate - Laval, Canada - Groupe Parima
Description
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 25 years, we have built a strong expertise in developing and manufacturing non-sterile liquids, suspensions, and semi-solid pharmaceutical products.
Position: Product Development Associate
The role of a product development associate involves providing hands-on support for product development activities within projects and commercial products.
Responsibilities:
Skills and Experience Required:
Benefits: