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UMEDICA Laboratories Walk-In Interview for QA, QC, Production, Engineering & Packaging Roles | Apply Now on 26 June 2026

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Looking for pharma jobs in India? UMEDICA Laboratories is conducting a walk-in interview for QA jobs, QC jobs, production jobs, engineering, packaging, and technology transfer roles at its globally approved manufacturing facilities.

About the Company

UMEDICA Laboratories Pvt. Ltd. is a renowned pharmaceutical manufacturing and export company established in 1982. The company specializes in the production of pharmaceutical formulations including injectables, tablets, capsules, suspensions, oral liquids, and dry syrups.

Over the years, UMEDICA has built a strong reputation for delivering high-quality healthcare products that comply with stringent international regulatory standards. The company operates facilities approved by major regulatory authorities including USFDA, EU GMP, and TGA Australia.

With a significant presence across the USA, UK, Canada, Australia, Europe, and several other international markets, UMEDICA continues to expand its global footprint while maintaining a strong commitment to quality, innovation, compliance, and patient safety.

Job Details

  • Company Name: UMEDICA Laboratories Pvt. Ltd.
  • Experience: 2–10 Years (varies by role)
  • Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc, B.E, M.E, B.Tech, Diploma, ITI, Printing & Packaging Diploma
  • Location: Vapi, Gujarat
  • Work Type: On-site
  • Industry: Pharmaceutical Manufacturing
  • Regulatory Exposure: USFDA, EU GMP, TGA Australia Approved Facility

Job Description

UMEDICA Laboratories is hiring experienced pharmaceutical professionals across multiple departments including Manufacturing, Packing, Quality Control, Quality Assurance, Engineering, Packaging Development, Technology Transfer, and Oral Liquid Production.

Candidates with pharmaceutical industry exposure and regulatory manufacturing experience are encouraged to attend the walk-in interview.

Officer to Assistant Manager – Tablet Manufacturing

  • Department: Tablet Manufacturing
  • Market: Regulated Markets (USFDA, EU GMP, TGA)
  • Role: Manufacturing Operations
  • Experience: 2–10 Years
  • Education/Qualification: B.Pharm, M.Pharm, M.Sc

Technical Associate – Tablet Manufacturing

  • Department: Tablet Manufacturing
  • Market: Regulated Markets
  • Role: Equipment Operations
  • Experience: 2–5 Years
  • Education/Qualification: ITI, Diploma

Officer/Senior Officer – Tablet Packing

  • Department: Tablet Packing
  • Market: Regulated Markets
  • Role: Packaging Operations
  • Experience: 2–5 Years
  • Education/Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc

Technical Associate – Tablet Packing

  • Department: Tablet Packing
  • Market: Regulated Markets
  • Role: Machine Operations
  • Experience: 2–5 Years
  • Education/Qualification: ITI, Diploma

Technician – Engineering & Maintenance

  • Department: Engineering & Maintenance
  • Market: Regulated Markets
  • Role: Plant Maintenance and Utilities
  • Experience: 2–5 Years
  • Education/Qualification: ITI, Diploma

Officer/Senior Officer – Engineering & Maintenance

  • Department: Engineering & Maintenance
  • Market: Regulated Markets
  • Role: HVAC, Utility and Maintenance Operations
  • Experience: 2–5 Years
  • Education/Qualification: B.E, M.E, B.Tech

Officer/Executive/Deputy Manager – Quality Control (QC)

  • Department: Quality Control
  • Market: Regulated Markets
  • Role: Analytical Testing and Validation
  • Experience: 2–10 Years
  • Education/Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc

Officer/Senior Officer – Quality Assurance (QA)

  • Department: Quality Assurance
  • Market: Regulated Markets
  • Role: IPQA and Compliance
  • Experience: 2–5 Years
  • Education/Qualification: B.Pharm, M.Pharm

Officer/Senior Officer – Packaging Development Department (PDD)

  • Department: Packaging Development
  • Market: Regulated Markets
  • Role: Artwork and Product Design
  • Experience: 2–5 Years
  • Education/Qualification: Diploma, B.E (Printing & Packaging)

