Qc Laboratory Supervisor

2 weeks ago

Richmond, Canada Viva Pharmaceutical Inc. Full time

**Summary**:
The position of QC Laboratory Supervisor includes, but is not limited to, performing routine chemical and physical testing of pharmaceutical and nutraceutical formulations in support of corporate development projects and/or production support, ensuring all analytical results and documentation are of high quality, generated in a timely fashion, and complying with all aspects of GMP - as required by the Canadian Food and Drugs Act and supporting regulations. This includes but is not limited to the unique requirements required for pharmaceutical GMP compliance

**Responsibilities and Duties**
- Perform routine chemical and physical testing of pharmaceutical and nutraceutical formulations.
- Ensure all analytical results and documentation are of high quality along with data integrity traceability requirements.
- Perform testing in accordance with assigned protocols, methods, or procedures.
- Review and prepare routine technical documents as directed by the QC Manager.
- Direct and lead the QC team as supervisor to perform routine chemical, physical, and microbiological testing of pharmaceutical and nutraceutical materials/ingredients, formulations and finished products.
- Supervise laboratory technicians on how to proceed with analytical tests.
- Ensure all analytical results and documentations are generated of high quality in a timely fashion along with data integrity traceability requirements.
- Participate in Analytical Investigations of out-of-specification, examine results, change control requests when necessary, generate deviation reports, root cause determination, and provide recommendation for corrective actions.
- Ensuring corporate compliance with GMP regulations as required by Health Canada, the US FDA or other jurisdiction with a focus in maintaining the corporate GMP Establishment License (or other legal licenses).
- Coordinate and perform **test method development and test method validation**.
- Provide assistance and technical support for equipment or process optimization, validation, calibration, qualification or certification.
- Demonstrated time management and project organizational skills.

**Qualifications and Skills**
- A Canadian (or assessed as equivalent) B.Sc. degree in an applicable discipline of science (chemistry, biochemistry, biology or related) or specific medical training (pharmacology, pharmacokinetics, nutritional research or related).
- Five or more years of QC management experience in the pharmaceutical, nutraceutical or related industry.
- Advanced knowledge of GMP and US FDA regulations for manufacturing pharmaceutical or nutraceutical products.
- Familiarity with laboratory equipment (e.g. HPLC, GC, and ICP).
- Proven ability to supervise personnel and excellent verbal/written communication skills.

**Job Types**: Full-time, Permanent

**Salary**: From $45,000.00 per year

**Benefits**:

- Dental care
- Extended health care
- Vision care

Schedule:

- 8 hour shift

Application question(s):

- Are you familiar with HPLC?

**Education**:

- Bachelor's Degree (preferred)

**Experience**:

- quality control: 5 years (preferred)
- GMP & USA FDA practical: 1 year (preferred)

Work Location: In person

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