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Levim Lifetech Hiring For Quality Assurance

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Levim Lifetech

Bachelor’s or Master’s in Biotechnology / Biochemistry / Microbiology or related field

Chennai, Tamil Nadu

1 Year

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Levim Lifetech is inviting applications for the position of Quality Assurance (QA) Associate in the biopharmaceutical sector. This is an excellent opportunity for candidates with 1+ year QA experience and strong knowledge of GMP, GLP, and regulatory compliance to advance their careers in the pharma and biotech industry.

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If you’re looking for a Quality Assurance job in biopharma, this role offers exposure to QMS, audits, documentation systems, and regulatory processes, making it ideal for career growth.


📌 Job Details

  • Company: Levim Lifetech
  • Department: Quality Assurance
  • Designation: Associate
  • Experience: Minimum 1 Year
  • Qualification: Bachelor’s or Master’s in Biotechnology / Biochemistry / Microbiology or related field
  • Industry: Biopharmaceutical / Life Sciences

🧪 Key Responsibilities (Quality Assurance Associate)

  • Support QMS activities including deviation, CAPA, OOS, OOT, and incident management
  • Assist in document control (SOPs, logs, master lists) using manual and DMS systems
  • Ensure timely document review, issuance, tracking, and archival
  • Support internal and external audits and follow-up on CAPA actions
  • Assist in validation, calibration, and qualification documentation
  • Prepare monthly QA reports, trend analysis, and management review presentations (MRM)
  • Coordinate with cross-functional teams for compliance and document updates
  • Support vendor qualification and maintain related QA documentation
  • Assist in GMP training programs and QA induction
  • Provide support for regulatory submissions and market complaint investigations
  • Track and ensure timely closure of QMS activities across departments

🎓 Qualifications & Skills Required

  • Bachelor’s or Master’s degree in Biotechnology, Microbiology, Biochemistry, or related field
  • Minimum 1 year of experience in Quality Assurance (QA) in biopharma/pharma industry
  • Strong understanding of GMP, GLP, and regulatory guidelines
  • Knowledge of QMS systems, CAPA, deviations, and audit processes
  • Good documentation, analytical, and communication skills

💼 Benefits of Joining Levim Lifetech

  • Opportunity to work in a growing biopharmaceutical company
  • Hands-on experience in QMS, audits, and regulatory compliance
  • Exposure to documentation systems (DMS) and validation processes
  • Career growth in Quality Assurance and regulatory domains
  • Collaborative and compliance-driven work environment

📩 How to Apply

Interested candidates can apply by sending their updated resume to:

📧 Email: hr@tevim.in

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