Brooks Steriscience Limited is conducting a walk-in recruitment drive for experienced pharmaceutical professionals across Quality Assurance, Production, Quality Control, Quality Control Microbiology and API Production functions.
The recruitment drive is associated with the company’s dedicated Carbapenem Facility and includes openings ranging from Officer-level positions to senior leadership roles. Candidates with relevant experience in API and pharmaceutical formulation manufacturing, particularly from regulated manufacturing environments, can attend the interview.
The walk-in interview is scheduled for September 27, 2026, in Vapi, Gujarat.
Brooks Steriscience Walk-In Interview 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Brooks Steriscience Limited |
| Facility | Dedicated Carbapenem Facility |
| Departments | QA, Production, QC, QC Microbiology & API Production |
| Job Location | Vapi, Gujarat |
| Walk-In Date | September 27, 2026 |
| Walk-In Time | 10:00 AM – 6:00 PM |
| Interview Mode | Walk-in |
| Experience | 1–20 Years, depending on role |
| Qualifications | Pharmacy, Chemistry, Microbiology, Biotechnology, Engineering & Technical qualifications |
| Venue | Fortune Park Galaxy, Vapi |
| Salary | Not specified |
About Brooks Steriscience Limited
Brooks Steriscience Limited operates pharmaceutical manufacturing facilities, including a dedicated Carbapenem Facility.
The current hiring drive covers multiple technical and quality functions associated with pharmaceutical formulation and API manufacturing. The recruitment notice particularly highlights candidates with experience in regulated manufacturing environments, including USFDA and EU-GMP facilities.
Brooks Steriscience Recruitment 2026 – Job Openings
The company has multiple vacancies across QA, Production, QC, QC Microbiology and API Production.
Quality Assurance – QMS
Position: Executive / Senior Executive
Qualification: M.Pharm / B.Pharm / M.Sc.
Experience: 5–8 years
The role focuses on quality management system activities within pharmaceutical operations.
Quality Assurance – Validation
Position: Officer / Senior Officer
Qualification: M.Pharm / B.Pharm / M.Sc.
Experience: 2–5 years
Relevant experience includes validation activities, equipment qualification and associated documentation.
QA – Lab QC Chemical
Position: Officer / Senior Officer
Qualification: B.Sc. / M.Sc. Chemistry / B.Pharm
Experience: 3–5 years
The role is associated with chemical laboratory quality control activities.
QA – Lab QC Microbiology
Position: Officer / Senior Officer
Qualification: B.Sc. / M.Sc. Chemistry / Microbiology
Experience: 2–5 years
Candidates should have relevant microbiology laboratory experience.
Quality Assurance – IPQA
Position: Officer / Senior Executive
Qualification: M.Pharm / B.Pharm / M.Sc.
Experience: 2–8 years
The role covers in-process quality assurance activities within pharmaceutical manufacturing.
Production – Formulation
Aseptic Area Operations
Position: Operator
Qualification: ITI / Diploma / B.Sc. / B.Pharm
Experience: 3–6 years
Candidates should have relevant exposure to aseptic manufacturing operations.
Lyophilizer Machine Operation
Position: Operator
Qualification: ITI / Diploma / M.Sc. / B.Pharm
Experience: 2–5 years
The position requires experience in operating and handling lyophilizer equipment.
Production Area Supervision
Position: Officer / Senior Officer / Executive
Qualification: B.Pharm / M.Sc.
Experience: 5–7 years
The role involves supervision of pharmaceutical production area activities.
Visual Inspection
Position: Operator
Qualification: ITI / Diploma
Experience: 1–3 years
The position is focused on visual inspection activities within pharmaceutical manufacturing.
Packing
Position: Senior Officer / Executive
Qualification: D.Pharm / B.Pharm / B.Sc. / M.Sc.
Experience: 5–8 years
The role covers pharmaceutical packing operations and related supervision.
Production QMS Supervision
Position: Officer / Senior Officer / Executive
Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
Experience: 3–8 years
Candidates should have relevant experience in quality-system activities associated with production operations.
