Quality Manager, Sterile Manufacturing
2 weeks ago
**Summary of Duties**
- Oversees and directs all aspects of the Company’s quality control and quality assurance processes and implements changes as required ensuring compliance with GMP and all relevant regulatory requirements.
- Trains and ensures that all staff members are familiar with SOPs pertaining to their own duties. Hire, supervise and train or oversee training of employees in the use of equipment, instruments, techniques
- Continually monitors facility, materials and processes to ensure compliance with Standard Operating Procedures and regulatory requirements as they pertain to GMP standards.
- Coordinate and oversee all aspects of quality control and quality assurance efforts; Plan, organise and evaluate related daily operations.
- Provides support, recommendations and reports to the President and CEO on all matters pertaining to Quality and Regulatory compliance and requirements
- Oversees and ensures that adequate technology, including security, of electronic storage, data processing, and communication are maintained. Acts as resource to resolve electronic data transmission, storage and retrieval issues.
- Prepare/ oversee quality reports such as, SOP’s, OS, NCR, PD.
- Promote and motivate team and maintain a quality culture.
- Develop equipment and instrument maintenance schedules.
- Maintain inventory of laboratory reagents.
**Required Education/Experience**:
- A Canadian university degree or a degree recognized as equivalent by a Canadian university or Canadian accreditation body in Chemistry or Biochemistry.
- At least five (5) years of practical experience in Quality Control or Quality Assurance in a drug manufacturing.
- Must be able to communicate in English (written and oral).
- Ability to plan, organise and control several tasks and projects concurrently.
- Full cycle implementation skills, (conceptualise, plan, train, implement, validate, etc.).
- Strong analytical skills.
- Must be able to communicate with a wide range of personnel in the hierarchy of customer and regulatory organisations.
**Job Types**: Full-time, Permanent
Pay: $90,000.00 per year
**Benefits**:
- Casual dress
- Company events
- Dental care
- Disability insurance
- Extended health care
- Life insurance
- On-site parking
- Vision care
Schedule:
- Monday to Friday
**Education**:
- Bachelor's Degree (required)
**Experience**:
- Quality Control/Assurance: 2 years (required)
- sterile pharmaceutical manufacturing: 1 year (required)
**Language**:
- English (required)
Work Location: In person
Application deadline: 2022-02-25
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