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Titan Laboratories Walk-In Interview – Pharma Jobs in Production, QA, QC & More on Sunday, 22nd March 2026

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Titan Laboratories Pvt Ltd & Titan Pharmaplus Pvt Ltd are conducting a major walk-in drive for experienced male candidates in pharmaceutical manufacturing. Exciting opportunities await in production jobs, QA jobs, QC jobs, packing, R&D, engineering, and regulatory affairs at their Mahad facility. Attend the walk-in interview on Sunday, 22nd March 2026 in Goa.

About the Company

Titan Laboratories Pvt Ltd and Titan Pharmaplus Pvt Ltd form a leading integrated pharmaceutical group specializing in sustained/modified-release pellets, granules, capsules, formulations, and APIs.

Since its inception, the company has built a strong reputation with WHO-GMP, EU-GMP, and TGA Australia certifications. It ranks among the top pellet formulation manufacturers in India and exports over 98% of its production to more than 30 countries, including the UK, Australia, and various EU markets.

The Mahad MIDC facility focuses on innovation, stringent quality standards, regulatory compliance, and global supply of high-quality pharmaceutical products.

Job Details

  • Company Name: Titan Laboratories Pvt Ltd and Titan Pharmaplus Pvt Ltd
  • Experience Required: Minimum 3 years (varies by role – up to 12+ years for senior positions)
  • Qualification: ITI, B.Sc./M.Sc. (Chemistry), B.Pharm/M.Pharm, D.Pharm, Diploma (Chemical/Electrical/Mechanical/Instrumentation), BE Chemical, MBA (HR/Supply Chain), Any Graduate
  • Location: Mahad, Raigad, Maharashtra (Plot No E 27/1,2,3, Mahad MIDC, Village Jite)
  • Work Type: On-site with rotational shifts mandatory
  • Gender: Male candidates only

Job Description

Titan Laboratories Pvt Ltd large-scale walk-in interview targets experienced professionals across multiple departments in API and Formulation plants. Positions range from operator-level to managerial roles in production, quality, engineering, R&D, warehouse, HR, and regulatory affairs.

Production Department

  • Positions: Manager, Executive, Officers, Operator
  • Key Areas: API planning & execution, troubleshooting, solvent recovery, formulation (FBE, capsule filling, RMG, compression, coating pan, ointment)
  • Experience: Minimum 3 years and above
  • Qualification: ITI, B.Sc./M.Sc., B.Pharm, D.Pharm, Diploma Chemical, BE Chemical

Packing Department

  • Positions: Asst Manager, Executive, Officer, Operator
  • Key Areas: Blister (ELMACH 3010/3000/2500), bottle machine, Discovery Bmax, cartonator
  • Experience: Minimum 4–10 years
  • Qualification: ITI, Diploma, B.Sc./M.Sc., B.Pharm

Quality Assurance (QA)

  • Positions: Executive, Officer
  • Key Areas: IPQA, documentation, QMS, GMP, audit, SOPs, validation, API process
  • Experience: 3–8 years
  • Qualification: B.Sc./M.Sc. (Chemistry), B.Pharm, D.Pharm

QA – FDA Licensing

  • Positions: Asst Manager, Sr Executive, Executive, Officer
  • Key Areas: Test licenses, product manufacturing licenses, NOCs, FDA queries, inspections
  • Experience: Minimum 3 years and above
  • Qualification: B.Sc./M.Sc., B.Pharm, M.Pharm

Quality Control (QC)

  • Positions: Manager, Executive, Officer
  • Key Areas: Chemical & instrumental analysis (HPLC, UV, KF, AAS, auto titration, dissolution), microbiology review
  • Experience: 3–12 years
  • Qualification: B.Sc./M.Sc., B.Pharm, D.Pharm

Microbiology

  • Positions: Sr Executive, Executive
  • Experience: 3–8 years

Engineering Department

  • Positions: Executive, Officer, Fitter, Electrician, Instrumentation
  • Key Areas: Maintenance, instrumentation, utilities, documentation, QMS, change control
  • Experience: 3–8 years (some roles 6–8 years)
  • Qualification: Diploma Electrical/Mechanical/Instrumentation, ITI

Warehouse

  • Positions: Manager, Executive, Officer
  • Key Areas: ERP operation, troubleshooting, permit system, fire fighting, SOP, GMP, audit
  • Experience: 3–12 years
  • Qualification: B.Sc., M.Sc., BE, B.Tech + ADIS (select roles)

