Senior QC+QA Trainer(Lab Experience Required)

Job Title: Senior QC + QA Trainer (Pharma / Biotech Laboratory)

Location: Remote

Job type: Part-time

Job Summary:

QC + QA Trainer

Key Responsibilities:

Training & Development

• Develop and deliver structured training programs on

  QC laboratory techniques, QA systems, and GMP compliance

  .
• Conduct

  practical laboratory training

  (analytical instruments, wet chemistry, microbiology as applicable).
• Train teams on

  Good Documentation Practices (GDP), Data Integrity (DI), and OOS/OOT handling

  .
• Prepare and update

  SOP-based training modules

  and

  competency assessments

  .
• Conduct

  refresher training, audits-based retraining, and new hire onboarding sessions

  .

Technical & Quality Expertise

• Provide hands-on training in

  HPLC, GC, UV-Vis, FTIR, Dissolution, Wet Chemistry

  , and

  analytical data review

  .
• Guide QA and QC personnel on

  Change Control, Deviation, CAPA, and Internal Audits

  .
• Ensure all training programs align with

  cGMP, GLP, ISO, and regulatory (USFDA, MHRA, WHO) guidelines

  .
• Support QA in

  documentation review, batch record review, and laboratory compliance

  .

Training System Management

• Maintain

  training matrices

  , records, and competency evaluation logs.
• Collaborate with QA Training/HR teams for periodic training plan updates.
• Perform

  gap assessments

  and recommend improvement actions.
• Participate in

  regulatory inspection readiness and training audits

  .

Education:

• M.Sc. / B.Pharm / M.Pharm / B.Sc. in Chemistry, Biochemistry, Microbiology, or related discipline.

Experience:

• Minimum

  10–15 years

  total experience in QC and QA within the

  pharmaceutical/biotech/FMCG

  domain.
• Minimum

  5 years of direct laboratory experience

  (analytical or microbiology lab).
• Prior

  training, mentoring, or internal trainer experience

  is preferred.

Technical Competencies:

• Strong knowledge of

  GMP, GLP, GDP, Data Integrity, QMS

  .
• Expert in

  analytical method validation, calibration, and documentation

  .
• Familiar with

  regulatory inspection observations (FDA, EU, WHO, MHRA)

  .
• Proficient in

  root cause analysis, deviation management, CAPA systems

  .

Soft Skills:

• Excellent communication and presentation skills.
• Strong documentation and report-writing skills.
• Ability to coach and mentor multi-level teams.
• Proactive, detail-oriented, and organized approach to training delivery.