Career Opportunity: Walk-in Interview for OSD Production Professionals
A prominent Contract Development and Manufacturing Organization (CDMO) in India is significantly expanding its operations and actively seeking talented pharmaceutical professionals. This presents an exceptional opportunity to join a company renowned for its world-class manufacturing facilities and unwavering commitment to quality, innovation, and regulatory compliance. The organization is currently recruiting for its state-of-the-art New Oral Solid Dosage (OSD) Manufacturing Project, designated as PCH-3.
Walk-in Interview Details:
Prospective candidates are invited to a walk-in interview on 03 & 04 July 2026. The interviews will take place from 09:45 AM to 04:00 PM daily. The primary focus of this recruitment drive is for the Production Department within the new OSD manufacturing facility.
Job Location:
All available positions are based at the company’s facility in Makhnu Majra, Baddi, Himachal Pradesh.
Open Positions and Key Responsibilities:
The company is looking to fill various crucial roles for both Production Officers and Executives, specifically within OSD manufacturing:
- Production Officer – Granulation: Responsibilities include managing Wet/Dry Granulation, Sifting, Milling, and Drying Operations.
- Production Officer – Compression: This role involves overseeing Tablet Compression Operations and performing In-process Quality Checks.
- Production Officer – Coating: Key tasks include handling Pan Coating Operations and meticulously monitoring In-process Parameters.
- Primary & Secondary Packing Officer: This position focuses on Blister Packing, Cartoning, and managing overall Packing Line Operations.
- Documentation / Batch Record Executive: Duties entail preparing and reviewing Batch Manufacturing Record (BMR/BPR) documentation, ensuring record accuracy, and maintaining compliance.
- QMS Executive – Production (Manufacturing & Packing): This role focuses on implementing and managing Quality Management System (QMS) activities, including CAPA (Corrective and Preventive Actions), Deviations, Change Control, Investigations, and ensuring audit readiness.
Eligibility Criteria:
Applicants must hold a qualification of B.Pharm, M.Pharm, B.Sc, or M.Sc (or an equivalent degree). A minimum of 2 to 5 years of relevant experience in OSD Pharmaceutical Manufacturing is essential. Candidates with demonstrable production experience in regulated pharmaceutical manufacturing environments will be given preference.
Required Skills for Success:
Ideal candidates will possess strong practical knowledge of OSD manufacturing operations, encompassing granulation, compression, coating, and packing processes. Expertise in Batch Manufacturing Record (BMR/BPR) documentation, Quality Management System (QMS) principles, cGMP (current Good Manufacturing Practices), and SOP (Standard Operating Procedure) compliance is critical. Additionally, experience with audit readiness and documentation control will be highly valued.
Documents to Carry:
All attendees must bring the following documents to the interview:
- An up-to-date Resume/CV
- Salary slips from the last three months
- Original and photocopies of Educational Qualification Certificates
- Experience Certificates and any other pertinent supporting documents.
Walk-in Venue:
The interviews will be conducted at the company’s new OSD Project (PCH-3) facility located at:
Makhnu Majra, Baddi, District Solan – 173205, Himachal Pradesh.
Why Consider This Opportunity?
This is an exceptional chance to join India’s leading CDMO pharmaceutical company, offering unparalleled career growth and learning opportunities. Successful candidates will gain valuable exposure to advanced manufacturing technologies, robust quality systems, and the intricacies of regulated pharmaceutical manufacturing practices within a cutting-edge new OSD facility.