Quality Control
QC Reviewer
Position: Executive / Senior Executive
Qualification: B.Sc. / M.Sc. Chemistry / Analytical Chemistry / Pharmaceutical Sciences
Experience: 6–8 years
The role involves review-related responsibilities within the Quality Control function.
QC Analyst
Position: Officer
Qualification: B.Sc. / M.Sc. Chemistry / Analytical Chemistry / Pharmaceutical Sciences
Experience: 3–4 years
Candidates should have relevant pharmaceutical analytical laboratory experience.
Quality Control Microbiology
Environmental Monitoring
Position: Officer / Senior Officer / Executive
Qualification: B.Sc. / M.Sc. Microbiology / Biotechnology
Experience: 2–8 years
The position focuses on environmental monitoring and microbiology activities within pharmaceutical manufacturing.
API Production
Sterile & Non-Sterile API
Position: AGM / DGM
Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 15–20 years
This senior-level position requires extensive experience in API manufacturing operations.
Sterile / Non-Sterile Shift In-Charge
Position: Executive / Senior Executive
Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 8–12 years
The role is associated with shift-level supervision of sterile and non-sterile API manufacturing.
Sterile – Filling & Consolidation
Position: Officer / Senior Officer
Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 2–5 years
Candidates should have relevant experience in sterile API filling and consolidation operations.
Non-Sterile Crystallization
Position: Officer / Senior Officer
Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 2–5 years
The position focuses on crystallization activities in non-sterile API manufacturing.
API Documentation
Position: Officer / Senior Officer
Qualification: B.Sc. / M.Sc. Chemistry / B.E. / B.Tech.
Experience: 4–7 years
The role is related to documentation activities within API production operations.
Quality Assurance – API
API IPQA
Position: Officer / Senior Officer / Executive
Qualification: M.Pharm / B.Pharm / M.Sc.
Experience: 2–5 years
The position supports in-process quality assurance activities within API manufacturing operations.
Educational Qualification
The recruitment drive includes candidates with qualifications such as:
- B.Pharm
- M.Pharm
- D.Pharm
- B.Sc.
- M.Sc. Chemistry
- Analytical Chemistry qualifications
- Microbiology
- Biotechnology
- B.E.
- B.Tech.
- ITI
- Diploma
The exact qualification requirement depends on the individual position.
Required Skills and Technical Experience
Depending on the position, candidates should have relevant exposure to:
- Quality Management Systems (QMS)
- Risk assessment
- Deviations
- Change control
- Market complaints
- Validation activities
- Equipment qualification
- Protocol preparation
- Chemical analysis
- Analytical laboratory instruments
- IPQA
- Aseptic area operations
- Lyophilizer operation
- Injectable manufacturing
- Visual inspection
- Packing operations
- Analytical testing
- LIMS
- Calibration and qualification
- Environmental monitoring
- Sterile API manufacturing
- Non-sterile API manufacturing
- API filling and consolidation
- Crystallization
- API documentation
Key Responsibilities
Quality Assurance
Depending on the position, QA professionals may support:
- QMS activities and documentation.
- Deviation and change-control processes.
- Risk assessment activities.
- Validation and equipment qualification.
- IPQA activities.
- Manufacturing process compliance.
- Quality documentation and review.
- Market complaint-related quality activities.
Production
Production professionals may be involved in:
- Aseptic manufacturing operations.
- Lyophilizer operation.
- Injectable production activities.
- Visual inspection.
- Pharmaceutical packing.
- Production area supervision.
- Manufacturing documentation and QMS activities.
Quality Control
QC professionals may support:
- Chemical analytical testing.
- Laboratory operations.
- Analytical data review.
- QC documentation.
- Laboratory instrument-related activities.
- Calibration and qualification requirements.
QC Microbiology
Microbiology professionals may be responsible for:
- Environmental monitoring activities.
- Microbiological quality control.
- Maintaining relevant laboratory documentation.
- Supporting microbiological compliance requirements.
API Production
API production professionals may work on:
- Sterile API manufacturing.
- Non-sterile API manufacturing.
- Filling and consolidation.
- Crystallization operations.
- Shift supervision.
- API manufacturing documentation.
