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FDC Limited Hiring for Quality Control, Quality Assurance, and Production Roles in Chhatrapati Sambhajinagar

Join FDC Limited, a leading pharmaceutical company since 1936, headquartered in Mumbai, India. Specializing in Ophthalmics, Oral Liquids, Oral Powders, and Topical Powders, FDC operates dedicated facilities approved by USFDA, UK MHRA, WHO-GMP, and PICS.

Our Ophthalmics section features three state-of-the-art Blow-Fill-Seal (BFS) machines, catering to regulated (US, Europe) and semi-regulated (South America, Asia-Pacific, Africa) markets. We’re hiring for Quality Control (QC), Quality Assurance (QA), and Production roles at our advanced manufacturing plant in Chhatrapati Sambhajinagar, Maharashtra, to support our global export operations.

Job Opportunities at FDC Limited

We’re seeking professionals with 3-12 years of experience and freshers with relevant skills for roles in QC, QA, and Production (BFS and Formulation). Positions are based at our USFDA-approved facility in Chhatrapati Sambhajinagar, a key hub for Ophthalmic manufacturing.

Job Location

  • FDC Limited, B-8, MIDC Industrial Area, Waluj, Chhatrapati Sambhajinagar, Maharashtra – 431136

1. Quality Control (QC)

  • Positions:
    • Officer / Senior Officer
    • Executive / Senior Executive
  • Qualification:
    • M.Sc. (Analytical Chemistry, Chemistry)
  • Experience & Skills:
    • Officer/Sr. Officer: 3-6 years in raw material and finished product analysis. Proficient in HPLC, GC, UV-Vis, and LIMS.
    • Executive/Sr. Executive: 6-12 years in analytical method validation, SOPs, change control, and investigations. Strong expertise in HPLC and LIMS.
  • Key Responsibilities:
    • Conduct raw material and finished product testing (Ophthalmics, Oral Liquids) using HPLC, GC, and UV-Vis
    • Perform method validation and transfer per ICH Q2(R1)
    • Manage OOS/OOT investigations and implement CAPA
    • Maintain LIMS data and ensure GLP compliance
    • Support stability studies and regulatory submissions
  • Openings: Multiple (likely 4-6 based on role diversity)

2. Quality Assurance (QA)

  • Position: Senior Officer to Senior Executive
  • Qualification: B.Pharm, M.Pharm
  • Experience: 6-12 years in sterile plant qualification, validation, QMS, and regulatory audits
  • Key Responsibilities:
    • Oversee sterile plant (BFS) qualification and validation
    • Manage QMS activities: deviations, CAPA, change controls
    • Ensure compliance with USFDA, UK MHRA, and WHO-GMP standards
    • Prepare and review SOPs, BMRs, and BPRs
    • Lead regulatory audit readiness and responses
  • Key Skills:
    • Expertise in sterile manufacturing and cGMP
    • Knowledge of QMS and audit preparation
    • Strong documentation and communication skills
  • Openings: Multiple (likely 2-4 based on senior roles)
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3. Production – Blow-Fill-Seal (BFS)

  • Positions:
    • Officer to Senior Executive (Electrical)
    • Trainee Supervisor to Senior Supervisor (Electrical)
    • Officer to Senior Executive (Pharmacy)
  • Qualification:
    • B.E./B.Tech (Electrical) for Officer/Sr. Executive
    • ITI/Diploma (Electrical) for Trainee/Sr. Supervisor
    • B.Pharm/M.Pharm for Officer/Sr. Executive
  • Experience & Skills:
    • Officer/Sr. Executive (Electrical): 3-8 years in BFS operations, sterile area maintenance, troubleshooting, and record-keeping
    • Trainee/Sr. Supervisor (Electrical): 0-5 years in BFS machine handling, pre/post-fill activities, cleaning, and validation
    • Officer/Sr. Executive (Pharmacy): 3-8 years in Ophthalmic batch manufacturing, aseptic processing, and audit readiness
  • Key Responsibilities:
    • Operate and maintain BFS machines for Ophthalmic production
    • Perform aseptic processing, filtration, and sterilization
    • Conduct equipment cleaning, validation, and documentation (BMR/BPR)
    • Troubleshoot electrical and mechanical issues in sterile areas
    • Ensure compliance with USFDA and UK MHRA standards
  • Openings: Multiple (likely 6-10 based on BFS specialization)

4. Production – Formulation

  • Position: Supervisor to Senior Supervisor
  • Qualification: D.Pharm, B.Sc.
  • Experience: 2-8 years in batch manufacturing, filtration, autoclave, sanitization, and documentation (BMR, BPR)
  • Key Responsibilities:
    • Manufacture Oral Liquids, Oral Powders, and Topical Powders
    • Perform filtration, autoclave operations, and sanitization
    • Complete BMRs and BPRs per cGMP standards
    • Support in-process checks and batch release
    • Ensure facility readiness for regulatory audits
  • Key Skills:
    • Knowledge of formulation manufacturing and cGMP
    • Proficiency in BMR/BPR documentation
    • Attention to detail for sanitization and quality
  • Openings: Multiple (likely 3-5 based on formulation scope)

Qualifications and Experience

DepartmentPositionQualificationExperienceKey Skills
Quality ControlOfficer/Sr. OfficerM.Sc. Analytical Chemistry3-6 yearsHPLC, GC, UV, LIMS
Quality ControlExecutive/Sr. ExecutiveM.Sc. Chemistry/Analytical6-12 yearsMethod Validation, HPLC, LIMS
Quality AssuranceSr. Officer to Sr. ExecutiveB.Pharm/M.Pharm6-12 yearsSterile Validation, QMS, Audits
Production (BFS)Officer to Sr. ExecutiveB.E./B.Tech Electrical3-8 yearsBFS Ops, Maintenance
Production (BFS)Tr. Supervisor to Sr. SupervisorITI/Diploma Electrical0-5 yearsBFS Handling, Validation
Production (BFS)Officer to Sr. ExecutiveB.Pharm/M.Pharm3-8 yearsAseptic Processing, Audits
Production (Formulation)Supervisor to Sr. SupervisorD.Pharm/B.Sc.2-8 yearsBatch Mfg, Documentation

Why Join FDC Limited?

FDC Limited, with a legacy since 1936, employs 6,000+ professionals and exports to 50+ countries. Our Chhatrapati Sambhajinagar facility, rated 3.8/5 on AmbitionBox for job security, features dedicated Ophthalmic BFS lines and formulation units, producing 30+ products like Lumefantrine suspensions. Approved by USFDA and UK MHRA, we ensure zero-defect manufacturing. Employees praise the learning environment but note challenges like a 6-day workweek.

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Key Benefits

  • Work in a USFDA-approved, BFS-equipped facility
  • Support global markets with Ophthalmics and formulations
  • Gain experience with advanced tools like HPLC and LIMS
  • Join a 88-year legacy in India’s pharma hub
  • Access opportunities for regulatory audit exposure

How to Apply

Email your CV to roshan.bhurawane@fdcindia.com with subject “Application for [Position] – Chhatrapati Sambhajinagar”. Include:

  • Educational certificates
  • Experience letters and last 3 months’ payslips
  • Aadhar and PAN cards
  • CTC and notice period Prepare to discuss HPLC, QMS, BFS operations, or audit experiences. FDC Limited does not charge recruitment fees; verify communications via @fdcindia.com emails. Immediate joiners preferred.
FDC Limited Hiring for Quality Control, Quality Assurance, and Production Roles in Chhatrapati Sambhajinagar

About FDC Limited

FDC Limited is a pioneer in pharmaceutical manufacturing, operating 10 facilities across India. Our Chhatrapati Sambhajinagar plant specializes in Ophthalmics and formulations, serving regulated markets with a focus on quality. With ISO 9001:2015 certification, FDC drives innovation in generics and APIs, supported by 1,500+ distributors globally.

Our Mission

  • Deliver high-quality, affordable medicines
  • Uphold cGMP and regulatory excellence
  • Foster a quality-driven workplace

Apply urgently to roshan.bhurawane@fdcindia.com to join FDC Limited in Chhatrapati Sambhajinagar. Contribute to world-class Ophthalmic manufacturing and advance your career!

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