Formulator, Product Development
at Taro Pharmaceuticals INC Canada
Brampton, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Oct, 2024 | Not Specified | 19 Jul, 2024 | N/A | Gmp,Communication Skills,Pharmaceutical Sciences,Design,Word Processing | No | No |
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Description:
QUALIFICATIONS
- Good theoretical and practical knowledge of liquid and semi-solid formulation development.
- Hands on experience and skills of design, implement and evaluate experiments.
- A good understanding of GMP
- Familiarity with Microsoft word processing and spreadsheet programs
- Ability to work effectively in a team-based environment.
- Good organizational skills and multi-tasking skills to facilitate the timely completion of projects.
- Good written and verbal communication skills
- Ph. D. or a M. Sc. degree in Pharmaceutical Sciences with minimum one-year experience in formulation development is preferred for this position, or a B.Sc. or community college degree with 3 years experience in Semi-Solid and Liquid formulation development.
- Utilize and apply basic scientific knowledge and semi-solid theories to design effective experiments.
- Evaluate and assess formulations and processes based on analytical results
- Collaborate with manager team and other R&D professionals, plant staffs, administration staffs effectively to solve any issues or conflicts during product development
PHYSICAL REQUIREMENTS
Office based role
Responsibilities:
JOB PURPOSE
The purposes of the position are to develop the formula and process for new products in accordance with GMP/GLP and Taro procedures, work is completed in timely manner to ensure meeting departmental and corporate goals.
DUTIES AND RESPONSIBILITIES
Develop formulae and process for new products
- - this includes literature searching, sourcing new raw materials and packaging components, preparing lab scale developmental batches, designing and executing experiments to support the final formulation and process.
- Write Master Formula and Packaging Work Orders for Exhibit Batches and Facilitate manufacturing and the packaging of exhibit batchesReport and clearly document all research work are performed
- - this includes documentation of protocol, experimental process, problems and observations and formulation development report.
- Participate in activities leading to Technical Transfer, process validation and commercial production troubleshooting under the guidance of Senior Associate/Manager
- Plan project development activities proactively, and update outcomes and completion of the activities in a timely manner
- Maintain a clean laboratory environment and ensure that safety regulations are followed
- Other activities to comply with GMP/GLP requirement
- Complete GMP training for updated SOPs, and complete all GMP activities and documentation correctly and in a timely manner.
- Other duties as assigned.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
Brampton, ON, Canada