Supervisor, Quality Control Development
4 weeks ago
**Title**:Supervisor, Quality Control Development**:
- Date: May 27, 2024- Location: Taro Pharmaceauticals CAN- Company: Taro Pharmaceuticals INC, CanadaTaro Pharmaceuticals 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 1950, Taro’s world class production facility is located in Brampton, Ontario, with a current team of over 600 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.
Taro Pharmaceuticals 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 1950, Taro’s world class production facility is located in Brampton, Ontario, with a current team of over 600 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.
**What we offer**:
A safe and clean; GMP regulated work environment
Opportunities for career growth and development
A competitive wage/salary
Incentive bonus programs that are designed to reward employees for their individual contributions
Benefit programs designed to support our employees and their families, including a comprehensive health & dental benefits package, group RRSP matching program, direct access to healthcare and well-being programs, and paid time off
Employee training and organizational development programs including tuition reimbursement, internal mobility programs, and employee recognition programs
**Job purpose**
The main responsibility of this position is to lead and mentor staff, establish and maintain the quality control systems and processes for assessing and qualifying alternate vendors for materials (API, Raw Materials and Packaging Components) to meet Health Canada and FDA regulations. This position will provide full quality control reports (Vendor Assessment in regards to analytical specifications, analytical validations and product assessment in reference to Residual Solvent Requirements, Elemental Analysis Requirements and Nitrosamines) to assist in the qualification of new vendors, in a GMP manner and according to all approved procedures. This position promotes right first time quality achievement in their lab and support lab investigations, ensuring their completeness/robustness, while ensuring their timely closure.
**Duties and responsibilities**
- Supervise, lead and mentor staff including ongoing coaching, performance feedback and reviews, routine meetings, standard hours, collaboratively identifying objectives and career development
- Ensure staff are working in a safe environment and are complying with safety procedures at all times
- Responsible for overall day-to-day operation of the lab
- Plan, schedule, organize and monitor workload optimally to ensure all operations and tasks are performed within required turnaround time metrics and adherence to set schedules, accommodating testing requirements and meeting departmental goals
- Author risk assessments and reports for Nitrosamines, Elemental Analysis and Residual Solvents evaluations
- Act as the Lab Manager back up if needed
- Investigate and documents discrepancies where required.
- Provide troubleshooting of test method and equipment issues.
- Responsible for full-cycle internal lab investigations, including trending and preventative actions.
- Work closely with and perform follow-ups with Purchasing, Vendor(s), Materials Management, Warehouse, R & D and the QA Department
- Establish and maintain a tracking mechanism to monitor daily requirements
- Identify and implement key process improvements to areas to enhance systems, gain site efficiencies and elevate GMP requirements
- Create, review and write procedures
- Review current systems and procedures and implement changes where appropriate to improve productivity
- Provide analytic
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