India's DMPLOI - Jobs & Networking AppAkums Drugs & Pharmaceuticals Ltd., one of India’s leading CDMO (Contract Development and Manufacturing Organization) pharmaceutical companies, has announced a Walk-In Interview for experienced professionals in the Production Department for its New OSD Manufacturing Project (PCH-3) at Makhnu Majra, Baddi, Himachal Pradesh. This recruitment drive is an excellent opportunity for candidates with experience in OSD pharmaceutical manufacturing to join a fast-growing pharmaceutical organization.
Job Overview
Company: Akums Drugs & Pharmaceuticals Ltd.
Department: Production – New OSD Manufacturing Project (PCH-3)
Job Location: Makhnu Majra, Baddi (H.P.)
Walk-In Dates: 03rd & 04th July 2026
Reporting Time: 09:45 AM to 04:00 PM
Available Positions
Akums is hiring for multiple openings in the following production roles:
Production Officer – Granulation
Production Officer – Compression
Production Officer – Coating
Primary & Secondary Packing Officer
Documentation / Batch Record Executive
QMS Executive – Production (Manufacturing & Packing)
Key Responsibilities
Production Officer – Granulation
Perform wet and dry granulation processes.
Handle sifting, milling, and drying operations.
Follow GMP and SOP requirements.
Production Officer – Compression
Operate tablet compression machines.
Perform in-process quality checks.
Monitor tablet weight, hardness, thickness, and friability.
Production Officer – Coating
Handle pan coating operations.
Monitor coating process parameters.
Ensure uniform coating quality.
Primary & Secondary Packing Officer
Perform primary and secondary packaging activities.
Ensure proper labeling, coding, and packing.
Maintain packaging documentation.
Documentation / Batch Record Executive
Prepare, review, and archive BMRs and BPRs.
Maintain ALCOA+ compliant documentation.
Ensure documentation accuracy and completeness.
QMS Executive – Production
Manage deviations, CAPA, and Change Control.
Maintain training records.
Support internal and external audits.
Ensure GMP compliance across production operations.
Eligibility Criteria
Educational Qualification
Candidates having any of the following qualifications can apply:
B.Pharm
M.Pharm
B.Sc.
M.Sc.
Equivalent Qualification
Experience
2–5 years of experience in OSD Pharmaceutical Manufacturing.
Documents Required
Candidates should carry the following documents during the interview:
Updated Resume / CV
Last 3 Months’ Salary Slips
Educational Qualification Certificates
Experience Certificates (if available)
Unable to Attend?
Candidates who cannot attend the walk-in interview may send their CV via:
Email: recruit.pch3@akums.in
WhatsApp: 8350835062 / 8272052884
Interview Venue
Akums Drugs & Pharmaceuticals Ltd.
New OSD Project (PCH-3)
Makhnu Majra, Baddi,
District Solan, Himachal Pradesh – 173205
Official Website: www.akums.in
Why Join Akums?
India’s leading CDMO pharmaceutical company
Modern OSD manufacturing facility
Career growth opportunities
Exposure to GMP-compliant manufacturing systems
Professional work environment
Multiple production openings
Technical FAQs
1. What is OSD manufacturing in the pharmaceutical industry?
OSD (Oral Solid Dosage) manufacturing involves the production of tablets, capsules, and other solid oral medicines through processes such as dispensing, granulation, compression, coating, and packaging under GMP guidelines.
2. What is ALCOA+ documentation?
ALCOA+ is a data integrity principle that stands for Attributable, Legible, Contemporaneous, Original, Accurate, along with Complete, Consistent, Enduring, and Available. It ensures reliable pharmaceutical documentation.
3. What are the critical in-process checks during tablet compression?
Common in-process checks include tablet weight variation, hardness, thickness, friability, disintegration time, and appearance to ensure product quality and regulatory compliance.
4. What is the purpose of CAPA in pharmaceutical manufacturing?
CAPA (Corrective and Preventive Action) helps identify the root cause of deviations or quality issues, implement corrective actions, prevent recurrence, and improve overall quality systems.
5. What GMP practices should production professionals follow?
Production personnel should strictly follow Standard Operating Procedures (SOPs), Good Documentation Practices (GDP), hygiene requirements, line clearance procedures, equipment cleaning, calibration schedules, and quality control standards to ensure product safety and regulatory compliance.
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