Umedica Laboratories Pvt. Ltd. has announced a major walk-in interview drive for experienced pharmaceutical professionals across Production, Quality Assurance (QA), Quality Control (QC), Engineering & Maintenance, Packaging Development (PDD), Technology Transfer (TTD), and Oral Liquid Manufacturing departments.
The recruitment drive will be conducted on 26 June 2026 for positions at the company’s globally approved formulation manufacturing plant in Vapi, Gujarat. Candidates with experience in regulated pharmaceutical environments and exposure to USFDA, EU GMP, or TGA-approved facilities are encouraged to attend.
About Umedica Laboratories Pvt. Ltd.
Established in 1982, Umedica Laboratories Pvt. Ltd. is a leading pharmaceutical formulation manufacturer and exporter. The company produces injectables, tablets, capsules, suspensions, dry syrups, and other formulations for global markets including the USA, UK, Canada, Australia, and Europe.
With approvals from USFDA, EU GMP, and TGA Australia, Umedica has built a strong reputation for quality, compliance, and innovation in pharmaceutical manufacturing.
Walk-In Interview Details
| Particulars | Details |
|---|---|
| Company | Umedica Laboratories Pvt. Ltd. |
| Interview Date | 26 June 2026 |
| Time | 09:30 AM to 04:00 PM |
| Venue | Hotel Fressia by Express Inn, Next to Big Bazar, Ostawal Empire, Boisar-Tarapur Road, Boisar – 401501 |
| Job Location | Vapi, Gujarat |
| Industry | Pharmaceutical Formulations |
| Experience Required | 2–10 Years |
| Qualification | ITI, Diploma, B.Pharm, M.Pharm, B.Sc, M.Sc, B.E, B.Tech, M.E |
Available Departments and Positions
1. Tablet Manufacturing
Positions:
- Officer to Assistant Manager
- Technical Associate
Qualification:
- B.Pharm, M.Pharm, M.Sc
- ITI/Diploma
Experience:
- 2–10 Years
Key Responsibilities
- Dispensing, granulation, compression, coating operations
- Online documentation and QMS activities
- Operation of RMG, FBD, FBP, Roll Compactor
- PLC/SCADA-based compression machines
- Capsule filling and coating equipment handling
2. Tablet Packing
Positions:
- Officer/Senior Officer
- Technical Associate
Qualification:
- B.Pharm, M.Pharm, B.Sc, M.Sc
- ITI/Diploma
Experience:
- 2–5 Years
Key Responsibilities
- Blister packing operations
- Cartonator operations
- Track & Trace systems
- BPR documentation
- SOP compliance and manpower management
3. Engineering & Maintenance
Positions:
- Officer/Senior Officer
- Technician
Qualification:
- B.E, B.Tech, M.E
- ITI/Diploma
Experience:
- 2–5 Years
Key Responsibilities
- Plant maintenance
- Utility operations
- HVAC systems
- Fire hydrant systems
- EHS compliance
- QMS activities
4. Quality Control (QC)
Positions:
- Officer / Executive / Deputy Manager
Qualification:
- B.Pharm, M.Pharm, B.Sc, M.Sc
Experience:
- 2–10 Years
Required Skills
- HPLC, GC, Dissolution, UV Spectrophotometer
- LCMS operation
- Method Validation
- Stability Studies
- OOS/OOT Investigation
- Raw Material & Finished Product Analysis
- FTIR, KF, Auto Titrator handling
5. Quality Assurance (QA)
Positions:
- Officer / Senior Officer
Qualification:
- B.Pharm / M.Pharm
Experience:
- 2–5 Years
Required Skills
- IPQA activities
- Line Clearance & Equipment Qualification
- BMR/BPR Review
- APQR Data Management
- Audit Trail Review
- cGMP Compliance Monitoring
- Artwork Approval
- Validation Activities
- Customer Query Handling
6. Packaging Development Department (PDD)
Positions:
- Officer / Senior Officer
Qualification:
- Diploma / B.E in Printing & Packaging
Experience:
- 2–5 Years
Responsibilities
- Artwork development and review
- Packaging design activities
- Regulatory packaging compliance
7. Technology Transfer Department (TTD)
Positions:
- Officer / Executive
Qualification:
- B.Pharm / M.Pharm
Experience:
- 2–5 Years
Responsibilities
- Process transfer planning
- Scale-up activities
- Exhibit and submission batch coordination
- Risk assessment and regulatory compliance
- Product lifecycle management
8. Oral Liquid & Oral Dry Powder Manufacturing
Positions:
- Officer to Senior Officer
- Technical Associate
Qualification:
- B.Pharm, M.Pharm, M.Sc
- ITI/Diploma
Experience:
- 2–7 Years
Responsibilities
- Bulk manufacturing
- Filtration and homogenization
- Filling machine operations
- Bottle labeling
- Induction sealing
- Torqueing and capping
- QMS documentation
Eligibility Criteria
Candidates should possess:
- Pharmaceutical industry experience
- Exposure to regulated manufacturing facilities
- Knowledge of cGMP, SOPs, and documentation practices
- Relevant educational qualifications
- Strong compliance and quality orientation
Note: Only candidates with pharmaceutical industry exposure are eligible.
Documents Required
Candidates attending the walk-in interview should carry:
- Updated Resume
- Passport Size Photograph
- Educational Certificates (Original & Photocopy)
- Last Three Months Bank Statements
- Last Three Months Salary Slips
- Latest CTC Proof
Benefits of Joining Umedica Laboratories
- Opportunity to work in a USFDA, EU GMP & TGA-approved facility
- Exposure to international pharmaceutical markets
- Career growth in regulated manufacturing environments
- Learning opportunities across multiple dosage forms
- Professional development and skill enhancement
How to Apply
Interested candidates can directly attend the walk-in interview on 26 June 2026.
Candidates unable to attend may send their updated CV to:
📧 recruitment.hr@umedicalabs.com
📧 sudhantillu.hr@umedicalabs.com