Accuprec Research Labs Hiring for Multiple roles in Analytical Development, Validation, and Research

Accuprec Research Labs Pvt. Ltd. is actively hiring skilled candidates for multiple roles in Analytical Development, Validation, and Research at its Ahmedabad location. If you have relevant qualifications and industry experience, this is a great opportunity to join a leading pharmaceutical research organization.

About Accuprec Research Labs

Accuprec Research Labs Pvt. Ltd. is a well-established contract research organization (CRO) specializing in analytical method development, validation, and regulatory services. The company provides high-quality analytical solutions to the pharmaceutical, biotech, and healthcare industries. Accuprec is known for its commitment to excellence and adherence to global regulatory standards, including USFDA, MHRA, and EU guidelines.

Current Openings at Accuprec Research Labs

1. Research Associate / Senior Research Associate (Analytical Development & Validation)

• Qualification: MSc. / M.Pharm or equivalent
• Experience: 3-5 years
• Key Responsibilities:
  • Analytical method development using HPLC, UHPLC, ICP-OES/MS, Ion Chromatography.
  • Analytical method validation of various methodologies.
  • Dissolution method development and validation.
  • Preparation of validation and method development protocols & reports.

2. Research Associate / Senior Research Associate (Reviewer)

• Qualification: MSc. / M.Pharm or equivalent
• Experience: 5-7 years
• Key Responsibilities:
  • Review of analytical data related to development and validation.
  • Ensuring accuracy and completeness of analytical reports.
  • Reviewing protocols and calculation sheets for validation studies.
  • Providing guidance to the analytical team.

3. Manager (LC, LC-MS)

• Qualification: MSc. / M.Pharm or equivalent
• Experience: 10+ years
• Key Responsibilities:
  • Supervising analytical method development and validation.
  • Leading a team for method validation, technology transfer, forced degradation studies, and pre-formulation studies.
  • Handling analytical queries and regulatory requirements.
  • Developing and validating methods for Nitrosamines, NDS impurities using LC-MS/MS.
  • Ensuring compliance with regulatory guidelines.

4. Assistant Manager (GC, GC-MS)

• Qualification: MSc. / M.Pharm or equivalent
• Experience: 8-10 years
• Key Responsibilities:
  • Supervising analytical method development for residual solvents, Nitrosamine, and Extractable & Leachable (E&L) studies.
  • Reviewing analytical development/validation protocols & reports.
  • Overseeing raw analytical data reviews for development, validation, and routine analysis.
  • Reporting project status to senior management

How to Apply?

If you meet the qualifications and experience requirements for any of the above roles, apply now! Send your updated resume to career@accuprec.in with details of your current in-hand salary, expected salary, and total CTC.

For any inquiries, contact 90999 32105