Biological E. Limited (BE), a leading Indian vaccine and pharmaceutical company Celebrating Life Every Day, is hosting a Walk-in Interview on June 22, 2025, in Margao, Goa, for roles at our Specialty Injectables Business in Shamirpet, Hyderabad.
We’re seeking both experienced professionals and fresh diploma holders/graduates to join our USFDA-approved facility in Quality Assurance, Quality Control, Microbiology, and Production Pharma departments.
About Biological E. Limited
Founded in 1953, Biological E. is a Hyderabad-based global leader in vaccines (e.g., DTP, Hepatitis B) and specialty injectables, with a presence in 100+ countries. Our Shamirpet facility is USFDA, WHO-GMP, and EU-GMP certified, employing 2,500+ professionals and generating ₹2,000 crore in revenue (FY25). We focus on innovation, affordability, and quality. Learn more at Biological E. Limited.
Walk-in Interview Details
We’re hiring for our Specialty Injectables Business in Shamirpet, Hyderabad. Below are the event details:
| Event Details | Information |
|---|---|
| Date | June 22, 2025 (Sunday) |
| Time | 9:00 AM to 1:00 PM IST |
| Venue | Hotel Grace Majestic, Beside Mathany Saldanha Administrative Complex, Ambaji Road, Fatorda, Margao, Goa 403602 |
| Job Location | Shamirpet, Hyderabad, Telangana |
| Application Email | Careers@Biologicale.com |
| Note | Candidates interviewed or offered a job by BE in the last 6 months should not apply |
Job Opportunities
Below are the open positions, qualifications, experience, and responsibilities at our Shamirpet, Hyderabad facility, focusing on specialty injectables.
1. Quality Assurance
- Designation: Executive / Senior Executive
- Qualification: B.Pharm / M.Pharm / M.Sc.
- Experience: 3–9 years
- Role: In-Process Quality Assurance (IPQA)
- Responsibilities:
- Conduct IPQA checks during injectable manufacturing (filling, compounding, lyophilization).
- Monitor cGMP compliance and aseptic processes.
- Manage deviations, CAPA, and batch record reviews.
- Support USFDA audits and validation activities.
- Skills:
- Expertise in IPQA, cGMP, and USFDA guidelines.
- Knowledge of QMS tools and audit preparedness.
- Strong documentation and analytical skills.
2. Quality Control
- Designation: Executive
- Qualification: B.Pharm / M.Sc.
- Experience: 3–6 years in injectables
- Role: Raw Material (RM) / Finished Goods (FG) / Stability
- Responsibilities:
- Perform analytical testing of RM, FG, and stability samples using HPLC, GC, UV, and dissolution testers.
- Conduct method validation and stability studies.
- Ensure GLP-compliant documentation for regulatory audits.
- Skills:
- Proficiency in HPLC, GC, and stability analysis.
- Knowledge of cGMP, USFDA, and ICH guidelines.
- Experience with injectable product testing.
3. Microbiology
- Designation: Executive
- Qualification: M.Sc. (Microbiology / Biotechnology)
- Experience: 3–6 years
- Role: Testing / Environmental Monitoring (EM)
- Responsibilities:
- Perform microbial testing (e.g., sterility, BET, MLT) for injectables.
- Conduct environmental monitoring in cleanrooms (air, surface, water).
- Ensure compliance with cGMP, GLP, and USFDA standards.
- Skills:
- Expertise in sterility testing, EM, and microbial limits.
- Familiarity with cleanroom protocols and regulatory audits.
- Strong attention to detail and documentation.
4. Production Pharma
- Designation: Officer / Senior Officer
- Qualification: Diploma / B.Sc.
- Experience: 2–6 years
- Role: Filling / Autoclave / Compounding / Lyophilization
- Responsibilities:
- Operate filling machines, autoclaves, compounding vessels, or lyophilizers.
- Maintain aseptic conditions and batch records.
- Ensure cGMP compliance during production.
- Skills:
- Hands-on experience with injectable manufacturing equipment.
- Knowledge of aseptic techniques and SOPs.
- Ability to work in cleanroom environments.
- Designation: Executive / Senior Executive
- Qualification: M.Pharm / B.Pharm / M.Sc.
