Software design supervisor
2 weeks ago
Title:
Supervisor, Quality Control Development
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.
Our reward packages have been designed to meet the needs of our diverse workforce and their families.
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.
Our reward packages have been designed to meet the needs of our diverse workforce and their families. Opportunities for career growth and developmentBenefit 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
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.
Supervise, lead and mentor staff including ongoing coaching, performance feedback and reviews, routine meetings, standard hours, collaboratively identifying objectives and career developmentPlan, 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
Provide troubleshooting of test method and equipment issues.
Identify and implement key process improvements to areas to enhance systems, gain site efficiencies and elevate GMP requirements
Participate in Internal, Customer and Regulatory Audits
Partner with Warehouse and Purchasing to proactively build quality into the processes and systems
Perform monthly Health and Safety Audits and safety awareness training
Other responsibilities and special projects as required
Proficiency with applicable software (LIMs and Empower)
Ability to implement short range strategies and objectives towards enhancing the quality standards of the department
Any deviations to procedures or systems are brought to the Director's attention with logic, data and corrective measures
Implement short range strategies and objectives towards enhancing the quality standards of the department and facility
Bachelor's Degree in Science or related field
strong supervisory experience is an asset
Taro Pharmaceuticals embraces diversity in the workplace and is committed to achieving employment equity.
In accordance with the Accessibility for Ontarians with Disabilities Act, 2005, and the Ontario Human Rights Code, Taro Pharmaceuticals will provide accommodation throughout the recruitment and selection process to applicants with disabilities.
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