OneSource Specialty Pharma has announced a Walk-in Drive for experienced professionals in DP Manufacturing, Engineering & Projects, and Quality Control. This recruitment drive offers an excellent opportunity for candidates with experience in sterile injectable manufacturing, engineering maintenance, and pharmaceutical quality control to join a leading specialty pharmaceutical CDMO.

If you have relevant qualifications and industry experience, attend the walk-in interview on the scheduled date with your updated resume and required documents.

OneSource Specialty Pharma Walk-in Drive– Overview

Particular Details

Company Name

OneSource Specialty Pharma

Job Type

Walk-in Interview

Job Location

Doddaballapura, Bengaluru, Karnataka

Interview Location

Global R&D Facility, #293 Jigani Link Road, Bommasandra, Anekal Taluk, Bengaluru – 560105

Interview Date

26th July 2026 (Sunday)

Interview Time

9:30 AM to 4:00 PM

Designation

Executive / Sr. Executive

Experience

2–10 Years (Department-wise)

Industry

Pharmaceutical CDMO

Departments Hiring

DP Manufacturing

Engineering & Projects

Quality Control

Educational Qualification

DP Manufacturing

B.Sc

B.Pharm

M.Sc

M.Pharm

Engineering & Projects

Diploma

B.Tech

B.E.

Mechatronics

Instrumentation

Electrical

Mechanical Engineering

Quality Control

B.Sc

M.Sc

B.Pharm

M.Pharm

Experience Required

DP Manufacturing

2 to 10 Years

Engineering & Projects

2 to 10 Years

Quality Control

2 to 6 Years

Job Responsibilities

DP Manufacturing

Selected candidates will be responsible for:

Operating isolators and associated equipment.

Handling cartridge filling, vial filling and pre-filled syringe manufacturing.

Operating CIP/SIP skid systems.

Vessel operation and compounding.

Filtration and autoclave operations.

Filter integrity testing.

Exposure to isolator lyophilizer and single-use systems.

Working in sterile injectable manufacturing environments.

Following USFDA and GMP guidelines.

Supporting regulatory inspections and audits.

Engineering & Projects

Responsibilities include:

Preventive and breakdown maintenance of production equipment.

Maintenance of filling lines, vial washing machines and autoclaves.

Maintenance of filtration vessels and packaging equipment.

Utility maintenance including HVAC, Water Systems, Boilers, Chillers and Cooling Towers.

Maintenance of Air Compressors and DG systems.

Troubleshooting PLC, HMI and SCADA systems.

Supporting uninterrupted pharmaceutical manufacturing operations.

Quality Control

Responsibilities include:

Analysis of raw materials and packing materials.

In-process sample testing.

Instrument qualification.

Preparation of SOPs, Specifications and STPs.

Method transfer and validation.

Vendor sample analysis.

Laboratory consumable management.

Maintaining GMP documentation.

Compliance with Health & Safety guidelines.

Skills Required

Manufacturing

Sterile Injectable Manufacturing

Isolator Operation

CIP/SIP

Aseptic Processing

Lyophilization

Autoclave Operation

GMP Compliance

USFDA Audit Exposure

Engineering

Equipment Maintenance

HVAC

Water System

Utility Maintenance

PLC

HMI

SCADA

Instrumentation

Mechanical Maintenance

Quality Control

Raw Material Analysis

Method Validation

Instrument Qualification

Documentation

SOP Preparation

GMP Compliance

Laboratory Testing

Walk-in Interview Details

Interview Date

26th July 2026 (Sunday)

Interview Time

9:30 AM – 4:00 PM

Interview Venue OneSource Specialty Pharma

Global R&D Facility

#293 Jigani Link Road

Bommasandra, Anekal Taluk

Bengaluru – 560105

Work Location OneSource Specialty Pharma

Unit 2 (DS & DP Manufacturing Facility)

Doddaballapura, Bengaluru – 561203

Documents Required

Candidates should carry:

Updated Resume

Recent Passport-size Photographs

Educational Certificates

Experience Certificates

Salary Slips

Latest Increment Letter

Government Photo ID Proof

Why Join OneSource Specialty Pharma?

Leading pharmaceutical CDMO.

Exposure to advanced sterile injectable manufacturing.

Work in USFDA-compliant facilities.

Modern engineering and automation systems.

Excellent career growth opportunities.

Professional work environment.

How to Apply?

Interested and eligible candidates can directly attend the walk-in interview at the specified venue on 26th July 2026 between 9:30 AM and 4:00 PM with all required documents.

For queries, candidates may contact the Human Capital Team through the email addresses mentioned in the official notification.

Technical FAQs

1. What is DP Manufacturing in pharmaceutical industries?

DP (Drug Product) Manufacturing involves converting drug substances into finished dosage forms such as sterile injectables, vials, cartridges, and pre-filled syringes under aseptic conditions following GMP guidelines.

2. What is the purpose of CIP and SIP systems?

CIP (Clean-In-Place) automatically cleans manufacturing equipment, while SIP (Sterilize-In-Place) sterilizes equipment using steam before production, ensuring contamination-free pharmaceutical manufacturing.

3. Why are PLC, HMI, and SCADA systems important in pharmaceutical plants?

These automation systems monitor, control, and record manufacturing operations, improving process reliability, product quality, regulatory compliance, and operational efficiency.

4. What is method validation in Quality Control?

Method validation confirms that an analytical method consistently delivers accurate, precise, specific, and reliable results according to ICH and regulatory guidelines before routine use.

5. Why is GMP compliance essential in sterile manufacturing?

Good Manufacturing Practices (GMP) ensure medicines are consistently produced and controlled according to quality standards, minimizing contamination risks and ensuring patient safety.