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Indoco Hiring for Microbiology / Production / QA/ QC / Shift Incharge/ Line Incharge

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Indoco Remedies, a leading pharmaceutical company with a strong global presence and international regulatory approvals including USFDA and UK MHRA, is conducting a series of walk-in interviews across India for experienced professionals in sterile formulations. This is an excellent opportunity to join a reputable organization known for its commitment to quality and innovation in the pharmaceutical industry. With a rich history spanning 77 years of excellence, Indoco offers a stable and rewarding career path for dedicated individuals.

Open Positions & Requirements:

We are currently seeking highly motivated and experienced candidates for the following roles:

1. Microbiology Officer

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  • Experience: 3 to 8 years
  • Qualification: BSc/MSc (Microbiology/Biotechnology)
  • Job Profile: The ideal candidate will possess extensive experience in environmental monitoring, quality management systems (QMS), routine and non-routine microbiological analysis. Proficiency in performing tests such as pyrogen testing (PET), sterility testing, bioburden testing (BET), and water testing is essential. Specific experience with injectable and ophthalmic products is highly preferred. Strong knowledge of Good Manufacturing Practices (GMP) is also required.

Key Responsibilities:

  • Performing environmental monitoring within the sterile manufacturing facility.
  • Conducting routine and non-routine microbiological tests.
  • Ensuring compliance with relevant QMS procedures and regulatory guidelines.
  • Investigating and resolving microbiological deviations.
  • Maintaining accurate and comprehensive records.
  • Participating in internal and external audits.

2. Production Officer/Executive

  • Experience: 2 to 6 years
  • Qualification: BSc/B.Pharm/M.Pharm
  • Job Profile: Candidates should have practical experience in the manufacturing, filling, washing, and quality management systems (QMS) of injectable and ophthalmic products. Experience with autoclaves and isolators is a significant advantage. A strong understanding of aseptic processing techniques and GMP is crucial.

Key Responsibilities:

  • Overseeing production processes to meet quality and output targets.
  • Ensuring adherence to GMP standards and procedures.
  • Troubleshooting production issues and implementing corrective actions.
  • Maintaining detailed records of production activities.
  • Collaborating effectively with other departments, including Quality Assurance and Quality Control.

3. Quality Assurance Junior Officer/Senior Executive

  • Experience: 3 to 5 years
  • Qualification: BSc/MSc (Chemistry)
  • Job Profile: The successful candidate will have a thorough understanding of analytical techniques used in quality control, including HPLC, UV-Vis spectrophotometry, Karl Fischer titration, autotitration, gas chromatography (GC), and dissolution testing. Experience with sterile and non-sterile products is essential.

Key Responsibilities:

  • Performing routine and non-routine analytical testing of pharmaceutical products.
  • Ensuring the accuracy and reliability of testing results.
  • Maintaining and calibrating laboratory equipment.
  • Reviewing and approving test results.
  • Contributing to continuous improvement initiatives.

4. Quality Control Officer

  • Experience: 3 to 12 years
  • Qualification: M.Pharm/B.Pharm
  • Job Profile: This role requires significant experience in injectable IPQA (In-Process Quality Assurance), process and cleaning validation, BMR (Batch Manufacturing Records) and BPR (Batch Production Records) review, qualification review, and QMS.

Key Responsibilities:

  • Ensuring adherence to GMP standards and regulatory requirements.
  • Reviewing and approving batch records.
  • Conducting investigations into quality issues.
  • Participating in quality audits.
  • Supporting the development and implementation of quality systems.

5. Shift Incharge/Line Incharge

  • Experience: 2 to 10 years
  • Qualification: B.Pharm/M.Pharm
  • Job Profile: Candidates should have hands-on experience in the manufacturing, filling, washing, and quality management systems (QMS) of injectable and ophthalmic products, with experience in isolators a plus.

Key Responsibilities:

  • Overseeing all aspects of production during a specific shift.
  • Managing a team of production personnel.
  • Ensuring efficient and timely completion of production schedules.
  • Maintaining high standards of quality and safety.

Walk-in Interview Details:

Location 1:

  • Date: Sunday, April 27, 2025
  • Time: 9:00 AM to 6:00 PM
  • Venue: The Elite Hotel, Gachibowli – Miyapur Road, Hafeezpet, Hyderabad, Telangana – 500050

Location 2:

  • Date: 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

Location 3:

  • Date: Sunday, June 1, 2025
  • Time: 9:00 AM to 6:00 PM
  • Venue: Hotel Freesia by Express Inn, Next to BigBazar, Ostwal Empire, Boisar – Tarapur Road, Boisar, Maharashtra – 401501

Important Considerations:

  • Candidates must be willing to work in shifts.
  • Subsidized transport facilities are provided from various locations in Goa (Margao, Vasco, Ponda, Mapusa, Panjim, Sanquelim, Bicholim, Marcel, and Cortalim).
  • Only experienced candidates need apply. Please submit your CV to hrd2@indoco.com or career@indoco.com.
  • Contact Number: 08326624209 / 7030051326 / 7391054322
  • Notification of application receipt acknowledgment RQ250032248

We encourage all eligible and interested candidates to attend these walk-in interviews. Indoco Remedies offers a dynamic work environment, competitive compensation and benefits packages, and ample opportunities for professional growth. We look forward to meeting you!

Indoco Hiring for Microbiology / Production / QA/ QC / Shift Incharge/ Line Incharge