Micro Labs Limited, a renowned Indian pharmaceutical company known for its sterile manufacturing excellence, is actively recruiting experienced professionals for its Quality Assurance (QA) team at the Bommasandra sterile facility in Bangalore. With a strong focus on regulatory compliance, quality systems, and sterile product validation, these roles offer a chance to contribute to high-quality pharmaceutical production in a leading organization.
If you have a background in B.Pharm or M.Pharm and relevant industry experience, this is an excellent opportunity to advance your career in QA within a dynamic sterile environment.
Available QA Positions at Micro Labs Limited
Micro Labs is filling several key roles in the QA department:
- QA – Documentation (Team Leader/Manager) Education: B.Pharm / M.Pharm Experience: 10–13 years Key responsibilities include handling regulatory, customer, and RA document queries; reviewing and approving MBR/APQR; and proficiency in systems like DMS, Trackwise, SAP, LIMS, and Minitab.
- QA – QMS (Executive / Sr. Executive) Education: B.Pharm / M.Pharm Experience: 3–7 years Focus on independently managing systems related to Deviations, Change Control, CAPA, and Complaints.
- QA – Media Fill / Validation (Asst. Manager) Education: B.Pharm / M.Pharm Experience: 8–10 years Ability to lead and handle media fill study qualification and equipment qualification activities.
- QA – Media Fill / Validation (Executive / Sr. Executive) Education: B.Pharm / M.Pharm Experience: 3–7 years Handling media fill studies and equipment qualification processes.
These positions are based at the company’s sterile facility in Bommasandra Industrial Area, Bangalore – a hub for advanced pharmaceutical manufacturing.
Roles and Responsibilities
Successful candidates will play critical roles in ensuring product quality, compliance with cGMP, and smooth operations in a sterile setup. Common duties across roles include:
- Managing documentation, reviews, and approvals for manufacturing and quality records
- Overseeing Quality Management Systems (QMS) elements like deviation handling, change controls, CAPAs, and customer complaints
- Leading or executing media fill studies, process simulations, and equipment qualifications
- Collaborating with cross-functional teams to resolve regulatory and compliance queries
- Utilizing tools such as Trackwise, SAP, LIMS, Minitab, and DMS for efficient QA operations
Required Qualifications and Skills
- Educational Qualification: B.Pharm or M.Pharm from a recognized institution
- Relevant experience in pharmaceutical QA, preferably in sterile/parenteral manufacturing
- Strong knowledge of regulatory guidelines (USFDA, EU, CDSCO, etc.)
- Proficiency in QA systems and software (Trackwise, SAP, LIMS, etc.)
- Excellent analytical, communication, and leadership skills (especially for senior roles)
- Ability to work independently and handle high-pressure situations in a fast-paced environment
Salary and Benefits
While the exact salary is not disclosed in the announcement, similar QA roles at Micro Labs Limited and comparable pharma companies in Bangalore typically offer competitive packages. Realistic salary ranges (based on experience level):
- 3–7 years: ₹5–10 LPA
- 8–13 years: ₹10–18 LPA or higher for managerial positions
Benefits often include performance bonuses, health insurance, provident fund, leave policies, and professional development opportunities typical in the Indian pharmaceutical sector.
How to Apply
Interested and eligible candidates are invited to share their updated resumes with the HR team at the following email addresses:
Please mention the position applied for in the subject line. Only shortlisted candidates will be contacted.
Don’t miss this chance to join Micro Labs Limited’s sterile facility team in Bangalore. Apply soon!
