India's DMPLOI - Jobs & Networking AppUnison Pharmaceuticals Pvt. Ltd. has announced a Walk-In Interview for experienced professionals in Quality Control (OSD), Production, Packing, and Engineering departments. Candidates with qualifications ranging from ITI, Diploma, B.Sc, M.Sc, B.Pharm, B.E., and B.Tech are invited to attend the interview at the company’s manufacturing facility in Sanand, Ahmedabad, Gujarat.
This recruitment drive offers excellent career opportunities in the pharmaceutical manufacturing sector for professionals with experience in OSD manufacturing, QC laboratories, packaging operations, and engineering maintenance.
Walk-In Interview Overview
Particulars Details
Company Name
Unison Pharmaceuticals Pvt. Ltd.
Job Type
Walk-In Interview
Interview Date
19th July 2026 (Sunday)
Interview Time
10:00 AM to 3:00 PM
Job Location
Sanand, Ahmedabad, Gujarat
Industry
Pharmaceutical Manufacturing (OSD)
Interview Venue
Unit III – 7, 8, 9 Steel Town, Opp. Nova Petrochemicals,
Village: Moraiya, Taluka: Sanand,
District: Ahmedabad – 382213, Gujarat
Website: www.unisonpharmaceuticals.com
Department-wise Vacancy Details
1. Quality Control (OSD)
Analyst – HPLC
Qualification
B.Pharm
M.Sc
B.Sc
Experience
2–6 Years
Reviewer – Stability, QMS & Raw Material
Qualification
B.Pharm
M.Sc
Experience
5–12 Years
2. Production Department
Supervisor – Coating / Compression / Granulation / Production QMS Specialist
Qualification
B.Pharm
Experience
1–6 Years
Operator – Coating / Compression / Capsule
Qualification
ITI / Diploma
Experience
2–8 Years
3. Packing Department
Supervisor – Primary & Secondary Packing / Packing QMS Specialist
Qualification
B.Pharm / M.Sc
Experience
1–6 Years
Operator – Primary & Secondary Packing
Qualification
ITI / Diploma
Experience
2–8 Years
4. Engineering Department
OSD Plant Maintenance (Technician/Engineer)
Qualification
B.E./B.Tech (Instrumentation, Electrical, Mechanical)
ITI/Diploma (Electrician, Fitter, Instrumentation)
Experience
2–8 Years
Utility Maintenance (Technician/Engineer)
Qualification
B.E./B.Tech (Instrumentation, Electrical, Mechanical)
ITI/Diploma (Electrician, Fitter)
Experience
2–8 Years
Documents Required
Candidates should carry:
Updated Resume/CV
Passport Size Photograph
Salary Proof
Educational Certificates
Experience Certificates
Government Photo ID
Why Join Unison Pharmaceuticals?
Reputed pharmaceutical manufacturing company
Excellent career growth opportunities
Exposure to OSD manufacturing operations
Modern manufacturing facility
Opportunity to work with experienced pharmaceutical professionals
Important Instructions
Reach the venue before the reporting time.
Carry original documents along with photocopies.
Dress in formal interview attire.
Candidates meeting the required qualifications and experience are encouraged to attend.
Technical FAQs
1. What is HPLC and why is it important in pharmaceutical Quality Control?
High Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, quantify, and determine the purity of pharmaceutical products, raw materials, and finished formulations. It ensures products meet regulatory quality standards.
2. What are the responsibilities of a Production QMS Specialist?
A Production QMS Specialist manages documentation, SOP compliance, deviation handling, CAPA implementation, change control, and ensures manufacturing follows GMP and quality management system requirements.
3. What is the difference between Primary and Secondary Packing?
Primary Packing directly contacts the product, such as blister packs and bottles. Secondary Packing includes cartons, labels, shipper boxes, and packaging used for transportation and branding.
4. What skills are required for OSD Plant Maintenance Engineers?
Candidates should have knowledge of preventive maintenance, breakdown troubleshooting, HVAC systems, compressed air, water systems, electrical equipment, instrumentation, PLC basics, and GMP compliance in pharmaceutical plants.
5. What is Stability Testing in pharmaceutical Quality Control?
Stability testing evaluates how a drug product maintains its quality, potency, purity, and safety under various environmental conditions over time. It helps determine product shelf life and storage conditions.
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