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Pharmaceutical Microbiology jobs

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    • This includes but is not limited to the unique requirements required for pharmaceutical GMP compliance.
    • Advanced knowledge of GMP and US FDA regulations for…
    • Experience in pharmaceutical manufacturing is preferred.
    • 1-3 years of experience in cGMP regulated pharmaceutical manufacturing environment.
    • Stay updated on industry trends, regulatory changes, and new technologies in the pharmaceutical field.
    • 2-5 years of relevant experience in in GMP QC laboratory…
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    • Proficiency in pharmaceutical manufacturing, protein purification, centrifugation, tangential flow filtration, and cGMP preferred.
    • Pay rate - $54.52 per hour.
    • Microbiology (biotechnology/pharmaceutical ): 10 years (required).
    • Supported by 5 or more years of microbiology laboratory experience within a biotechnology/…
    • Deep knowledge in pharmaceutical drug development, chemical synthesis and pharmaceutical technology.
    • 10+ years experience in pharmaceutical validation, process…
    • Planifier, organiser et animer les rencontres de l'équipe de sécurité alimentaire;
    • Assurer la mise à jour du plan de sécurité alimentaire (HACCP), lorsque…
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    • 10+ years, direct experience in pharmaceutical/biotechnology manufacturing, and quality environments/organizations.
    • This position may require onsite consultant engagements with in the pharmaceutical industry.
    • This pharmaceutical consultant role focuses on applying your GMP…
    • If you have chemistry education and/or hands-on mass spec experience, our client will train you on software verification to ensure your success :)*.
    • 2-5 or more years of experience in a microbiology laboratory in a pharmaceutical company OR.
    • 4-7 or more years of experience in a microbiology laboratory in a…
    • Support compliance with all applicable regulatory, customer, and certification requirements, including SFCR, NHPR, FDA Food and Dietary Supplement, and GFSI-…
    • At least 1 year of experience in R&D in a pharmaceutical or nutraceutical company.
    • Minimum 1-2 year experience in a laboratory and/or commercial setting—…
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    • Strong background in chemistry, microbiology, biochemistry, and mathematics, supporting analytical and operational tasks.
    • Our Medical Lab Technologists provide accurate and timely interpretive and diagnostic specimen testing and reporting.
    • CMLTO registered and in good standing.
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Job Post Details

QC Lab Manager - Pharmaceuticals - job post

Viva Pharmaceutical Inc.
2.5 out of 5 stars
Richmond, BC
$80,000–$100,000 a year - Permanent, Full-time

Job details

Pay

  • $80,000–$100,000 a year

Job type

  • Permanent
  • Full-time

Location

Richmond, BC

Benefits

Pulled from the full job description

  • Vision care
  • Dental care
  • Extended health care

Full job description

Summary:

The position of QC Lab Manager includes, but is not limited, to leading the QC team to perform routine chemical, physical, and microbiological testing and ensure compliance with all aspects of GMP regulations as required by Health Canada, the US FDA and corporate contractual commitments. This includes but is not limited to the unique requirements required for pharmaceutical GMP compliance.

Responsibilities and Duties

  • Direct and lead the QC team to perform routine chemical, physical, and microbiological testing of pharmaceutical and nutraceutical materials/ingredients, formulations and finished products.
  • 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).
  • As required, provide assistance with internal GMP and third party Audits.
  • Coordinate and perform test method development and test method validation.
  • Review, and when required act as a backup, to approve certificates of analysis, stability summary reports, calibration reports, analytical monographs, master batch records and packaging records in compliance with legal regulatory and customer requirements.
  • As required, develop and update policies and SOPs related to GMP regulations.
  • Provide assistance and technical support for equipment or process optimization, validation, calibration, qualification or certification.
  • Collaborate with other departments to resolve quality-related issues.
  • Lead and train quality control teams.
  • Participate in other tasks that may be assigned by the President & CEO.

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 lab 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

Pay: $80,000.00-$100,000.00 per year

Benefits:

  • Dental care
  • Extended health care
  • Vision care

Application question(s):

  • Can you describe your experience with quality control manager.
  • Describe your experience hosting or participating in regulatory audits (e.g., FDA, Health Canada).
  • Explain your experience with the validation of analytical methods (e.g., HPLC, GC) according to ICH guidelines

Work Location: In person

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