Accuprec Research Labs Pvt Ltd. is a renowned Contract Research Organization (CRO) that is FDCA approved, OECD-GLP, NABL accredited, and ISO 9001:2015 certified. With its headquarters in Ahmedabad and branch offices in Canada and the USA, Accuprec provides a broad spectrum of pharmaceutical testing solutions to both domestic and multinational clients. The company’s commitment to high-quality standards has earned it a stellar reputation in the industry. Accuprec is currently hiring for immediate joining in various roles including Research Associate, Senior Research Associate, and Manager positions at their Ahmedabad location.

Available Positions:

1. Research Associate / Senior Research Associate (Reviewer)Responsibilities:
   • Review analytical data of development and validation.
   • Review routine analysis analytical data.
   • Review analytical development protocols and reports.
   • Preparation and validation of routine calculation sheets.
   • Provide guidance and support to the analytical team during development and validation.
   • Report the project status to superior management.
   Qualifications:
   • M.Sc, M.Pharm, or an equivalent qualification.
   • 5-7 years of relevant experience.
   Skills:
   • Strong knowledge of analytical techniques.
   • Experience with analytical data review and protocol reporting.
   • Detail-oriented with strong problem-solving skills.
2. Manager (LC, LC-MS)Responsibilities:
   • Lead and supervise a team of 5-10 members in analytical development, validation, and various studies.
   • Develop and validate methods for nitrosamines, NDSRI impurities, and other molecules using LC-MS/MS.
   • Oversee method development for forced degradation studies, dissolution studies, preformulation, and extractables and leachables (E&L) studies.
   • Review development and validation protocols and reports, ensuring data reliability.
   • Ensure the accuracy and completeness of computer-processed data.
   • Report the status of projects to upper management.
   Qualifications:
   • M.Sc, M.Pharm, or an equivalent qualification.
   • 10+ years of relevant experience.
   Skills:
   • Strong leadership skills with experience managing teams.
   • Expertise in LC-MS/MS techniques and method development.
   • Excellent communication and project management skills.
3. Manager (Method Validation)Responsibilities:
   • Responsible for dissolution development for pharmaceutical formulations as per FDA, EU, TGA, and ANVISA guidelines.
   • Handle analytical method validation on HPLC, ICP-OES, ICP-MS, or through wet chemistry methods.
   • Review analytical data, protocols, and reports related to development and validation.
   • Manage stability studies for pharmaceutical formulations and medical devices in compliance with ICH and ISO standards.
   • Communicate effectively with clients regarding project progress and results.
   Qualifications:
   • M.Sc, M.Pharm, or an equivalent qualification.
   • 10+ years of relevant experience.
   Skills:
   • In-depth knowledge of method validation and pharmaceutical regulations.
   • Expertise in handling various analytical techniques, including HPLC and ICP methods.
   • Strong communication skills and client-facing experience.

How to Apply:

Interested candidates are encouraged to send their resumes to the following email address: career@accuprec.in. Please ensure to include details such as your in-hand salary, expected salary, and current CTC along with your resume. The position offers a competitive salary with no bar for the right candidate.

Important Dates:

• Last date for application: 20th February 2025

Location:

• Positions are open for the Ahmedabad location.