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Analyste support testing F/H
3 months ago
Title:
Analyst, Quality Control Development
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 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 developmentEmployee training and organizational development programs, internal mobility programs, and employee recognition programs
The main responsibility for this position is to perform method development, validation and transfer activities to support Quality Control and Operations (Development).
Develop and validate methods within the QC lab for HPLC and other instrumental techniques with the goal of updating and improving existing methods.
IV Drug release testing for product comparison.Perform process validation and cleaning validation testing.
Participate on projects in the area of focus related to process improvement.
Collaborate with other departments to proactively build quality into the processes and systems.
Create and revise QC procedures as required.
Provide support for internal and Regulatory Inspections.
Identify and implement key process improvements to enhance systems, gain site efficiencies and elevate GMP requirements.
Generate, gather and analyze data for reporting purposes.
Complete all training assignments and maintain personal training records.
Initiate, and follow through with actions required to close Change Controls.
Participate in Internal, Customer and Regulatory Audits.
Complete all training assignment and maintain personal training records.
Flexibility to work shift schedules when required
Bachelor's Degree in Chemistry, or related discipline
3-5 years' experience in the pharmaceutical industry in a Quality Control Laboratory.
Knowledge of Pharmaceutical Manufacturing and Packaging an asset
Demonstrated technical writing skills
Knowledge of applicable software including LIMS, Empower and MS Office
Excellent written communication and report writing skills
Advanced ability in investigative techniques to troubleshoot analytical problems
Any deviations to procedures or systems are brought to the Management's attention with logic, data and corrective measures
Ability to support work in other shifts
Working in general office and laboratory environments
Office Based
Taro Pharmaceuticals Inc. embraces diversity in the workplace and is committed to achieving employment equity.
We ensure that our recruitment practices are supportive of this commitment and do not infringe on any characteristics protected by law.
In accordance with the Accessibility for Ontarians with Disabilities Act, 2005, and the Ontario Human Rights Code, Taro Pharmaceuticals Inc.
will provide accommodation throughout the recruitment and selection process to applicants with disabilities.