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Par Formulations Pvt. Ltd.
Par Formulations Pvt. Ltd. is inviting applications from experienced pharmaceutical professionals for multiple Quality Assurance (QA) positions at its Chennai manufacturing facility. This is an excellent opportunity for qualified B.Pharm/ M.Pharm candidates looking to advance their careers in the pharmaceutical industry.
Company
Par Formulations Pvt. Ltd.
Job Location
Chennai, Tamil Nadu
Open Positions
1. Senior Associate – Quality Assurance (IPQA)
Experience Required: 6–10 Years
Qualification: B.Pharm / M.Pharm
Key Responsibilities
- Plan and execute shopfloor IPQA activities, including line clearance, in-process checks, and sampling of intermediates and finished products.
- Perform sampling for hold time studies and maintain retained samples under controlled storage conditions.
- Ensure compliance and calibration of IPQC instruments.
- Acknowledge maintenance requests and conduct impact assessments before closure.
- Perform visual inspection, reserve sample destruction, and maintain the reserve sample room.
- Review batch manufacturing records and investigate deviations or errors.
- Release bulk products and perform QA-related SAP transactions.
- Approve or reject procedures affecting the identity, strength, quality, and purity of drug products.
2. Assistant Manager – Quality Assurance
Experience Required: 8–15 Years
Qualification: B.Pharm / M.Pharm
Key Responsibilities
- Review and approve process validation, exhibit batch, engineering batch, and scale-up protocols and reports.
- Review and approve packing validation protocols and reports.
- Review master and executed batch records.
- Handle New Product Introduction (NPI) activities.
- Review and approve hold time study protocols and reports.
- Review and approve cleaning validation and verification documents.
- Prepare, review, and approve Standard Operating Procedures (SOPs).
- Participate in walkthroughs and self-inspection activities.
- Prepare impact assessment and risk assessment documents.
- Participate in incident investigations, OOT, and Phase II OOS investigations.
- Prepare, review, and approve Annual Product Reviews (APR).
Eligibility
- Qualification: B.Pharm / M.Pharm
- Relevant pharmaceutical manufacturing Quality Assurance experience as specified for the position.
- Strong understanding of GMP, validation, documentation, compliance, and quality systems.
How to Apply
Interested candidates can send their updated CV to:
Email: Nagarajan.patchaiappan@endo.com
WhatsApp: 7010660108
Note: Ensure your resume highlights your Quality Assurance experience, validation activities, documentation expertise, and regulatory compliance knowledge before applying.
Apply as early as possible to increase your chances of being shortlisted.
To apply for this job email your details to Nagarajan.patchaiappan@endo.com.
