India's DMPLOI - Jobs & Networking AppWockhardt Research Centre has announced a hiring opportunity for the position of Research Associate – Analytical Quality Assurance. This is an excellent opportunity for experienced professionals with expertise in analytical research, quality assurance, and pharmaceutical laboratory operations. Candidates with M.Sc or M.Pharm qualifications and relevant analytical QA experience are encouraged to apply.
If you have hands-on knowledge of analytical instruments, method validation, and GLP compliance, this role offers the chance to work with one of India’s leading pharmaceutical research organizations.
Job Overview
Particular Details
Company Name
Wockhardt Research Centre
Position
Research Associate – Analytical Quality Assurance
Department
Analytical QA Research & Development
Job Location
Chhatrapati Sambhajinagar, Maharashtra
Experience Required
2–3 Years
Qualification
M.Sc / M.Pharm
Employment Type
Full-Time
About Wockhardt
Wockhardt Limited is a globally recognized pharmaceutical and biotechnology company known for innovation in research, manufacturing, and healthcare solutions. The company focuses on quality, integrity, patient care, and scientific excellence while developing world-class pharmaceutical products.
Key Responsibilities
Selected candidates will be responsible for:
Ensuring compliance with Quality Assurance (QA) and Good Laboratory Practices (GLP).
Performing analytical quality assurance activities in the Research & Development department.
Operating and reviewing analytical data generated from instruments such as HPLC, GC, UV, IR, and other analytical equipment.
Supporting analytical method development and validation.
Maintaining and reviewing QMS (Quality Management System) documentation.
Following company SOPs, regulatory guidelines, and quality standards.
Coordinating with R&D teams for analytical investigations and documentation.
Required Technical Skills
Candidates should possess knowledge of:
HPLC (High Performance Liquid Chromatography)
Gas Chromatography (GC)
UV-Visible Spectroscopy
Infrared Spectroscopy (IR)
Analytical Method Development
Method Validation
GLP & GMP Documentation
QMS Documentation
Pharmaceutical Quality Assurance
Laboratory Data Integrity
Educational Qualification
Applicants should have:
M.Sc in a relevant science discipline or
M.Pharm from a recognized university.
Experience
2–3 years of relevant experience in Analytical Quality Assurance or Analytical Research & Development within the pharmaceutical industry.
Job Location
Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
How to Apply
Interested candidates can send their updated CV to:
DSuryawanshi@wockhardt.com
VKakde@wockhardt.com
Email Subject Example: Application for Research Associate – Analytical Quality Assurance
Why Join Wockhardt?
Work with a globally recognized pharmaceutical company.
Exposure to advanced analytical laboratories.
Opportunity to work on research-driven pharmaceutical projects.
Career growth in Quality Assurance and R&D.
Professional learning environment with industry experts.
Technical FAQs
1. What analytical instruments should candidates be familiar with?
Candidates should have practical knowledge of HPLC, GC, UV, IR, and other pharmaceutical analytical instruments used for testing and quality assurance.
2. What is Analytical Method Validation?
Analytical Method Validation is the documented process of proving that an analytical method consistently produces reliable, accurate, precise, and reproducible results as per ICH guidelines.
3. Why is GLP important in pharmaceutical laboratories?
Good Laboratory Practice (GLP) ensures laboratory work is performed consistently, maintains data integrity, improves reliability, and complies with regulatory standards.
4. What is the purpose of QMS documentation?
Quality Management System (QMS) documentation maintains SOPs, deviations, CAPA, change controls, training records, and audit documentation to ensure compliance and product quality.
5. What skills are important for an Analytical QA Research Associate?
Important skills include analytical instrument handling, method validation, data interpretation, documentation, regulatory compliance, problem-solving, attention to detail, and knowledge of pharmaceutical quality systems.
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