Apply for high-paying Quality Assurance (QC Reviewer) jobs at Zenotech Laboratories (Sun Pharma) in Hyderabad. Join a USFDA-approved sterile injectables facility. 2-5 years of pharma QA experience required. Apply today!
Zenotech Laboratories (Sun Pharma) Hiring for High-Paying Quality Assurance (QC Reviewer) Jobs in Hyderabad 2025
Are you looking for high-paying pharma jobs in India 2025? Do you have expertise in pharmaceutical Quality Assurance (QA), QC reviewing, and regulatory compliance? Here’s a golden opportunity to join Zenotech Laboratories, a Sun Pharma company, and accelerate your pharmaceutical career with one of India’s leading USFDA-regulated sterile injectables manufacturing facilities.
Zenotech Laboratories, based in Hyderabad, Telangana, is now hiring for Quality Assurance (QC Reviewer) roles across Sr. Officer, Officer, and Jr. Officer positions. If you have 2-5 years of relevant QA experience in pharma QC review processes, this could be your next career breakthrough.
About Zenotech Laboratories – A Sun Pharma Company
Zenotech Laboratories Limited is a specialized biopharmaceutical company operating under the global leadership of Sun Pharmaceutical Industries Ltd., one of the world’s largest and most respected pharmaceutical companies. Zenotech focuses on generic sterile injectables, oncology products, and biotechnology formulations for regulated international markets.
Zenotech’s Hyderabad facility is a USFDA-approved state-of-the-art sterile injectable manufacturing plant, playing a pivotal role in producing high-quality oncology and biogeneric products for global distribution. With a robust cGMP-compliant environment, advanced QMS systems like Trackwise, and regular exposure to global regulatory audits, Zenotech offers unparalleled career growth for pharmaceutical professionals.
🔎 Current Job Openings – Quality Assurance (QC Reviewer) Positions
Zenotech Laboratories is actively recruiting pharma QA professionals who possess strong technical expertise in QC documentation review, QMS compliance, and analytical report verification.
✅ Job Designation:
- Sr. Officer / Officer / Jr. Officer – Quality Assurance (QC Reviewer)
✅ Required Qualifications:
- M.Sc. (Chemistry)
- B.Pharmacy / M.Pharmacy
✅ Required Experience:
- 2-5 Years of experience in pharmaceutical Quality Assurance, specifically in QC document review within a regulated manufacturing facility.
✅ Key Responsibilities:
- Review and approve SOPs (Standard Operating Procedures), GTPs (General Test Procedures), STPs (Standard Test Procedures), and specifications to ensure accuracy and regulatory compliance.
- Verify analytical reports related to raw materials, packing materials, finished products, and stability studies.
- Conduct thorough investigations of OOS (Out of Specification), OOT (Out of Trend) deviations and incident reports.
- Perform Quality Management System (QMS) activities using advanced software like Trackwise.
- Review and maintain the integrity of electronic batch records and laboratory data.
- Ensure strict adherence to GLP (Good Laboratory Practices), cGMP guidelines, and regulatory standards.
✅ Skills and Competencies Required:
- In-depth knowledge of cGMP guidelines, regulatory compliance, and pharmaceutical quality systems.
- Hands-on experience with QMS platforms (e.g., Trackwise) for managing deviations, CAPAs, and document control.
- Proficiency in reviewing analytical data, specifications, stability reports, and laboratory investigations.
- Strong documentation, problem-solving, and communication skills.
- Prior experience in USFDA, MHRA, WHO-GMP audit environments is highly desirable.
✅ Notice Period:
- Candidates with 1-2 months notice period will be preferred.
📍 Job Location:
Zenotech Laboratories Limited
Survey No. 250-252, Turkapally (V),
Shamirpet (M), Medchal-Malkajgiri,
Hyderabad, Telangana – 500101
📩 How to Apply:
Interested candidates can email their updated resume to: hr1@zenotech.co.in
(Use subject line: “QA-QC Reviewer”)
Official Website: www.zenotechlab.com
🚀 Why Join Zenotech Laboratories (Sun Pharma)?
🌎 Global Exposure with Sun Pharma Leadership
Be part of Sun Pharma’s global network, working on sterile injectables, oncology, and biogenerics for regulated markets worldwide.
📈 Career Advancement in a USFDA-Approved Facility
Gain extensive experience handling global regulatory audits (USFDA, MHRA, WHO-GMP) in a state-of-the-art facility.
💰 High Paying Pharma Jobs in India 2025
Competitive salary packages that reflect your QA expertise, QMS proficiency, and regulatory experience.
🏢 Work-Life Balance in Hyderabad’s Pharma Hub
Enjoy a strong work culture in Hyderabad’s thriving pharmaceutical and biotech ecosystem with access to cutting-edge technologies.
🛡 Secure Long-Term Career Growth
With India’s increasing global role in biopharma and contract manufacturing, Zenotech offers job stability, career progression, and leadership opportunities.
🔑 Important Application Notes:
- Minimum 2-5 years of pharma QA experience in QC documentation review is mandatory.
- Hands-on knowledge of Trackwise, OOS/OOT investigations, and GLP compliance will be a major advantage.
- Candidates who have attended interviews at Zenotech in the last 6 months are not eligible to apply.
- Zenotech Laboratories / Sun Pharma do not charge any recruitment fees. Candidates are advised to report any suspicious activities immediately.
- Only shortlisted candidates will be contacted for further interview rounds.
📝 How to Prepare for Zenotech QA Interviews:
- Highlight your experience with SOP reviews, QMS documentation, incident investigations, and stability data verification.
- Clearly showcase your exposure to cGMP regulations and regulatory audit participation.
- Demonstrate hands-on knowledge with Trackwise or equivalent QMS tools.
- Include specific examples of analytical report reviews, OOS investigations, or process improvements you’ve led.
- Mention your notice period (1-2 months) prominently in your resume.
