Research Associate – Analytical Quality Assurance | Wockhardt

Biopractify; Chhatrapati Sambhajinagar District; On-site; INR 450,000 - 550,000; Full time

Job summary

Wockhardt invites applications for a Research Associate – Analytical Quality Assurance in Chhatrapati Sambhajinagar, Maharashtra, India. The role focuses on contributing to analytical QA activities within R&D, ensuring compliance with quality standards and GLP practices.

Ideal candidates hold a postgraduate degree (M.Sc. or M.Pharm) and 2–3 years of relevant experience, with hands-on knowledge of HPLC, GC, IR, UV and QMS documentation, and a track record in method validation and development.

Qualifications

• 2–3 years of relevant experience in analytical QA.
• Postgraduate qualification in M.Sc. or M.Pharm is required.
• Knowledge of QA/GLP practices, analytical instruments, method validation and QMS documentation.

Responsibilities

• Contribute to analytical QA activities within R&D while ensuring compliance with quality standards.
• Work with analytical instruments (HPLC, GC, IR, UV) and maintain instrument performance.
• Support analytical method validation and development activities.

Skills

Analytical QA

Laboratory instruments

Method validation

QMS documentation

Education

M.Sc.

M.Pharm

Tools

HPLC

GC

IR

UV

Job description

Research Associate – Analytical Quality Assurance | Wockhardt

Position Available: Research Associate – Analytical Quality Assurance

Function: Analytical QA | Research & Development

Experience Required: 2–3 Years

Wockhardt is looking for Analytical QA professionals to join its Research & Development team. This opportunity is suitable for candidates with experience in analytical quality assurance, laboratory instruments, method validation, and QMS documentation.

What You’ll Work On

• Analytical Quality Assurance Contribute to analytical QA activities within the Research & Development function while ensuring compliance with quality standards.
• Analytical Instruments Work with and apply knowledge of HPLC, GC, IR, UV, and other analytical instruments.
• Method Validation & Development Support activities related to analytical method validation and development.
• Quality Management Systems Handle and maintain QMS-related documents and follow established quality procedures.

Ideal Candidates

You hold a postgraduate qualification in:

• M.Sc.
• M.Pharm

Candidates should have 2–3 years of relevant experience along with knowledge of:

• QA/GLP practices
• HPLC, GC, IR, UV and other analytical instruments
• Analytical method validation and development
• QMS documentation

What You’ll Gain

• Experience in Analytical Quality Assurance and R&D
• Exposure to pharmaceutical analytical instruments and laboratory practices
• Practical experience with method validation and development
• Experience handling QMS documentation
• Opportunity to work with a global pharmaceutical organization

Location: Chhatrapati Sambhajinagar, Maharashtra, India