𝗧𝗵𝗶𝘀 𝗿𝗼𝗹𝗲 𝗶𝘀 𝗳𝗼𝗿 𝗼𝗻𝗲 𝗼𝗳 𝘁𝗵𝗲 𝗪𝗲𝗲𝗸𝗱𝗮𝘆'𝘀 𝗰𝗹𝗶𝗲𝗻𝘁𝘀

𝗦𝗮𝗹𝗮𝗿𝘆 𝗿𝗮𝗻𝗴𝗲: 𝗥𝘀 𝟭𝟬𝟬𝟬𝟬𝟬 - 𝗥𝘀 𝟰𝟬𝟬𝟬𝟬𝟬 (𝗶𝗲 𝗜𝗡𝗥 𝟭-𝟰 𝗟𝗣𝗔)

Experience: 1+ yrs

Location: Gujarat

As an ADL Associate, you will work closely with analytical development, formulation development, and quality control teams to support the testing and evaluation of pharmaceutical formulations. You will assist with analytical method development, testing, documentation, and laboratory operations while ensuring compliance with applicable quality standards and standard operating procedures.

This role offers an opportunity to develop your technical expertise in pharmaceutical analytical development and contribute to formulation research and development activities.

Requirements

Key Responsibilities

• Support analytical development activities for pharmaceutical formulations.
• Perform analytical testing of formulation samples according to approved methods and established procedures.
• Assist in analytical method development, optimization, and validation activities under the guidance of senior team members.
• Prepare, review, and maintain laboratory records, analytical reports, and technical documentation.
• Ensure compliance with Good Laboratory Practices (GLP), applicable GMP requirements, and standard operating procedures (SOPs).
• Coordinate with formulation development and quality control teams to support project requirements.
• Assist in investigating analytical discrepancies and documenting observations, as required.
• Ensure proper handling of laboratory equipment, chemicals, reagents, and samples.
• Maintain data accuracy, integrity, and traceability throughout analytical activities.
• Complete assigned tasks within established timelines while adhering to laboratory safety and quality standards.

What Makes You a Great Fit?

• Bachelor's or Master's degree in Pharmacy, Pharmaceutical Chemistry, Analytical Chemistry, or a related discipline.
• Minimum of 1 year of relevant experience in an Analytical Development Laboratory (ADL), preferably within pharmaceutical formulation development.
• Basic understanding of analytical testing techniques and pharmaceutical analysis.
• Familiarity with analytical method development, validation, and laboratory documentation.
• Knowledge of GLP, GMP, SOPs, and laboratory safety practices.
• Strong analytical, documentation, and problem-solving skills.
• Excellent attention to detail and commitment to data integrity and quality compliance.
• Ability to collaborate effectively with cross-functional teams and meet project deadlines.
• Willingness to work at the company's facility in Gujarat.
• Current or expected CTC within the budget of ₹1–4 LPA.