OneSource, an initiative by Arcolab, is hosting a walk-in drive for talented professionals to join our state-of-the-art facility in Doddaballapura, Bengaluru (Unit II). We’re hiring Executives, Senior Executives, and Team Leaders across Drug Product (DP) Manufacturing, Drug Substance (DS) Manufacturing, Engineering & Projects, and QA Validation departments. If you have 2-15 years of experience in pharmaceuticals, particularly in sterile injectables or bioprocessing, mark your calendar for Sunday, March 23, 2025, and join us at Stelis Biopharma in Bangalore!
Job Opportunities Overview
Multiple Departments, Diverse Roles
We’re seeking skilled candidates for roles in DP Manufacturing, DS Manufacturing, Engineering & Projects, and QA Validation. This is an exciting opportunity to work with cutting-edge technologies and contribute to a leading CDMO (Contract Development and Manufacturing Organization).
Job Details
Department: DP (Drug Product) Manufacturing
- Designation: Executive | Senior Executive
- Qualification: B.Sc, B.Pharm, M.Sc, M.Pharm
- Experience: 2-8 years in sterile injectables
- Skills Required:
- Operation of isolators and lyophilizers
- Handling equipment for cartridges (B+S), vials, and pre-filled syringes (PFS, B+S)
Department: DS (Drug Substance) Manufacturing
- Designation: Executive | Senior Executive
- Qualification: M.Sc, B.Tech, M.Tech (Biotechnology, Microbiology)
- Experience: 2-8 years
- Skills Required:
- Expertise in upstream and downstream operations (microbial and mammalian processes)
- Proficiency with single-use systems
- Knowledge of cGMP compliance and safety awareness
Department: Engineering & Projects
- Designation: Executive | Senior Executive
- Qualification: Diploma, B.Tech, B.E. (Mechatronics, Instrumentation, Electrical, Mechanical)
- Experience: 2-15 years
- Skills Required:
- Expertise in HVAC systems
- Knowledge of DP and DS process equipment
- Skills in instrumentation and electrical systems
Department: QA Validation
- Designation: Executive | Senior Executive
- Qualification: B.Pharm, M.Pharm
- Experience: 2-8 years
- Skills Required:
- Expertise in qualification and validation activities
- Preparation, execution, and review of qualification/validation documents
- Validating and qualifying GMP equipment
- Work Location for All Roles: Doddaballapura, Bengaluru (OneSource – Unit II)
Walk-In Interview Details
Event Information
Join us for an on-the-spot interview—no pre-registration required!
- Date: Sunday, March 23, 2025
- Time: 9:00 AM – 4:00 PM
- Venue: Stelis Biopharma, #293, Jigani Link Road, Bommasandra, Anekal Taluk, Bangalore – 560105
- HR Contacts:
- Nikhila V: nikhila.v@arcolab.com
- Pooja Thakkar: pooja.thakkar@arcolab.com
How to Apply
Walk-In Process
Attend the interview at the specified venue with your updated resume and relevant documents (e.g., educational certificates, experience letters, ID proof). For more details, visit www.onesourceCDMO.com.
Why Join OneSource?
Innovate with Us
At OneSource, you’ll enjoy:
- Opportunities to work with advanced sterile injectable and bioprocessing technologies
- A collaborative environment focused on cGMP compliance and innovation
- A chance to grow with a leading CDMO in Bengaluru
Quick Reference Table
| Department | Designation | Qualification | Experience | Key Skills |
|---|---|---|---|---|
| DP Manufacturing | Executive | Sr. Executive | B.Sc, B.Pharm, M.Sc, M.Pharm | 2-8 Years |
| DS Manufacturing | Executive | Sr. Executive | M.Sc, B.Tech, M.Tech (Biotech/Micro) | 2-8 Years |
| Engineering & Projects | Executive | Sr. Executive | Diploma, B.Tech, B.E. (Mech/Elec/Instr) | 2-15 Years |
| QA Validation | Executive | Sr. Executive | B.Pharm, M.Pharm | 2-8 Years |
We’re excited to meet you! Bring your expertise to OneSource and help us deliver excellence in pharmaceutical manufacturing. See you on March 23, 2025, at Stelis Biopharma in Bangalore!
