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Sterilization technician • montreal qc
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Gestionnaire, Validation / Manager, Validation
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Groupe RobertBoucherville, Canada- St. John's, NL (from $ 52,795 to $ 60,415 year)
- Vancouver, BC (from $ 59,606 to $ 60,415 year)
- Mississauga, ON (from $ 50,700 to $ 60,412 year)
- Markham, ON (from $ 40,950 to $ 58,220 year)
- East York, ON (from $ 40,950 to $ 58,189 year)
- North York, ON (from $ 40,950 to $ 58,189 year)
- Edmonton, AB (from $ 43,753 to $ 53,168 year)
- Old toronto, ON (from $ 40,170 to $ 50,700 year)
- Toronto, ON (from $ 40,170 to $ 50,700 year)
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Gestionnaire, Validation / Manager, Validation
Jubilant Pharma, LLCMontreal, Montreal (administrative region), Canada- Full-time
Validation Manager
Jubilant HollisterStier, a subsidiary of Jubilant Pharma Holdings Inc., is currently recruiting for a Validation Manager to join our team!
What do we offer?
A culture that values growth and professional development opportunities, a highly competitive base salary, comprehensive medical, dental, and disability insurance programs, a collective retirement savings plan, and health and wellness programs. Jubilant HollisterStier is a rapidly growing company with offices in Kirkland, Quebec, and Spokane, Washington. A fully integrated contract manufacturing organization, Jubilant HollisterStier has the capability to manufacture sterile injectable preparations, as well as solid and semi-solid dosage forms. Our four facilities in North America and India provide specialized manufacturing services for the pharmaceutical and biopharmaceutical sectors. Jubilant HollisterStier is a proud member of the Jubilant Pharma family. For more information, visit www.jublhs.com.
We will continue, with the utmost care for the environment and society, to enhance value for our customers and stakeholders by delivering innovative products and economically effective solutions through growth, profitability, and judicious investment of resources. If you are ready for a rewarding challenge, we invite you to take the first step and apply today!
Position Objective
Directs the design, planning and execution of the site validation master plan. Ensures that validation activities are in compliance with regulatory agencies, GMP's and guidance documents.
Key Accountabilities
- Directs the designing, planning and execution of the site validation master plan.
- Develops the validation protocols and validation reports for the plant computerized and non-computerized equipment / systems / utilities and automated systems, sterilization / depyrogenation / drying / fill volume processes, inspection validation processes, packaging validation processes, room qualification process and cleaning validation process.
- Establishes qualification requirements and acceptance criteria from the review of Engineering P&ID's drawings, functional specifications, turnover packages, results from Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT) and commissioning and qualification activities.
- Directs the coordination of resources needed to complete validation tests.
- Prepares presentations for regulatory agencies regarding the validation program.
- Provides technical expertise and supports Quality Assurance during regulatory inspections.
- Develops and leads training programs for the validation department.
- Develops, implements and maintains the SOP's for validation department to include the implementation of the validation program and the execution of the qualification tests.
- Ensures compliance of the validation program with the current GMP requirements of the regulatory agencies in the certification program.
- Ensures compliance of the validation program with the current CCS (Contamination Control Strategy) requirements of the site.
- Develops, implements and monitors the site validation procedures in compliance with the Life Cycle approach, ensuring continuous compliance with GMP.
- Coordinates and supervises the activities of validation contractors.
- Reviews, analyzes and evaluates the qualification test results, determines the acceptability, and ensures that test exceptions and protocol discrepancies are properly documented and justified. Reviews and approves IQ, OQ, PQ, CV and PV documents and any other related documents (eg : change controls, SOP, commissioning documents, risk assessments).
- Manages the department budget.
- Supervises a team of Validation Specialists. Responsible for training, performance and evaluations.
- Performs additional duties as assigned by Management.
Key Interfaces
External
External relationship of different service providers and suppliers.
Internal
Education Qualification :
Minimum education : Bachelor’s Degree, preferably in Science / Engineering.
Experience in effectively managing large, complex, cross departmental projects.
Skills Required :
Physical
No special physical demands are required to perform the work.
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