Exciting pharma jobs in Hyderabad! Zenotech Laboratories Limited, a subsidiary of Sun Pharmaceutical Industries Ltd, is hiring experienced professionals for Quality Assurance (Validation & IPQA) and Quality Control roles in its injectable formulations plant.
These Executive/Senior Executive/Chemist positions focus on process validation, IPQA, analytical operations, and regulatory compliance. Great opportunity for pharmaceutical careers in India in a leading injectable specialty company.
About the Company
Zenotech Laboratories Limited, established in 1989 and headquartered in Hyderabad, Telangana, is a pharmaceutical specialty generic injectables company. It specializes in manufacturing and marketing oncology, biotechnology, and general injectable products.
As a subsidiary of Sun Pharmaceutical Industries Ltd (one of India’s largest pharma companies), Zenotech benefits from strong regulatory backing, advanced manufacturing capabilities, and focus on quality generics.
The facility at Turkapally operates in a cGMP-compliant environment, emphasizing data integrity, validation, and global standards for injectable formulations.
Job Details
- Company Name: Zenotech Laboratories Limited (Subsidiary of Sun Pharma)
- Experience: 5–8 years (role-specific)
- Qualification: M.Pharm / B.Pharm / M.Sc. (Organic Chemistry)
- Location: Turkapally (V), Shamirpet (M), Medchal-Malkajgiri (D), Hyderabad, Telangana – 500101
- Work Type: On-site (Injectable Formulations Plant)
Job Description
Zenotech is recruiting for key roles in Quality Assurance and Quality Control departments, supporting injectable manufacturing (aseptic processing). Positions require expertise in validation, IPQA, analytical testing, and QMS in a regulated pharma environment.
These are ideal for professionals experienced in injectables, data integrity, and GMP compliance.
Quality Assurance – Executive (Validation)
- Department: Quality Assurance
- Sub Department: Validation
- Role: Process & equipment validation, QMS oversight
- Experience: 5–7 years
- Education/Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Quality Assurance – Executive (IPQA)
- Department: Quality Assurance
- Sub Department: IPQA
- Role: In-process quality assurance for injectables
- Experience: 5–7 years
- Education/Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Quality Control – Executive/Senior Executive / Chemist
- Department: Quality Control
- Role: Analytical testing and method activities
- Experience: 6–8 years
- Education/Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Skills / Qualifications
- Expertise in process validation, cleaning validation, media fill (aseptic), data integrity (DI)
- Knowledge of Quality Management Systems (QMS), deviations, CAPA, audit readiness
- Experience with equipment/utility/HVAC/water system/facility validation, Computer System Validation (CSV)
- Hands-on operation, calibration, maintenance of GC, HPLC, and other analytical instruments
- Proficiency in analysis of raw materials, finished products, cleaning, stability samples
- Support for AMT/AMV (Analytical Method Transfer/Validation) for drug substances/products
- Review of analytical results, COA preparation, analyst qualification/training
- Handling OOS/OOT investigations, incidents, deviations, GLP/GMP compliance
- Leadership in QA teams, continuous improvement, BMR/BPR review & approval
- Strong documentation skills, cGMP/GDP adherence
Key Responsibilities
- Execute process/cleaning validation, media fill, and CSV activities
- Oversee IPQA during injectable manufacturing and packaging
- Review/approve BMR/BPR and ensure cGMP/GDP compliance
- Handle deviations, CAPA, QMS, and audit preparations
- Operate/calibrate analytical instruments (GC, HPLC etc.)
- Perform RM/FP/cleaning/stability sample analysis
- Maintain logbooks, calibration records, and test data sheets
- Prepare/qualify working/reference/primary standards
- Support AMT/AMV, review results, compile reports, issue COAs
- Conduct analyst training, investigations (OOS/OOT/incidents)
- Lead continuous improvement and team initiatives
Benefits / Perks
- Career growth in a Sun Pharma subsidiary with global standards
- Exposure to injectable manufacturing and regulatory compliance
- Opportunities for skill development in validation and analytics
- Stable environment in a leading pharmaceutical group
- Competitive compensation and professional advancement
How to Apply
Follow these steps to apply:
Step 1: Click and submit your details via the online form: https://forms.office.com/r/Y5XkYcUKKY Step 2: Email your updated resume to [email protected]
For more pharma jobs in Hyderabad, Telangana, and updates on QA/QC roles, visit trusted platforms like Pharma Recruiter.
Work Location
Zenotech Laboratories Limited Turkapally (V), Shamirpet (M), Medchal – Malkajgiri (D) – 500101 Hyderabad, Telangana State
Why You Should Join Zenotech Laboratories
Zenotech, backed by Sun Pharma, provides a robust platform for professionals in injectables and quality functions. With emphasis on innovation, data integrity, and regulatory excellence, it offers job stability, exposure to advanced aseptic technologies, and growth in a reputed group.
Ideal for those seeking impactful roles in high-quality generic injectables serving critical therapeutic areas like oncology.
FAQs
Who is eligible for Zenotech Laboratories jobs?
Candidates with 5–8 years experience in pharma (preferably injectables), M.Pharm/B.Pharm/M.Sc. Organic Chemistry, skilled in validation, IPQA, or QC analytics.
How do I apply for these QA/QC positions?
Submit details through the Microsoft Form link and email resume to [email protected].
What is the work location?
Turkapally, Shamirpet, Hyderabad, Telangana – focused on injectable formulations.
What growth opportunities are there?
Strong potential in the Sun Pharma ecosystem with exposure to global standards, validation expertise, and leadership roles in QA/QC.