Preferred Candidate Profile
The recruitment drive is intended for experienced professionals with relevant backgrounds in:
- Pharmaceutical manufacturing
- API manufacturing
- Formulation manufacturing
- Quality Assurance
- Quality Control
- QC Microbiology
- Chemistry
- Pharmacy
- Biotechnology
- Engineering
Experience in regulated pharmaceutical manufacturing environments, including USFDA and EU-GMP facilities, is highlighted in the recruitment notice.
Employee Benefits
According to the recruitment information, the company provides the following facilities:
- Free AC bus transportation from Vadodara
- Highly subsidized canteen facility
- Health insurance for employees and family
- Accidental insurance
- Term life insurance
Candidates should confirm the applicable terms and eligibility for these facilities during the recruitment process.
Salary / CTC
A specific salary or CTC has not been disclosed in the available recruitment information.
Candidates can discuss compensation and other employment terms with the recruitment team during the hiring process.
Documents to Carry
Candidates attending the walk-in interview should carry:
- Updated Resume / CV
- Relevant educational documents
- Experience-related documents
- Other supporting documents required for employment verification
Candidates should ensure that their resume clearly reflects their relevant department, manufacturing area, equipment exposure and total experience.
How to Apply
Eligible candidates can attend the Brooks Steriscience walk-in interview on September 27, 2026, at the venue mentioned below.
Candidates can also share their updated CV with the recruitment team before attending.
Email: preeti.yadav@brookssteriscience.com
Contact: 8155009405
Walk-In Interview Details
| Particular | Details |
|---|---|
| Company | Brooks Steriscience Limited |
| Facility | Dedicated Carbapenem Facility |
| Interview Date | September 27, 2026 |
| Interview Time | 10:00 AM – 6:00 PM |
| Venue | Fortune Park Galaxy, NH 48, GIDC I, Vapi – 396195, Gujarat |
| Contact | 8155009405 |
| preeti.yadav@brookssteriscience.com | |
| Interview Type | Walk-in |
Important Details Before Attending
- Multiple departments are hiring under the same recruitment drive.
- Experience requirements range from 1 to 20 years, depending on the position.
- Qualification requirements differ by role.
- Candidates should apply according to their specific functional experience.
- Relevant API or formulation manufacturing experience is important for several positions.
- The interview is scheduled for September 27, 2026, from 10:00 AM to 6:00 PM.
- Candidates should carry an updated CV and relevant documents.
- Salary/CTC has not been specified.
Frequently Asked Questions
1. When is the Brooks Steriscience walk-in interview?
The walk-in interview is scheduled for September 27, 2026.
2. What is the interview timing?
The interview will take place from 10:00 AM to 6:00 PM.
3. Where is the interview venue?
The venue is Fortune Park Galaxy, NH 48, GIDC I, Vapi – 396195, Gujarat.
4. Which departments are hiring?
Openings are available across Quality Assurance, Production, Quality Control, Quality Control Microbiology, API Production and API Quality Assurance.
5. What qualifications are accepted?
Depending on the role, qualifications include B.Pharm, M.Pharm, D.Pharm, B.Sc., M.Sc., ITI, Diploma, B.E. and B.Tech.
6. How much experience is required?
The experience requirement varies by position, from 1 year to 20 years.
7. Are API manufacturing professionals eligible?
Yes. Several positions are specifically related to sterile and non-sterile API production, filling, crystallization, shift supervision and documentation.
8. Are QC Microbiology positions available?
Yes. The recruitment includes Environmental Monitoring positions in QC Microbiology for candidates with 2–8 years of experience.
9. What benefits are mentioned?
The recruitment notice mentions AC bus transportation from Vadodara, subsidized canteen, health insurance for employees and family, accidental insurance and term life insurance.
10. How can candidates apply?
Candidates can attend the walk-in interview directly or share their updated CV with preeti.yadav@brookssteriscience.com. The recruitment contact number is 8155009405.
Important Note
Candidates should verify the latest vacancy status, role-specific eligibility, interview arrangements, compensation and employment conditions with Brooks Steriscience before attending.
Recruitment requirements and vacancy availability may change according to the company’s hiring needs. Candidates should carry accurate documents and should not make any payment to third parties in connection with the recruitment unless officially verified by the employer.