R&D – ADL (Formulation)

  • Positions: Executive, Officer
  • Key Areas: Method development, HPLC & dissolution handling, validation review (assay, dissolution, RS)
  • Experience: Minimum 3 years and above
  • Qualification: M.Sc., B.Pharm, M.Pharm

R&D – API & ADL

  • Positions: Executive, Officer
  • Key Areas: API synthesis, intermediates, literature search, scale-up, HPLC/GC method development
  • Experience: 3–10 years
  • Qualification: M.Sc., M.Pharm

HR & Admin

  • Positions: Asst Manager, Sr Executive
  • Key Areas: Core HR, licensing, payroll, recruitment, statutory compliance, audits
  • Experience: Minimum 10 years and above
  • Qualification: MBA HR, PGDM

Regulatory Affairs

  • Positions: Executive, Officer
  • Key Areas: EU guidelines, dossier preparation, customer guidelines & complaints
  • Experience: 3–8 years
  • Qualification: M.Sc., B.Pharm, M.Pharm

Skills & Qualifications Required

  • Hands-on experience in API manufacturing, formulation equipment, and troubleshooting
  • Proficiency in analytical instruments (HPLC, UV, GC, dissolution apparatus, KF, AAS)
  • Strong understanding of GMP, QMS, validation, IPQA, SOP writing, audits
  • Knowledge of regulatory submissions (FDA, EU dossiers), scale-up, method development
  • Warehouse & ERP system operations, supply chain basics
  • Maintenance skills (electrical, mechanical, instrumentation)
  • Willingness to work in rotational shifts

Key Responsibilities

  • Operate and troubleshoot production & packing machinery
  • Perform in-process quality checks and documentation
  • Conduct chemical/instrumental analysis and stability testing
  • Develop and validate analytical methods (assay, dissolution, RS)
  • Prepare regulatory dossiers and handle FDA/EU compliance
  • Manage warehouse dispensing, material indent, and ERP entries
  • Execute preventive maintenance and instrumentation calibration
  • Ensure adherence to GMP, safety, and audit requirements

Benefits & Perks

  • Career progression in a globally exporting pharma company
  • Exposure to advanced GMP-certified manufacturing processes
  • Competitive compensation and performance-based growth
  • Professional learning environment with international standards
  • Long-term job stability in a reputed pharmaceutical group

How to Apply

Email your updated CV along with relevant documents to: recruitments@titanpharmaplus.in

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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Titan LinkedIn page.

Titan Laboratories Walk-In Interview 2026: Pharma Jobs in Production, QA, QC & More

For more pharmaceutical job openings and recruitment alerts across India, visit Pharma Recruiter.

Prepare now and apply confidently!

Walk-in Interview Details

  • Date: Sunday, 22nd March 2026
  • Time: 9:30 AM to 5:00 PM
  • Venue: Hotel The Classic Verna, Plot No U115/A, opposite Siemens, Industrial Estate, Verna 403722, Goa, India
  • Contact Persons: Ashwini Borule, Sagar Malusare, Sandesh Kadam, Pravin Kalambe
  • Phone Numbers: 8655355868 / 7719818726 / 7249398549 / 7249393770

Important Note: This walk-in is exclusively for male candidates. Come in formal dress code and bring: latest salary structure, last 3 months’ salary slips, qualification & experience certificates, bank statement, appointment letter, and increment letter.

Why Join Titan Laboratories?

Titan offers a stable, growth-oriented career in one of India’s leading pellet and formulation manufacturers. Work in a highly compliant, innovative environment with global exposure, continuous learning, and the opportunity to contribute to quality medicines reaching patients worldwide.

Frequently Asked Questions (FAQs)

Who can attend this walk-in interview?

Experienced male candidates with 3+ years in relevant pharmaceutical roles (production, QA, QC, etc.) and matching qualifications.

Are freshers eligible?

Limited opportunities may exist for freshers with relevant degrees (B.Pharm, M.Sc., etc.), but most roles require minimum experience.

What documents are mandatory for the interview?

Latest salary structure, last 3 months’ payslips, qualification certificates, experience letters, bank statement, appointment & increment letters.

Is prior experience in GMP mandatory?

Yes, knowledge of GMP, QMS, audits, and regulatory standards is essential for most technical and quality positions.

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