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Otsuka Pharmaceutical India Private Limited (OPI), a fully-owned subsidiary of Japan’s Otsuka Pharmaceutical Factory, Inc., is hosting a Walk-In Interview for Quality Control (QC) Process Incharge positions on April 26, 2025, at our state-of-the-art manufacturing facility in Ahmedabad, Gujarat.
As a leader in Intravenous (IV) and parenteral nutrition products, OPI operates a USFDA, MHRA, and EU-GMP approved plant, exporting to 55+ countries. Rated 4.2/5 on AmbitionBox for job security and 4.1/5 for work-life balance, OPI offers a dynamic environment for professionals with expertise in parenteral/injectable formulations.
Join us to contribute to our mission of “creating new products for better health worldwide”
Why Work at Otsuka Pharmaceutical India?
OPI’s Ahmedabad facility, located near Bavla, specializes in sterile manufacturing of IV fluids, clinical nutrition, and infusion products. With 900+ employees and a 4.0/5 work culture rating, OPI provides a supportive workplace with six weekends off monthly and good canteen facilities.
While career growth is rated moderate at 3.4/5, employees value the relaxed environment and job stability. OPI’s commitment to cGMP compliance and innovation makes it ideal for QC professionals seeking hands-on experience in regulated markets.
- Work in a USFDA, MHRA, and EU-GMP compliant facility with global reach
- Contribute to critical parenteral products, including BFLUID and CELEMIN Infant
- Benefit from a collaborative culture with exposure to advanced QC instruments (HPLC, GC, UV)
- Join a company with a 100-year legacy, prioritizing integrity and patient well-being
Walk-In Interview Details
- Date: April 26, 2025 (Saturday)
- Time: 9:30 AM – 3:00 PM
- Venue: Otsuka Pharmaceutical India Pvt. Ltd., 21st Floor, B-Block, Westgate, Near YMCA Club, S.G. Highway, Ahmedabad, Gujarat 380015
- Job Location: Ahmedabad, Gujarat (manufacturing facility near Bavla)
Requirements:
- Updated resume
- Passport-size photograph
- Original and photocopies of educational certificates (B.Sc., B.Pharm, M.Sc.)
- Experience certificates and relieving letters
- Latest salary slip and CTC breakup
- Aadhar and PAN card copies
Eligibility:
- 2–7 years of experience in Quality Control (parenteral/injectable exposure preferred)
- Male candidates only (due to rotational shifts)
- Experience in USFDA/MHRA-regulated pharma facilities
- Candidates who attended an OPI interview in the last 6 months are not eligible
Contact:
- Freshers email CVs to anee.silas@otsukapharma.in
- Experienced candidates email CVs to hrm.opmf-amd@otsukapharma.in if unable to attend, with subject line “QC Process Incharge – Walk-In April 2025”
- Call +91-2717-678201 for inquiries
Note:
- OPI does not charge fees for job applications or interviews. Beware of fraudulent communications; verify via hrm.opmf-amd@otsukapharma.in or www.otsukapharma.in.
- Positions involve rotational shifts; only candidates with pharma exposure will be considered.
- Arrive in formal attire by 9:30 AM for registration.
Open Position
Quality Control – Process Incharge (IPPT/FP, RM/PM, Stability, Microbiology)
- Qualification: B.Sc. (Chemistry, Microbiology, Biotechnology) / B.Pharm / M.Sc. (Chemistry, Microbiology, Biotechnology)
- Experience: 2–7 years in QC for parenteral/injectable formulations
Skills Required:
- Hands-on expertise in HPLC, GC, UV-Vis Spectrophotometer, FTIR, and dissolution testing for In-Process Product Testing (IPPT) and Finished Product (FP)
- Proficiency in Raw Material (RM), Packing Material (PM), and Stability Studies analysis
- Knowledge of microbiological testing (MLT, BET, sterility, environmental monitoring) for Microbiology section
- Familiarity with cGMP, GLP, GDP, and regulatory guidelines (USFDA, MHRA, ICH)
- Experience with QMS (OOS, OOT, deviations, CAPA) and LIMS software
- Strong documentation skills and audit readiness (BMR/BPR review, SOP preparation)
Responsibilities:
- Conduct QC testing for RM, PM, IPPT, FP, and stability samples per pharmacopeial standards (USP, EP)
- Perform microbiological assays (sterility, BET, MLT) and environmental monitoring in cleanrooms
- Ensure compliance with cGMP and GDP during sampling, testing, and documentation
- Investigate deviations, OOS, and OOT results, implementing CAPA as needed
- Maintain and calibrate QC instruments, ensuring data integrity
- Support regulatory audits and coordinate with QA, production, and stores departments
How to Apply
Attend the walk-in interview on April 26, 2025, from 9:30 AM to 3:00 PM at Otsuka Pharmaceutical India Pvt. Ltd., Westgate, Ahmedabad. Bring all required documents and ensure prior experience in parenteral/injectable QC. If unable to attend, email your resume to hrm.opmf-amd@otsukapharma.in. Freshers should send CVs to anee.silas@otsukapharma.in. Visit www.otsukapharma.in for more details.
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Join OPI’s Mission!
Be part of a leading pharmaceutical company pioneering IV and parenteral nutrition solutions. At Otsuka Pharmaceutical India, your expertise as a QC Process Incharge will ensure the highest quality standards in our Ahmedabad facility, impacting patients across 55+ countries. We look forward to meeting you on April 26, 2025!