Quality Assurance Jobs at Shalina Healthcare | Chemistry Grads Apply
Are you looking for Quality Assurance Jobs in the pharmaceutical industry that offer hands-on exposure, regulatory learning, and career growth? This exciting opportunity for an Officer – Quality Assurance in Pune is ideal for professionals seeking MSc Chemistry Jobs or Chemistry Jobs with strong involvement in IPQA activities, GMP compliance, and manufacturing quality systems.
About Shalina Healthcare
The organization is a reputed pharmaceutical manufacturing setup committed to delivering high-quality, safe, and compliant products. With a strong focus on GMP, regulatory excellence, and continuous improvement, the company provides excellent career opportunities for professionals seeking stable and growth-oriented Chemistry Jobs and Quality Assurance Jobs in India’s thriving pharma industry.
- Location: Pune, Maharashtra, India
- Experience: 2 – 5 Years
- Job Type: Full Time
Job Description:
What do you become a part of:
The IPQA Officer/Executive will be responsible for ensuring in-process quality assurance activities across all manufacturing operations. The role involves monitoring compliance with SOPs, GMP standards, and regulatory requirements, as well as reviewing documentation and supporting process validation.
What to expect:
- Monitor raw material dispensing activity.
- Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations.
- Conduct validation sampling in accordance with approved validation protocols.
- Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance.
- Perform ERP-related transactions of IPQA.
- Check BSR (Batch Summary Record) and Shipper inspection as per SOP.
- Manage issuance, review, and reconciliation of formats across all departments.
- Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance.
- Ensure cleaning, sanitation, and hygiene in all departments to maintain GMP compliance at all times.
- Perform sampling of In-process, Semi-Finished Goods (SFG), and Finished Goods (FG) as per procedure.
Key Skills & Competencies:
- Strong knowledge of IPQA processes, cGMP, and regulatory guidelines.
- Attention to detail with strong documentation and review skills.
- Proficiency in ERP systems (preferably SAP or equivalent).
- Good communication and coordination skills to work with cross-functional teams.
- Ability to conduct inspections, identify deviations, and drive compliance.
Qualifications & Experience:
- B.Pharm / M.Pharm / M.Sc. in a relevant discipline.
- 2–5 years of experience in IPQA or Quality Assurance within the pharmaceutical industry.
