Ajanta Pharma Limited Hiring for CQA – US FDA Approved Facility
Looking for Quality Assurance jobs in a US FDA approved pharma company?
Ajanta Pharma Limited is inviting applications from suitable candidates for its US FDA approved formulation facility located at Paithan, Dist. Chh. Sambhajinagar, Maharashtra.
Candidates with experience in CQA and QMS activities can apply before the deadline.
Company & Work Location
Company Name: Ajanta Pharma Ltd
Facility: US FDA Approved Formulation Facility
Work Location: B-4/5/6 MIDC Area, Paithan,
Dist.: Chhatrapati Sambhajinagar, Maharashtra – 431148
Job Openings Details
1) Department: CQA
Designation: Officer / Executive Level (as per experience)
Experience: 02 to 05 years
Qualification: B. Pharm / M. Sc.
Work location: Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra
Key skill or Job Description:
Master data creation in LIMS.
GLP-compliance documentation and master document creation in LIMS.
2) Department: CQA
Designation: Senior Level (as per experience)
Experience: 12 to 14 years
Qualification: B. Pharm / M. Pharm
Work location: Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra
Key skill or Job Description:
Experience in multiple formulation domains.
QMS activities- CAPA, deviation, incident etc.
To participate in Self-Inspection.
Harmonization of Quality System.
Prepare & review the standard operating procedure.
Able to deliver training to the sites on QMS elements.
Able to access the CAPA extension of one site to other sites or areas and extend the same.
Important Dates
Suitable candidates can share their application on or before February 28, 2026.
How To Apply
Interested candidates can share their updated resume at:
Email ID: cvptn@ajantapharma.com
Mention “Application for CQA – Paithan” in the subject line of the email.
Who Can Apply
• Candidates with experience in CQA, QMS, GLP documentation and LIMS.
• Professionals from formulation manufacturing units.
• Candidates having exposure to US FDA regulatory standards.
• B.Pharm, M.Sc and M.Pharm qualified professionals as per role requirement.
Career Growth Opportunity
Working at a US FDA approved formulation facility provides strong exposure to global regulatory audits and compliance systems.
CQA professionals can advance into Quality Compliance Head, Site QA Lead or Global QMS roles.
Hands-on experience in LIMS, CAPA management and self-inspection processes significantly enhances long-term career prospects in pharmaceutical quality assurance.
Interview Preparation Tips
• Revise GLP, QMS, CAPA and deviation handling concepts.
• Be ready to explain your experience with LIMS master data and documentation.
• Prepare examples related to audit handling and self-inspection.
• Keep SOP review and quality harmonization experience ready for discussion.
• Carry updated CV with detailed regulatory exposure.
Frequently Asked Questions (FAQ)
1) What is the job location?
Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra.
2) What qualification is required?
B.Pharm, M.Sc or M.Pharm (as per experience level).
3) What is the experience requirement?
2–5 years for junior level and 12–14 years for senior level.
4) What is the last date to apply?
February 28, 2026.
5) How to apply for Ajanta Pharma CQA jobs?
Send your updated resume to cvptn@ajantapharma.com
before the deadline.
If you are searching for Pharma Quality Assurance Jobs in Maharashtra, CQA Jobs in Paithan, LIMS Documentation Jobs or US FDA Pharma Jobs 2026, this is a valuable opportunity to grow your pharmaceutical career.
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| Ajanta Pharma Limited CQA Recruitment 2026 – Paithan, Maharashtra |
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