Indoco Remedies Ltd., a leading Indian pharmaceutical company with over seven decades of presence and approvals from global regulatory bodies like USFDA and UKMHRA, is hosting Walk-In Interviews for its Sterile Formulations facilities. We are seeking experienced professionals to join our teams in Microbiology, Production, Quality Assurance (QA), Quality Control (QC), and Shift Incharge/Line Incharge roles across Hyderabad, Goa, and Maharashtra. With a global footprint in 55 countries and a USD 166 million valuation, Indoco offers a dynamic work environment for career growth.
Interview Details
- Dates and Venues:
- Hyderabad: Sunday, April 27, 2025
- Time: 9:00 AM to 6:00 PM
- Venue: The Elite Hotel, Gachibowli – Miyapur Road, Hafeezpet, Hyderabad, Telangana 500050
- Goa: Sunday, May 18, 2025
- Time: 9:00 AM to 6:00 PM
- Venue: Indoco Remedies Limited, Plant-II, L-32, 33, 34, Verna Industrial Estate, Verna, Goa 403722
- Maharashtra: Sunday, June 1, 2025
- Time: 9:00 AM to 6:00 PM
- Venue: Hotel Freesia by Express Inn, Next to Big Bazar, Ostwal Empire, Boisar – Tarapur Road, Boisar, Maharashtra 401501
- Hyderabad: Sunday, April 27, 2025
- Documents Required:
- Updated resume
- Copy of Aadhar Card and PAN Card
- Recent increment letter and salary structure
- Educational certificates
- Contact:
- Email: hrd2@indoco.com or career@indoco.com
- Phone: +91 832-6624209 / +91 70300 51326 / +91 73910 54322
- Note:
- Vacancy Notification: RQ250032248
- Only experienced candidates should attend; freshers may email CVs to the above addresses.
- Candidates must be willing to work in shifts.
- Subsidized transport facilities provided from Margao, Vasco, Ponda, Mapusa, Panjim, Sanquelim, Bicholim, Marcel, and Cortalim for Goa-based roles.
Why Join Indoco Remedies?
Indoco Remedies is a fully integrated, research-oriented pharmaceutical company with nine manufacturing facilities, including USFDA-approved sterile plants in Goa. With 6,000+ employees, including 300+ scientists, we are committed to excellence in sterile formulations (injectables and ophthalmics). Benefits include:
- Work in state-of-the-art, cGMP-compliant facilities approved by USFDA, UK-MHRA, and TGA-Australia
- Opportunities for career growth in a company rated 3.6/5 on AmbitionBox for work culture
- Five-day workweek, cultural events, and a supportive environment, particularly for women employees
- Exposure to global markets and regulatory audits (USFDA, MHRA)
Note: Some employee reviews mention challenges with internal politics and appraisal processes, suggesting candidates clarify growth opportunities during interviews.
Available Positions
1. Microbiology – Officer / Senior Officer / Senior Executive
- Experience: 3–8 years
- Qualification: B.Sc. / M.Sc. (Microbiology / Biotechnology)
- Job Profile:
- Conduct environmental monitoring, routine and non-routine analysis
- Perform Process Efficacy Testing (PET), sterility testing, Bacterial Endotoxin Testing (BET), and water testing
- Manage Quality Management Systems (QMS) documentation
- Experience in injectable/ophthalmic products required
- Key Skills:
- Knowledge of cGMP and aseptic techniques
- Familiarity with regulatory audits (USFDA, MHRA)
- Proficiency in microbiological testing protocols
- Open Positions: Multiple
2. Production – Officer / Executive
- Experience: 2–6 years
- Qualification: B.Sc. / B.Pharm / M.Pharm
- Job Profile:
- Handle manufacturing, filling, washing, autoclave, and isolator operations for injectable/ophthalmic products
- Manage QMS documentation and compliance
- Execute aseptic processes and equipment cleaning
- Key Skills:
- Expertise in sterile manufacturing and cGMP
- Experience with vial filling, isolators, and autoclaves
- Strong documentation and troubleshooting skills
- Open Positions: Multiple
3. Quality Assurance (QA) – Junior Officer / Senior Executive
- Experience: 3–12 years
- Qualification: M.Pharm / B.Pharm
- Job Profile:
- Perform In-Process Quality Assurance (IPQA) for injectables
- Conduct process and cleaning validation
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
- Manage qualification reviews and QMS activities
- Monitor aseptic core areas
- Key Skills:
- Strong knowledge of cGMP, QMS, and validation protocols
- Experience with regulatory audits and documentation
- Attention to detail and compliance focus
- Open Positions: Multiple
4. Quality Control (QC) – Officer
- Experience: 3–5 years
- Qualification: B.Sc. / M.Sc. (Chemistry)
- Job Profile:
- Perform analysis using HPLC, UV, Karl Fischer, Autotitrator, GC, and dissolution testing for sterile and non-sterile products
- Conduct stability studies and validation
- Ensure compliance with Good Laboratory Practices (GLP)
- Key Skills:
- Proficiency in analytical instruments (HPLC, GC, UV)
- Knowledge of cGMP and regulatory requirements
- Experience in sterile product analysis
- Open Positions: 77
5. Shift Incharge / Line Incharge – Senior Executive
- Experience: 2–10 years
- Qualification: B.Pharm / M.Pharm
- Job Profile:
- Oversee manufacturing, filling, washing, and isolator operations for injectable/ophthalmic products
- Manage shift operations and ensure QMS compliance
- Coordinate with teams to meet production targets
- Key Skills:
- Leadership and team management skills
- Expertise in sterile manufacturing and cGMP
- Experience with QMS and regulatory audits
- Open Positions: Multiple
How to Apply
- Walk-In: Attend the interview at the specified venue, date, and time with all required documents.
- Email Application: If unable to attend, send your CV to hrd2@indoco.com or career@indoco.com with the subject line “Application for [Position] – [Location]” (e.g., “Application for Microbiology Officer – Hyderabad”).
- Registration: No prior registration is required for the walk-in, but emailing CVs in advance is recommended.
Application Deadline
- Hyderabad: April 27, 2025
- Goa: May 18, 2025
- Maharashtra: June 1, 2025
- Email applications are accepted on a rolling basis.
Contact Us
- Email: hrd2@indoco.com / career@indoco.com
- Phone: +91 832-6624209 / +91 70300 51326 / +91 73910 54322
- Website: www.indoco.com
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Additional Information
- Company Background: Indoco Remedies operates nine manufacturing facilities, including a USFDA-approved sterile plant (Plant-II) in Verna, Goa, designed with modular layouts, SCADA systems, and HVAC maintaining 55% ± 5% humidity. The company exports generics to regulated markets and employs 6,000+ personnel.
- Employee Feedback: Reviews highlight a five-day workweek and women-friendly policies but note challenges with internal politics and appraisal fairness. Candidates should discuss career progression during interviews.
Location Context:
- Hyderabad: The Elite Hotel is centrally located in Hafeezpet, a hub for IT and pharma industries, ensuring easy access.
- Goa: Plant-II in Verna Industrial Estate is a non-pollutant area with advanced sterile facilities.
- Maharashtra: Boisar is a key industrial hub, with the venue near major pharma clusters like Tarapur.
Join Indoco Remedies Ltd. and contribute to our mission of delivering high-quality sterile formulations globally. We look forward to meeting experienced professionals ready to make an impact! 🌍