Attend the OneSource Specialty Pharma Walk-In Drive on July 6, 2025, in Bengaluru for QC, QA, DP Manufacturing & Microbiology roles. Apply to work in USFDA, EU-GMP certified pharma facilities. Immediate joiners preferred.
🚀 OneSource Specialty Pharma Walk-In Interview – DP Manufacturing, Microbiology, QC & QA Roles | July 6, 2025 | Bengaluru
OneSource Specialty Pharma, formerly known as Stelis Biopharma, invites skilled pharma professionals to a walk-in interview drive for hiring in Drug Product (DP) Manufacturing, Microbiology, Quality Control, and Quality Assurance roles. The event takes place on Sunday, July 6, 2025, in Bengaluru, Karnataka.
As India’s first specialty pharma CDMO, OneSource provides end-to-end solutions in biologics, complex injectables, and drug-device combinations through 5 USFDA, EU-GMP, and ANVISA-approved facilities. We’re backed by over 30 years of CDMO excellence via Arcolab.
📅 Walk-In Interview Details
- Date: Sunday, July 6, 2025
- Time: 9:00 AM to 4:00 PM
- Venue: OneSource Specialty Pharma, Unit 1 (R&D Facility), #293, Jigani Link Road, Bommasandra, Anekal Taluk, Bengaluru, Karnataka – 560105
- Work Location: Unit 2 (DS & DP Manufacturing Facility), Doddaballapura, Bengaluru – 561203
Required Documents:
- Updated resume (2 copies)
- Educational certificates (original + photocopies)
- Last 3 months’ payslips + latest increment letter
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Must have experience in regulated plants (USFDA, EU-GMP, ANVISA)
- Candidates interviewed at OneSource in the last 6 months are ineligible
- Sterile injectable or biopharma experience preferred
- Immediate joiners highly preferred
💼 Open Positions at OneSource Specialty Pharma
1. Drug Product (DP) Manufacturing
- Designation: Executive / Sr. Executive
- Qualification: Diploma / B.Sc / B.Pharm / M.Sc / M.Pharm
- Experience: 2–8 years in sterile injectables
Key Responsibilities:
- Handle washing, tunnel operations, PFS, vials, cartridges
- Perform CIP/SIP, compounding, filtration, autoclave ops
- Operate isolators, lyophilizers, single-use systems
- Maintain cGMP documentation (BMR, SOPs)
Skills:
- Aseptic technique, USFDA/EU-GMP familiarity, sterile practices
2. Microbiology
- Designation: Executive / Sr. Executive
- Qualification: B.Sc / M.Sc (Microbiology or Biotechnology)
- Experience: 2–8 years in sterile injectables
Key Responsibilities:
- Environmental monitoring, MLT, gas testing
- Qualification of lab instruments
- Follow aseptic techniques, SOPs, audit readiness
Skills:
- GLP, aseptic operations, microbial test methods
3. Quality Control (QC)
- Designation: Executive / Sr. Executive / Team Leader
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: 2–12 years
Key Responsibilities:
- Analytical testing using HPLC, GC, UV, TOC, FTIR
- Data management using LIMS
- Method validation, stability, OOS investigations
Skills:
- Proficiency in analytical equipment, cGMP/GLP compliance
4. Quality Assurance (QA – QMS / IPQA)
- Designation: Executive / Sr. Executive
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: 2–8 years
Key Responsibilities:
- IPQA for DS and DP facilities
- Handle CAPA, deviations, QMS processes
- Audit documentation and compliance oversight
Skills:
- Strong QMS & documentation background, regulatory knowledge
✨ Why Work at OneSource Specialty Pharma?
🌍 Global CDMO Leadership
- India’s first specialty pharma CDMO
- 5 facilities approved by USFDA, EU-GMP, ANVISA
- 35 ANDAs filed and 19 US commercial products
⚖️ Regulatory Excellence
- Experience global regulatory compliance firsthand
- Contribute to manufacturing for top pharma innovators
🎓 Innovation Ecosystem
- Work on PFS, autoinjectors, soft gels, and biologics
- Leverage partnerships like Bhami’s HILOPRO® platform
⬆️ Growth & Stability
- 1,200+ employees, 200+ technical experts
- Targeting $400M revenue by FY28–29
- 4.0/5 rating on AmbitionBox for job security
🚪 How to Apply
👉 Walk-In
Attend with documents at OneSource R&D Facility (Unit 1), Bommasandra, Bengaluru on July 6, 2025.
If you can’t attend, email your resume to:
Mention subject line as: “Job Title – Department” (e.g., QC Executive – Injectable) Include:
- Total experience
- Current & expected CTC
- Notice period
📄 About OneSource Specialty Pharma
Previously Stelis Biopharma, OneSource is now a leading CDMO under Arcolab, rebranded in February 2024. Our 5 Bengaluru-based manufacturing units cater to sterile injectables, drug-device combos, and biologics.
📊 Quick Stats:
- HQ: Bengaluru, Karnataka
- Founded: 2007 (as Stelis)
- Market Cap: ₹24,616 crore (as of June 2025)
- Workforce: 1,200+ employees
Visit: www.onesourcecdmo.com
⚠️ Important Disclaimer
OneSource does not charge fees for job applications or interviews. Report scams or unauthorized offers to: cs@onesourcecdmo.com
Join OneSource Specialty Pharma and build your career in a globally recognized, innovation-driven CDMO!
