Bal Pharma Limited is hiring a QA Executive – Formulation (Tablet & Capsule) for its plant in Bommasandra, Bangalore. The position requires 4–5 years of experience in oral solid dosage (OSD) manufacturing, with mandatory experience in tablet and capsule operations. Candidates should have qualifications in B.Pharm, M.Pharm, or M.Sc and knowledge of quality assurance, pharmaceutical documentation, validation, cGMP compliance, and audit handling.
Job Details
| Particulars | Details |
|---|---|
| Company | Bal Pharma Limited |
| Job Role | QA Executive – Formulation (Tablet & Capsule) |
| Department | Quality Assurance (QA) |
| Job Location | Bommasandra, Bangalore |
| Qualification | B.Pharm / M.Pharm / M.Sc |
| Experience | 4–5 Years |
| Dosage Form | Tablets and Capsules (OSD) |
| Application Email | placement@balpharma.com |
| WhatsApp Contact | Kamal – 9540156568 |
Position
QA Executive – Formulation (Tablet & Capsule)
The role focuses on pharmaceutical quality assurance for oral solid dosage manufacturing, including process quality checks, quality management systems, documentation review, validation, regulatory compliance, and audit handling.
Responsibilities and Major Requirements
1. Oral Solid Dosage (OSD) Experience
- Granulation
- Compression
- Coating
- Capsule filling
- Blister packaging
2. Quality Management System (QMS)
- Deviation management
- Change control
- Corrective and Preventive Actions (CAPA)
- Out-of-Specification (OOS)
- Out-of-Trend (OOT)
- Market complaints
- Quality Risk Management (QRM)
3. Pharmaceutical Documentation
- Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) review
- Standard Operating Procedures (SOPs)
- Validation protocols
- APOR/POR documentation
4. In-Process Quality Assurance (IPQA)
- Line clearance
- In-process checks
- Acceptable Quality Level (AQL)
- Sampling
- Good Documentation Practices (GDP)
5. Validation Activities
- Process validation
- Cleaning validation
- Hold time studies
6. Regulatory Compliance
- Current Good Manufacturing Practices (cGMP)
- USFDA requirements
- EU-GMP requirements
- WHO-GMP requirements
- Data integrity, including ALCOA++
7. Audit Handling
- Internal audits
- Customer audits
- Regulatory audits
Eligibility and Qualifications
Candidates applying for the Bal Pharma QA Executive vacancy should meet the following criteria:
- Educational qualification: B.Pharm, M.Pharm, or M.Sc.
- Work experience: 4–5 years.
- Mandatory experience: Tablet and capsule manufacturing.
- Technical background: Experience in OSD processes, pharmaceutical quality assurance, QMS, documentation, validation, and GMP compliance.
Required Skills
- OSD manufacturing process knowledge
- Quality assurance and IPQA
- Deviation, CAPA, change control, OOS, and OOT management
- BMR/BPR review and SOP documentation
- Process and cleaning validation
- cGMP and regulatory compliance
- Data integrity and GDP
- Internal, customer, and regulatory audit handling
How to Apply for Bal Pharma Recruitment 2026
Eligible candidates can share their CV through the following contact details.
Apply for QA Executive – Formulation
Email Your CV
