ACULIFE Healthcare Private Limited is conducting a walk-in interview for Quality Assurance (QA), Quality Control (QC), and Analytical Development Laboratory (ADL) positions at its sterile/injectable manufacturing plant in Sachana, Ahmedabad district, Gujarat. Candidates with relevant qualifications and experience in pharmaceutical manufacturing, quality control, and analytical development can attend the interview on 30 October 2026.
Job Details
| Particulars | Details |
|---|---|
| Company | ACULIFE Healthcare Private Limited |
| Job Type | Walk-in Interview |
| Departments | Quality Assurance (QA), Quality Control (QC), Analytical Development Lab (ADL) |
| Plant | Sterile / Injectable Plant |
| Qualifications | B.Sc, M.Sc, B.Pharm, M.Pharm |
| Experience | 0–5 years for QA and QC; 2–5 years for ADL |
| Interview Date | 30 October 2026 (Friday) |
| Interview Time | 08:30 AM to 01:00 PM |
| Preferred Candidates | Male candidates preferable |
| Job Location | Sachana, Viramgam, Ahmedabad, Gujarat |
| Application Email | recruitment@aculife.co.in; rajeshthakor@aculife.co.in |
Positions Available at ACULIFE Healthcare
1. Quality Assurance (QA)
Experience: 0–5 years
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
Plant Experience: Sterile / Injectable Plant
Key areas include:
- In-Process Quality Assurance (IPQA)
- Quality Management System (QMS)
- Laboratory QA
- Validation
- QA documentation
- Compliance
- Vendor and audit support
2. Quality Control (QC)
Experience: 0–5 years
Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
Plant Experience: Sterile / Injectable Plant
Key areas include:
- Raw material testing
- In-process testing
- Stability testing
- Finished product testing
- Microbiology
- Instrumental analysis
3. Analytical Development Laboratory (ADL)
Experience: 2–5 years
Qualification: M.Sc. in Analytical Chemistry, B.Pharm, M.Pharm
Plant Experience: Sterile / Injectable Plant
Key areas include:
- Analytical method development
- Method validation
- Method transfer
- Instrument handling and troubleshooting
- Technical support
Roles and Responsibilities
Quality Assurance (QA)
- Perform in-process quality assurance activities in sterile manufacturing.
- Implement and maintain the Quality Management System (QMS).
- Review and approve SOPs, BMRs, BPRs, and other documents.
- Handle batch record reviews and change control management.
- Support process, equipment, and cleaning validation activities.
- Manage deviations, Out of Specification (OOS) investigations, and Corrective and Preventive Actions (CAPA).
- Support regulatory and customer audits, including USFDA and EU audits.
- Ensure GMP compliance and maintain quality standards.
Quality Control (QC)
- Analyse raw materials, packaging materials, in-process samples, and finished sterile products.
- Operate analytical instruments such as HPLC, GC, UV, and dissolution equipment.
- Perform method validation, method transfer, and routine testing.
- Conduct microbial testing and environmental monitoring, where applicable.
- Ensure compliance with pharmacopoeial and regulatory requirements, including IP, USP, and BP.
- Maintain laboratory documentation, data integrity, and compliance.
- Perform stability sample analysis and trend reviews.
Analytical Development Laboratory (ADL)
- Develop and optimise analytical methods for injectable products.
- Develop and validate methods using HPLC, UPLC, GC, UV-Visible, dissolution, and related techniques.
- Perform analytical method transfer and technology transfer to QC.
- Troubleshoot analytical instruments.
- Prepare documentation in accordance with regulatory requirements.
- Conduct stability, forced degradation, and method robustness studies.
- Prepare analytical reports and interpret analytical data.
Eligibility and Qualifications
Candidates should meet the qualification and experience requirements for their preferred department.
| Department | Eligible Qualifications | Experience |
|---|---|---|
| QA | B.Sc, M.Sc, B.Pharm, M.Pharm | 0–5 years |
| QC | B.Sc, M.Sc, B.Pharm, M.Pharm | 0–5 years |
| ADL | M.Sc. Analytical Chemistry, B.Pharm, M.Pharm | 2–5 years |
Experience in a sterile or injectable pharmaceutical manufacturing plant is specified for all three departments.
Required Skills
Based on the listed responsibilities, relevant technical areas include:
- QA: IPQA, QMS, GMP compliance, documentation, validation, deviation management, CAPA, and audit support.
- QC: HPLC, GC, UV, dissolution testing, stability analysis, microbiology, and laboratory documentation.
- ADL: Analytical method development, method validation, method transfer, HPLC, UPLC, GC, UV-Visible analysis, and instrument troubleshooting.
ACULIFE Healthcare Walk-In Interview 2026: Date, Time and Venue
Interview Date: 30 October 2026 (Friday)
Interview Time: 08:30 AM to 01:00 PM
Venue:
ACULIFE Healthcare Private Limited
Near Railway Crossing, Sanand–Viramgam Highway
Village: Sachana, Taluka: Viramgam
District: Ahmedabad – 382150, Gujarat
Application Email Addresses:
