Join Indoco Remedies Limited, a leading Indian pharmaceutical company founded in 1947, headquartered in Mumbai, with a turnover of ₹1,800 Cr and a presence in 55+ countries. Renowned for its USFDA, UKMHRA, WHO-GMP, and ISO 9001:2015-certified facilities, Indoco manufactures oral solid dosages (OSD), injectables, and APIs, serving regulated markets like the USA and Europe.
We’re hosting a walk-in interview on May 17, 2025, at our Baddi, Himachal Pradesh facility (Unit-III) for Quality Control (QC), Quality Assurance (QA), and Production roles, targeting professionals and operators with 3-8 years of experience in formulation plants.
Contents
Event Details: Walk-In Interview
This walk-in interview seeks experienced candidates for QC, QA, and Production roles at our Baddi Unit-III, a key site for OSD manufacturing. Candidates with regulatory exposure to USFDA/UKMHRA are preferred.
Date and Time
- Date: Saturday, May 17, 2025
- Time: 9:00 AM – 2:00 PM IST
Interview Venue
Indoco Remedies Limited
Unit-III, Village Katha, P.O. Baddi, District Solan, Himachal Pradesh – 173205
Job Location
- Same as venue: Indoco Remedies Limited, Unit-III, Baddi, Himachal Pradesh – 173205
Job Opportunities at Indoco Remedies
We’re hiring for QC, QA, and Production roles to support formulation manufacturing at our Baddi facility, compliant with cGMP standards. All positions require experience in regulated OSD environments.
1. Quality Control (QC) – Officer / Sr. Officer
- Qualification: B.Sc. (Chemistry), M.Sc. (Chemistry, Analytical Chemistry), B.Pharm
- Experience: 3-8 years in QC for OSD formulation plants
- Key Responsibilities:
- Perform sampling, testing, and analysis of raw materials, in-process, and finished products
- Operate and calibrate instruments like HPLC, UV, IR, and dissolution testers
- Conduct stability studies and method validations per ICH Q2(R1)
- Document results in LIMS and investigate OOS/OOT incidents
- Support USFDA/UKMHRA audits with GLP compliance
- Key Skills:
- Expertise in HPLC, UV, and dissolution testing
- Knowledge of cGMP, GLP, and regulatory standards (USFDA, UKMHRA)
- Proficiency in QMS (OOS, deviations, CAPA) and LIMS
- Strong analytical and audit-facing skills
- Openings: Multiple (likely 3-5 based on QC lab needs)
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards for Baddi)
2. Quality Assurance (QA) – Officer / Sr. Officer
- Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry)
- Experience: 3-8 years in QA for OSD formulation plants
- Key Responsibilities:
- Conduct IPQA activities, line clearances, and in-process checks
- Review BMRs, BPRs, and SOPs for compliance with 21CFR Part 11
- Manage QMS processes (deviations, CAPA, change controls)
- Support cleaning validation and vendor qualifications
- Prepare for and participate in USFDA/UKMHRA audits
- Key Skills:
- Expertise in IPQA, QMS, and cleaning validation
- Knowledge of cGMP and regulatory requirements (USFDA, UKMHRA)
- Strong documentation and audit preparation skills
- Ability to handle deviations and CAPA effectively
- Openings: Multiple (likely 3-5 based on QA operations)
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards)
3. Production – Officer / Sr. Officer
- Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry)
- Experience: 3-8 years in OSD production
- Key Responsibilities:
- Supervise manufacturing operations for compression, blister packing, and autocartonator processes
- Ensure cGMP compliance and accurate BMR/BPR documentation
- Monitor in-process parameters (e.g., weight, hardness) and yield
- Troubleshoot equipment issues and coordinate with engineering teams
- Support USFDA/UKMHRA audits and process validations
- Key Skills:
- Expertise in compression (e.g., Fette, Cadmach), blister (CAM, IMA), and autocartonator machines
- Knowledge of cGMP and regulatory standards
- Strong supervisory and documentation skills
- Ability to manage production schedules and audits
- Openings: Multiple (likely 3-5 based on production lines)
- Salary: ₹4.0–8.0 Lakhs/year (estimated based on industry standards)
4. Production – Operator / Sr. Supervisor
- Qualification: 10+2, ITI (Mechanical, Electrical), Diploma (Pharmacy, Mechanical)
- Experience: 3-5 years in OSD production
- Key Responsibilities:
- Operate compression, blister packing, and autocartonator machines
- Perform line setup, cleaning, and in-process checks
- Document equipment logs and support BPR completion
- Ensure hygiene and safety standards per SOPs
- Assist in troubleshooting and maintenance activities
- Key Skills:
- Hands-on experience with compression, blister, and autocartonator equipment
- Basic understanding of cGMP and SOPs
- Precision in operational and documentation tasks
- Adaptability to shift work
- Openings: Multiple (likely 5-8 based on operator needs)
- Salary: ₹2.5–4.5 Lakhs/year (estimated based on industry standards)
Why Join Indoco Remedies?
Indoco Remedies, with 6,000+ employees, is rated 3.8/5 on AmbitionBox for job security (4.0/5 in Baddi) and 3.7/5 for work-life balance. Our Baddi Unit-III, approved by USFDA and UKMHRA, supports generics for regulated markets, specializing in tablets and capsules. Employees praise regulatory exposure (4.1/5) and learning opportunities but note moderate career growth (3.6/5). With a 77-year legacy and 9 manufacturing facilities, Indoco offers a robust platform for professional development.
Key Benefits
- Work in a USFDA/UKMHRA-approved OSD facility
- Gain expertise in HPLC, QMS, and compression processes
- Support generics for 55+ countries
- Join a company with ₹1,800 Cr turnover
- Access growth opportunities in Himachal Pradesh’s pharma hub
How to Apply
Attend the walk-in interview on May 17, 2025, from 9:00 AM to 2:00 PM at Indoco Remedies, Unit-III, Baddi. Bring:
- Updated resume (original and photocopy)
- Original certificates (B.Sc., M.Sc., B.Pharm, M.Pharm, 10+2, ITI, Diploma)
- Experience letters and last 3 months’ salary slips
- Aadhar and PAN cards
- Passport-size photographs (2)
- Preparation:
- QC: Review HPLC, UV, and ICH Q2(R1) guidelines
- QA: Study IPQA, QMS, and audit processes
- Production: Prepare for compression, blister, and cGMP standards
- Be ready to discuss USFDA/UKMHRA audit exposure
- Note: Candidates unable to attend can email CVs to avinash.kumar@indoco.com by May 15, 2025, with subject “Role Name – Baddi”. Contact Avinash Kumar at 01795-245609 for queries. Indoco Remedies does not charge recruitment fees; verify communications via @indoco.com emails.
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About Indoco Remedies
Indoco operates 9 manufacturing facilities, with Baddi Unit-III specializing in OSD formulations. With 700+ product dossiers and approvals from USFDA, UKMHRA, and TGA-Australia, we lead in anti-diabetics and ophthalmics. Our R&D center in Navi Mumbai, with 400+ scientists, drives innovation in pharmaceutical manufacturing.
Our Mission
- Deliver affordable, high-quality medicines
- Uphold cGMP and global regulatory excellence
- Foster a collaborative, growth-oriented workplace
Attend the walk-in interview on May 17, 2025, in Baddi or email avinash.kumar@indoco.com. Join Indoco Remedies’ Baddi team and advance pharmaceutical manufacturing!