Freshers Pharma, QA, QC, Production professionals | Aculife Healthcare
- Aculife Healthcare Walk-in Interview – Pharma QA QC Production Sachana
- Company Overview
- Job Role & Responsibilities
- Production Department
- Quality Assurance (QA)
- Quality Control (QC)
- Analytical Development Laboratory (ADL)
- Research & Development and Specialized Roles
- Eligibility / Qualifications
- Location & Salary
- Walk-in Interview Details
- Application Process
- Why Join Aculife Healthcare
- Frequently Asked Questions (FAQs)
- Who can attend this walk-in interview?
- Is this interview open for freshers?
- What type of products does Aculife manufacture?
- Is prior sterile manufacturing experience mandatory?
- How can I apply if I cannot attend the walk-in?
- SEO Title Suggestions
- Job Summary Table
Aculife Healthcare Walk-in Interview – Pharma QA QC Production Sachana
Aculife Healthcare Private Ltd hiring Pharma, QA, QC, Production professionals in Sachana, Ahmedabad. Walk-in interview on 30 Jan 2026.
Aculife Healthcare Private Limited, a well-established pharmaceutical manufacturing company under the reputed Nirma Group, is conducting a walk-in interview for its manufacturing facility at Sachana, Ahmedabad. This hiring drive is focused on strengthening core functions such as Production, Quality Assurance, Quality Control, Analytical Development Laboratory, and Research & Development for sterile and non-sterile formulations. Freshers and experienced professionals with relevant science and pharmacy backgrounds are encouraged to attend.
The company is actively looking for motivated candidates who want long-term careers in regulated pharmaceutical manufacturing environments. This opportunity is ideal for candidates seeking pharma jobs in Ahmedabad, sterile manufacturing careers, QA QC roles in formulation plants, and analytical scientist positions in India.
Company Overview
Aculife Healthcare Private Limited, formerly known as Nirlife, is a flagship pharmaceutical company of the Nirma Group. The organization has built strong credibility in the global pharmaceutical industry through its focus on injectable, sterile, and formulation-based products. Its manufacturing facilities follow international regulatory standards including cGMP, ICH guidelines, and global compliance norms.
Aculife plays a critical role in advancing healthcare by delivering high-quality, affordable pharmaceutical products across domestic and international markets. Working at Aculife offers exposure to regulated manufacturing systems, advanced sterile technologies such as BFS, and robust quality management practices. This makes the company a preferred employer for professionals aiming to grow in pharmaceutical production, quality systems, and analytical research.
Job Role & Responsibilities
Production Department
Candidates in Production will be involved in end-to-end manufacturing operations of parenteral dosage forms including vials, ampoules, bags, and bottles manufactured through BFS technology.
Key responsibilities include:
- Handling sterile manufacturing operations in formulation plants
- Production and packing compliance activities
- Documentation related to batch manufacturing records
- Managing deviations, CCN, CAPA, and investigations
- Supporting remediation and audit readiness activities
- Coordinating with QA and QC teams to ensure product quality
Quality Assurance (QA)
The QA team ensures compliance with regulatory requirements across sterile and non-sterile dosage forms.
Responsibilities include:
- Validation activities and IPQA operations
- Quality Management System documentation
- Compliance handling during audits and inspections
- Review of batch records and SOPs
- Deviation management and change control
- Data integrity and regulatory documentation
Quality Control (QC)
QC professionals support analytical testing and release of pharmaceutical products.
Responsibilities include:
- Chemical and instrumental analysis
- Microbiology testing for sterile products
- Handling laboratory instruments and documentation
- Stability studies and analytical reporting
- Compliance with GLP and GMP requirements
Analytical Development Laboratory (ADL)
ADL roles focus on method development and validation for sterile dosage forms.
Responsibilities include:
- Hands-on operation of HPLC, GC, UV, Dissolution, TOC
- Sterility testing and analytical validation
- Development and transfer of analytical methods
- Compliance with ICH and regulatory standards
- Supporting regulatory submissions
Research & Development and Specialized Roles
Additional openings include:
- Analytical Scientists – Sterile Dosage Forms
- Research Associates – Method Development & Validation
- Quality Control Analysts
- Stability Analysts
- Microbiology Analysts
- Documentation & Compliance Executives
Eligibility / Qualifications
Candidates must hold a science or pharmacy qualification relevant to pharmaceutical manufacturing and quality functions.
Required education includes:
B.Sc, M.Sc, B.Pharm, M.Pharm, Pharmaceutical Sciences, Chemistry, Microbiology, Biochemistry, Biotechnology, Analytical Chemistry, Life Sciences
Experience criteria:
- Production: 0 to 6 years in parenteral manufacturing
- QA: 0 to 5 years in formulation QA roles
- QC: 0 to 6 years in analytical or microbiology labs
- ADL: 1 to 5 years in analytical method development
Freshers with strong academic knowledge and a willingness to work in regulated pharma environments are also encouraged to attend.
Location & Salary
Job Location:
Aculife Healthcare Private Limited
Near Railway Crossing, Sanand–Viramgam Highway
Village: Sachana, Taluka: Viramgam
District: Ahmedabad – 382150, Gujarat
Walk-in Interview Details
Interview Date: 30 January 2026 (Friday)
Interview Time: 08:00 AM to 11:00 AM
Interview Venue:
Aculife Healthcare Private Limited (Formerly Nirlife)
Near Railway Crossing, Sanand–Viramgam Highway
Village: Sachana, Taluka: Viramgam
District: Ahmedabad – 382150
Candidates are advised to carry updated resumes, educational certificates, experience letters, and recent passport-size photographs.
Application Process
Interested candidates can directly attend the walk-in interview or apply via email.
Email IDs for Application:
recruitment@aculife.co.in
rajeshthakor@aculife.co.in
Mention the department and position applied for in the email subject line for faster processing.
Why Join Aculife Healthcare
- Part of the reputed Nirma Group
- Exposure to sterile and injectable manufacturing
- Strong regulatory and compliance culture
- Career growth in QA, QC, Production, and R&D
- Stable organization with long-term vision
- Learning-driven work environment
Frequently Asked Questions (FAQs)
Who can attend this walk-in interview?
Science and pharmacy graduates including freshers and experienced professionals with relevant backgrounds can attend.
Is this interview open for freshers?
Yes. Freshers with B.Sc, M.Sc, B.Pharm, or M.Pharm qualifications are eligible for trainee roles.
What type of products does Aculife manufacture?
Aculife primarily focuses on sterile injectable formulations, parenterals, and regulated dosage forms.
Is prior sterile manufacturing experience mandatory?
Experience is preferred for experienced roles, but freshers can apply for trainee and junior positions.
How can I apply if I cannot attend the walk-in?
Candidates can send their resumes to the provided email IDs for consideration.
SEO Title Suggestions
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Job Summary Table
| Company | Aculife Healthcare Private Limited |
|---|---|
| Vacancies | Production Trainee, QA Executive, QC Analyst, Analytical Scientist, Research Associate, Documentation & Compliance Executive |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Pharmaceutical Sciences, Chemistry, Microbiology, Biotechnology |
| Experience | 0 to 6 Years depending on role |
To apply for this job email your details to recruitment@aculife.co.in
