Senior Analytical Chemist
2 weeks ago
Taro Pharmaceuticals Inc. is a multinational, specialty pharmaceutical company with a vision of reaching people and touching lives globally as a leading provider of valued medicines. We are dedicated to meeting the needs of our customers and the overall community through the innovation, development, manufacturing, and marketing of the highest quality healthcare products. Established in [Year], Taro’s world-class production facility is located in Brampton, Ontario, with a current team of over [Number] Canadian employees. Our company’s focus on the dermatology sector has made us a leading manufacturer and supplier of specialized topical products with a diverse portfolio of creams, ointments, liquids, and gels. With support from our parent company, Sun Pharma, one of the world’s largest specialty generic pharmaceutical companies, we are committed to providing a healthy, safe, and rewarding environment for all of our employees. Our reward packages have been designed to meet the needs of our diverse workforce and their families. For additional information, visit [Website].
What we offer:- A safe and clean; GMP regulated work environment
- Opportunities for career growth and development
- A competitive wage/salary
- Employee training and organizational development programs, internal mobility programs, and employee recognition programs
Job Purpose: The main responsibilities of this position are to develop and validate analytical test methods and provide analytical support to product development chemists. Key duties include development and validation of new analytical methods, preparation of protocols and reports, and other documents for regulatory submissions. Testing of R&D batches, raw materials, and packaging components in accordance with GMP/GLP regulations may be required as needed. Work is completed with little supervision/guidance in a timely manner. Participate in the training/coaching of new staff.
Duties and Responsibilities:- Perform testing using advanced GC/HPLC techniques as well as specialized testing using particle size analysis and other techniques as required
- Develop, validate, and document new analytical methods with minimum supervision. Independently prepare method validation protocols, method development, and method validation reports
- Research and prepare drug product and drug substance specifications
- Perform compendial method verifications and validations as per protocol
- Perform testing of R&D products and raw materials as per specifications
- Participate in activities leading to product approval under the guidance of Senior R&D staff (i.e., deficiency letter responses for chemistry issues, investigations, etc.)
- Function as the Analytical Project Lead for select development projects
- Conduct laboratory investigation activities (OOS, laboratory incidents, etc.)
- Report and clearly document all research work performed
- Report GMP work in accordance with current GMP/GLP regulations
- Initiate and follow through with actions required for change controls
- Complete Corrective and Preventative Actions (CAPA’s)
- Participate in the training of new staff
- Maintain a clean laboratory environment and ensure that safety regulations are followed
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