- Experience: 2–10 years
- Role: Filling / Autoclave / Compounding / Lyophilization
- Responsibilities:
- Supervise filling, autoclave, compounding, or lyophilization operations.
- Ensure batch compliance with USFDA and cGMP standards.
- Support process optimization and validation activities.
- Skills:
- Leadership in injectable production and process troubleshooting.
- Expertise in cGMP, BMR, and regulatory compliance.
- Strong coordination and problem-solving skills.
Why Join Biological E. Limited?
BE offers a rewarding career in a global pharmaceutical leader. Benefits include:
- Competitive Salary: Executives earn ₹5–12 LPA; Officers ₹3–7 LPA in Hyderabad.
- Global Exposure: Work in a USFDA-approved facility exporting to 100+ countries.
- Career Growth: Training in HPLC, IPQA, microbial testing, and cGMP.
- Supportive Culture: Rated 4.0/5 for job security and 3.7/5 for work-life balance (AmbitionBox).
- Modern Facilities: Shamirpet plant features advanced cleanrooms and lyophilizers.
Why These Roles Matter
These roles drive BE’s production of specialty injectables, ensuring quality and safety for global markets. Your work in IPQA, HPLC analysis, microbial testing, or lyophilization supports life-saving formulations, leveraging Hyderabad’s 2,000+ pharma job ecosystem.
Growth Opportunities
BE invests in training for USFDA compliance, analytical techniques, and aseptic manufacturing. The Shamirpet facility offers exposure to global audits, though employees note shift work and high-pressure timelines (3.7/5 work-life balance).
Work Environment
The Shamirpet facility features GMP-compliant cleanrooms and advanced labs, fostering a collaborative, quality-driven culture. Expect shift-based roles with a 4.0/5 employee rating for job security. Challenges include occasional long hours during audits.
How to Attend
Join us on June 22, 2025, from 9:00 AM to 1:00 PM at Hotel Grace Majestic, Margao, Goa. Bring:
- Updated resume.
- Latest increment letter.
- Payslips for the last 3 months.
- Educational certificates.
- Photo ID (Aadhar/PAN).
If unable to attend, email your CV to Careers@Biologicale.com with the subject line “[Department] – [Designation]” (e.g., “QA – Executive”).
Note: Candidates interviewed or offered a job by BE in the last 6 months should not apply.
Preparation Tips
- QA: Highlight IPQA and cGMP audit experience.
- QC: Detail HPLC/GC and stability testing expertise.
- Microbiology: Emphasize sterility testing or EM skills.
- Production: Showcase filling or lyophilization knowledge.
- Prepare for questions like “How do you ensure cGMP in IPQA?” or “What are key HPLC troubleshooting steps?”
Important Disclaimer
Biological E. Limited maintains a transparent recruitment process. We do not charge fees or use free email services (e.g., Gmail, Yahoo) for job offers. Verify opportunities through Careers@Biologicale.com or BE Careers. Report suspicious activities via the website contact form.
Stay Safe from Fraud
- Confirm offers through official BE channels.
- Avoid sharing personal or financial information with unverified sources.
- Contact HR for clarifications.
Why Shamirpet, Hyderabad?
Shamirpet, Hyderabad, is a biotech hub hosting BE’s USFDA-approved facility. With 2,000+ pharma jobs, excellent connectivity, and proximity to Genome Valley, it’s ideal for injectable manufacturing careers.
Join BE’s Mission
Biological E. Limited is Celebrating Life Every Day through innovative injectables and vaccines. By joining our Shamirpet team, you’ll ensure quality for global patients. Attend our walk-in interview on June 22, 2025, in Goa or apply online to join our 2,500+ strong team!
Next Steps
Arrive early for registration on June 22, 2025. The selection process may include technical interviews (e.g., HPLC analysis, aseptic techniques) and document verification. Selected candidates will receive spot offers or follow-up communication.
Contact Us
For queries, email Careers@Biologicale.com or visit BE Contact. Stay updated via BE Careers.
Innovate with BE
Join Biological E. Limited to advance specialty injectables manufacturing. Attend our Walk-in Interview on June 22, 2025, in Margao, Goa, and contribute to global healthcare!
