Head of Quality Control – Biotech

Full time @Dei Biopharma posted 1 week ago in HealthCare
  • Post Date : May 9, 2025
  • Apply Before : May 13, 2025
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Job Detail

  • Job ID 26999
  • Career Level  Officer
  • Experience  3 Years
  • Gender  Both
  • Industry  Healthcare
  • Qualifications  Degree Bachelor
  • Job Type  Full time

Job Description

Summary:
DEI BioPharma Ltd., a state-of-the-art Drugs and Vaccines Manufacturing company has successfully completed the first phase of its development project. This phase includes fully equipped facilities for Oral Solid Dosage (OSD) manufacturing, Neutraceuticals, Medical Devices, and mRNA Vaccine production. As we now transition into the operational phase, we are seeking suitable and qualified candidates to help operationalize these newly established facilities. QA Inspectors will be responsible for on-line quality checks and compliance monitoring throughout manufacturing and packaging processes. DEI BioPharma Ltd. is seeking a results-oriented Head of Quality Control (Biotech) to lead all analytical operations related to biologics. The role requires deep scientific expertise and strong leadership to oversee QC testing, data integrity, and compliance for biotech products across the product lifecycle.

Key Duties and Responsibilities:

  1. Lead QC laboratories across microbiology, molecular biology analytical chemistry, and bioassays.
  2. Oversee raw material, in-process and finished product testing for biologics and vaccines.
  3. Ensure robust and compliant method development, validation and technology transfer.
  4. Manage stability studies and environmental monitoring in compliance with ICH and cGMP.
  5. Enforce data integrity principles and ensure readiness for regulatory inspections.
  6. Mentor and grow a high-performing analytical team with specialized expertise.
  7. Drive continuous improvement in lab performance, throughput and compliance.

Qualifications and Experience:

  • PhD in Analytical Chemistry, Biotechnology, or Life Sciences (Master’s with 15+ years of experience may be considered).
  • Minimum of 12 years’ experience in biotech QC, with 5+ years in a senior leadership role.
  • Advanced understanding of biologics manufacturing, immunoassays, and aseptic controls.
  • Direct experience with regulatory inspections and method life cycle management.

How to Apply:

  1. All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Human Resources Manager)
  2. All Application documents should be merged as one document in PDF or .DOC / .DOCX, which should not exceed 10MB
  3. Applications should be sent by email to recruitment@deibiopharma.com with the JOB TITLE IN THE SUBJECT LINE.
  4. Should you not hear from us within twenty-one (21) days from the closing date of this advertisement, you may consider your application to be unsuccessful.

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