Officer/Executive – Technology Transfer Department (TTD)

  • Department: Technology Transfer
  • Market: Regulated Markets
  • Role: Process Transfer and Scale-Up
  • Experience: 2–5 Years
  • Education/Qualification: B.Pharm, M.Pharm

Officer to Senior Officer – Oral Liquid & Oral Dry Powder

  • Department: Oral Liquid & Oral Dry Powder
  • Market: Regulated Markets
  • Role: Manufacturing Operations
  • Experience: 2–7 Years
  • Education/Qualification: B.Pharm, M.Pharm, M.Sc

Technical Associate – Oral Liquid & Oral Dry Powder

  • Department: Oral Liquid & Oral Dry Powder
  • Market: Regulated Markets
  • Role: Equipment Operations
  • Experience: 2–5 Years
  • Education/Qualification: ITI, Diploma

Skills/Qualifications

  • Knowledge of dispensing, granulation, compression, coating
  • Experience with tablet packing operations
  • Understanding of cGMP requirements
  • Expertise in QMS documentation
  • HPLC, GC, UV, FTIR and LCMS operation
  • Method validation and stability studies
  • OOS and OOT investigation handling
  • Equipment qualification and line clearance
  • Audit trail review and compliance monitoring
  • Technology transfer and process scale-up
  • HVAC, utility and plant maintenance knowledge
  • Artwork review and packaging development
  • Strong communication and teamwork skills
  • Regulatory compliance awareness

Key Responsibilities

  • Execute manufacturing and packaging activities
  • Maintain batch documentation accuracy
  • Perform analytical testing activities
  • Conduct in-process quality checks
  • Monitor GMP compliance requirements
  • Review BMR and BPR documents
  • Handle equipment operations efficiently
  • Support validation activities
  • Perform technology transfer tasks
  • Ensure adherence to SOP requirements
  • Maintain quality and safety standards
  • Support continuous process improvement

Benefits/Perks

  • Opportunity to work in regulated facilities
  • Exposure to international pharmaceutical markets
  • Strong career growth opportunities
  • Learning and development programs
  • Competitive compensation packages
  • Advanced manufacturing technologies
  • Professional work environment
  • Long-term career stability
  • Global regulatory exposure
  • Collaborative workplace culture

How to Apply

Interested candidates can attend the walk-in interview with all required documents.

Candidates unable to attend can send their updated resume to:

UMEDICA Laboratories Walk-In Interview for QA, QC, Production, Engineering & Packaging Roles | Apply Now on 26 June 2026

For more pharmaceutical job updates, interview alerts, and career opportunities, visit Pharma Recruiter: Pharma Recruiter

Apply now and take the next step in your pharmaceutical career with UMEDICA Laboratories.

Walk-in Interview Details

Documents Required

  • Updated Resume
  • Passport Size Photograph
  • Degree Certificates (Original and Photocopy)
  • Last Three Months Bank Statement
  • Last Three Months Pay Slips
  • Latest CTC Proof (Original and Photocopy)

Note: Only candidates with pharmaceutical industry exposure are eligible.

Why You Should Join UMEDICA Laboratories

UMEDICA Laboratories offers professionals an opportunity to build rewarding careers within a globally recognized pharmaceutical organization.

Employees gain valuable exposure to USFDA, EU GMP, and TGA-regulated manufacturing environments while working with advanced technologies and experienced industry professionals.

FAQs

Who can apply for these positions?

Candidates with relevant pharmaceutical industry experience ranging from 2 to 10 years and qualifications specified for individual roles can apply.

Is this a walk-in interview or online interview?

This is a walk-in interview. Candidates can attend directly at the specified venue on the scheduled date.

Can candidates apply through email?

Yes. Candidates unable to attend the interview can send their resumes to the official recruitment email addresses provided above.

What are the career growth opportunities at UMEDICA?

UMEDICA offers growth through regulated market exposure, skill development, leadership opportunities, and international-quality manufacturing operations.

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