Chiron Behring Hiring 25 QA & QC Professionals | Freshers Eligible
- Chiron Behring Hiring 25 QA & QC Professionals | Freshers Eligible | Walk-In 14 Feb 2026
- Company Overview
- Job Role & Responsibilities
- Quality Control – Chemical
- Quality Assurance
- Eligibility & Educational Qualifications
- Required Education (Relevant Courses)
- Experience Criteria
- Walk-In Interview Details
- Documents Required
- Frequently Asked Questions (FAQs)
- 1. How many vacancies are available?
- 2. Are freshers eligible?
- 3. Is prior vaccine industry experience mandatory?
- 4. What qualifications are accepted?
- 5. What analytical instruments are used in QC?
- 6. Is this a shift-based role?
- Recruitment Snapshot
Chiron Behring Hiring 25 QA & QC Professionals | Freshers Eligible | Walk-In 14 Feb 2026
Chiron Behring Vaccines Pvt. Ltd., part of the renowned Bharat Biotech group, is conducting a walk-in interview on 14th February 2026 for 25 vacancies at its vaccine manufacturing facility in Ankleshwar, Gujarat. The hiring drive includes positions in Quality Control – Chemical and Quality Assurance departments. Freshers with 0–3 years of experience are eligible for selected Quality Assurance roles, while experienced professionals can apply for both QC and senior QA positions. This is a strong opportunity for candidates seeking pharmaceutical manufacturing jobs, vaccine industry careers, and GMP-compliant quality roles in a regulated environment.
The walk-in interview will be held between 10:00 AM and 2:00 PM at the company’s Ankleshwar plant. Candidates with M.Sc., B.Sc., B Pharmacy, or M Pharmacy qualifications are encouraged to attend.
Company Overview
Chiron Behring Vaccines Pvt. Ltd. operates under the leadership of Bharat Biotech, one of India’s most respected biotechnology and vaccine development companies. Known for its contribution to global immunization programs and innovative vaccine research, the group has established a strong presence in regulated pharmaceutical markets.
The Ankleshwar facility is dedicated to vaccine manufacturing and sterile injectable production. The plant operates under strict regulatory frameworks, including Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and global data integrity standards. The organization follows validated systems, structured documentation practices, and audit-ready quality processes aligned with national and international pharmaceutical regulations.
Job Role & Responsibilities
Quality Control – Chemical
The Quality Control (QC) Chemical team is responsible for analytical evaluation of raw materials, in-process samples, stability samples, and finished vaccine products. The department ensures product quality, safety, and regulatory compliance through validated laboratory testing.
Key Responsibilities:
- Analysis of raw materials and finished products using validated analytical methods
- Operation of HPLC, GC, UV, IR, and dissolution testing instruments
- Stability sample and validation sample analysis
- Investigation and documentation of OOS (Out of Specification) and OOT (Out of Trend) results
- Ensuring compliance with GMP, GLP, and data integrity standards
- Maintaining laboratory documentation and electronic records
- Supporting internal and external regulatory audits
This role is suitable for professionals looking to strengthen their expertise in pharmaceutical quality control, analytical chemistry, and regulated vaccine production environments.
Experience Required: 2–5 Years
Qualification: M.Sc., B.Sc. (Relevant Life Sciences / Chemistry)
Shifts: Applicable
Quality Assurance
The Quality Assurance (QA) department plays a critical role in ensuring that every vaccine batch meets defined regulatory, quality, and safety standards. QA professionals work closely with production, QC, and regulatory teams to maintain compliance across manufacturing operations.
Key Responsibilities:
- Review of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- Handling deviations, OOS, OOT, and CAPA documentation
- Managing Change Control processes and performing risk assessments
- Conducting line clearance and in-process compliance verification
- Supporting validation, equipment qualification, and audit preparation
- Ensuring GMP documentation accuracy and data integrity compliance
- Coordinating with cross-functional departments to maintain regulatory readiness
Experience Required:
- 0–3 Years (Freshers and early-career professionals)
- 11–16 Years (Senior-level experience)
Preferred Industry Background:
- Sterile manufacturing
- Injectable formulations
- Vaccine production facilities
Qualification:
B Pharmacy, M Pharmacy, B.Sc., M.Sc.
Shifts: Applicable
Eligibility & Educational Qualifications
Candidates must meet the required academic and professional criteria to be considered for these pharmaceutical quality roles.
Required Education (Relevant Courses)
B Pharmacy, M Pharmacy, B.Sc Chemistry, B.Sc Microbiology, B.Sc Biotechnology, B.Sc Biochemistry, M.Sc Chemistry, M.Sc Microbiology, M.Sc Biotechnology, M.Sc Biochemistry
Experience Criteria
- Quality Control: 2–5 years of experience in analytical testing within pharmaceutical or vaccine manufacturing industries
- Quality Assurance: 0–3 years for freshers or 11–16 years for senior professionals
Candidates from sterile, injectable, or vaccine manufacturing facilities will have a competitive advantage due to the compliance-intensive nature of the operations.
Strong knowledge of GMP documentation, regulatory compliance, deviation handling, CAPA management, and pharmaceutical quality systems is essential.
Walk-In Interview Details
Date: 14th February 2026
Time: 10:00 AM to 2:00 PM
Venue:
Chiron Behring Vaccines Pvt. Ltd.
Plot No. 3502, G.I.D.C. Estate
P.B. No. 136
Ankleshwar – 393002
Dist. Bharuch, Gujarat, India
Candidates must complete the online registration process if attending the walk-in interview.
Documents Required
- Updated resume (hard copy)
- Soft copy of resume
- One passport-size photograph
- Aadhaar Card
- PAN Card
Carrying complete documentation ensures faster screening and smooth interview processing.
Frequently Asked Questions (FAQs)
1. How many vacancies are available?
There are 25 openings across Quality Control – Chemical and Quality Assurance departments.
2. Are freshers eligible?
Yes. Freshers with 0–3 years of experience can apply for Quality Assurance roles.
3. Is prior vaccine industry experience mandatory?
It is preferred but not compulsory. Candidates from sterile or injectable manufacturing backgrounds will be prioritized.
4. What qualifications are accepted?
B Pharmacy, M Pharmacy, B.Sc., and M.Sc. in relevant life sciences disciplines such as Chemistry, Microbiology, Biotechnology, and Biochemistry.
5. What analytical instruments are used in QC?
Selected candidates will work with HPLC, GC, UV, IR, and dissolution testing systems.
6. Is this a shift-based role?
Yes. Selected candidates must be open to working in shifts as per manufacturing requirements.
Recruitment Snapshot
| Category | Details |
|---|---|
| Company | Chiron Behring Vaccines Pvt. Ltd. (Bharat Biotech Group) |
| Vacancies | 25 Positions – Quality Control (Chemical), Quality Assurance |
| Required Education | B Pharmacy, M Pharmacy, B.Sc (Chemistry, Microbiology, Biotechnology, Biochemistry), M.Sc (Chemistry, Microbiology, Biotechnology, Biochemistry) |
| Experience | Quality Control: 2–5 Years; Quality Assurance: 0–3 Years & 11–16 Years |
