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OneSource Specialty Pharma, India’s first specialty pharma Contract Development and Manufacturing Organization (CDMO), invites talented professionals to join our team at our state-of-the-art facilities in Bengaluru. Formerly Stelis Biopharma, OneSource integrates biologics, complex injectables, and soft gelatin capsules, with 30 years of expertise under the Arcolab umbrella.
Our five USFDA, EU-GMP, and ANVISA-approved facilities in Bengaluru support global clients with end-to-end solutions for drug development and manufacturing. Join us to redefine pharmaceutical innovation at our Doddaballapura, Bengaluru manufacturing site!
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: OneSource Specialty Pharma, Unit 2 (DS & DP Manufacturing Facility), Doddaballapura, Bengaluru, Karnataka – 561203
- Contact: Email resumes to nikhila.v@arcolab.com or manjesh.nayak@arcolab.com
Required Documents:
- Updated resume (2 copies)
- Original and photocopies of educational certificates (Diploma/B.Sc/B.Pharm/M.Sc/M.Pharm)
- Last 3 months’ payslips and latest increment letter
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Candidates must have experience in regulated plants (e.g., USFDA, EU-GMP, ANVISA).
- Candidates interviewed at OneSource in the last 6 months are ineligible.
- Preference for candidates with sterile injectables or biopharma experience.
- Immediate joiners preferred.
Open Positions
Drug Product (DP) Manufacturing
- Designation: Executive / Senior Executive
- Qualification: Diploma / B.Sc / B.Pharm / M.Sc / M.Pharm
- Experience: 2–8 years in sterile injectables
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform washing, tunnel operations, filling, and sealing for liquid vials, prefilled syringes (PFS), and cartridges (B+S).
- Execute CIP/SIP, compounding, filtration, and autoclave operations.
- Operate isolators, lyophilizers, and single-use systems.
- Maintain Batch Manufacturing Records (BMR) and ensure cGMP compliance.
Key Skills:
- Hands-on experience with sterile injectable processes and equipment.
- Knowledge of aseptic practices and regulatory compliance (USFDA, EU-GMP).
Microbiology
- Designation: Executive / Senior Executive
- Qualification: B.Sc / M.Sc in Microbiology or Biotechnology
- Experience: 2–8 years in sterile injectables
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Conduct environmental monitoring, microbial limit testing, and compressed gas testing.
- Perform qualification/requalification of microbiology lab equipment.
- Execute aseptic techniques and maintain documentation per SOPs.
- Support regulatory audits (USFDA, ANVISA).
Key Skills:
- Expertise in microbial monitoring and aseptic techniques.
- Familiarity with GLP and regulatory documentation.
Quality Control (QC)
- Designation: Executive / Senior Executive / Team Leader
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: 2–12 years in sterile injectables or biopharma
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform analytical testing using HPLC, GC, UV, TOC, FTIR, and auto-titrators.
- Utilize LIMS for data management and reporting.
- Conduct method validation, stability studies, and OOS investigations.
- Ensure compliance with GLP and regulatory standards.
Key Skills:
- Proficiency in QC instruments and LIMS.
- Strong knowledge of cGMP and regulatory audits (USFDA, EU-GMP).
Quality Assurance (QMS / IPQA)
- Designation: Executive / Senior Executive
- Qualification: B.Pharm / M.Pharm / M.Sc
- Experience: 2–8 years in sterile injectables or biopharma
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform IPQA for Drug Substance (DS) and Drug Product (DP) manufacturing.
- Manage QMS processes, including deviations, CAPA, and change control.
- Ensure compliance with cGMP, GDP, and aseptic practices.
- Support regulatory audits and documentation reviews.
Key Skills:
- Expertise in QMS, IPQA, and regulatory compliance.
- Strong documentation skills and audit experience.
Why Join OneSource Specialty Pharma?
- Industry Leader: Be part of India’s first specialty pharma CDMO, with 5 globally compliant facilities and a team of 1,200+ professionals, including 200+ techno-commercial experts.
- Regulatory Excellence: Work in USFDA, EU-GMP, and ANVISA-approved plants, with a track record of 35 ANDAs and 19 commercialized products in the US.
- Innovative Environment: Contribute to biologics, drug-device combinations (e.g., PFS, autoinjectors), and complex injectables, backed by strategic partnerships like Bhami’s Research Laboratory for HILOPRO® technology.
- Growth Opportunities: Join a company aiming for $400 million revenue by FY28–29, with a 4.0/5 AmbitionBox rating for job security, though career growth is moderate at 3.5/5.
How to Apply
- Walk-In: Attend the interview on July 6, 2025, at OneSource Unit 1, Jigani Link Road, Bengaluru, with all required documents.
- For Those Unable to Attend: Email your updated CV to nikhila.v@arcolab.com or manjesh.nayak@arcolab.com, mentioning the specific role and department (e.g., “QC Executive”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.
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Note: Candidates with sterile injectable or biopharma experience in regulated plants are preferred. Visit www.onesourcecdmo.com for more details.
About OneSource Specialty Pharma
Incorporated in 2007 as Stelis Biopharma and rebranded in February 2024, OneSource Specialty Pharma is a Bengaluru-based CDMO under the Arcolab umbrella, led by Managing Director Neeraj Sharma. With five state-of-the-art facilities in Bengaluru, we specialize in biologics, sterile injectables, drug-device combinations (e.g., PFS, autoinjectors), and soft gelatin capsules.
Our Unit 2 in Doddaballapura is a flagship site for biologics and complex injectables, recently certified by ANVISA. With a market cap of ₹24,616 crore (June 2025) and a team of 1,200+ professionals, we serve global clients like top biotechs and R&D houses.
Important Disclaimer
OneSource Specialty Pharma does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers to cs@onesourcecdmo.com.
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