Research Associate (Research & Development)

Vasant Chemicals; Hyderabad; On-site; INR 500,000 - 800,000; Full time

Job summary

Vasant Chemicals in Hyderabad, India, seeks a motivated Research Associate to support formulation development, laboratory testing, analytical studies, and product improvement while ensuring quality and regulatory compliance. The role involves collaborating with QA, Regulatory Affairs, and Production to advance pipeline projects and scale-up activities.

Ideal candidates have 3–5 years in Pharmaceutical or Chemical R&D, hands-on formulation experience, and a strong ability to document findings

Qualifications

• 3–5 years of experience in Pharmaceutical or Chemical R&D.
• Experience in formulation development and laboratory operations.
• CDMO/CRO exposure preferred but not required.

Responsibilities

• Support formulation development and product improvement projects.
• Perform laboratory experiments and evaluate formulation performance.
• Assist in developing new products and optimizing existing formulations.
• Conduct routine laboratory testing and maintain equipment calibration.
• Ensure GMP/GLP compliance and proper documentation.

Skills

Formulation Development

Laboratory Operations

Analytical Testing

GLP/GMP Compliance

Data Interpretation

Documentation

Education

B.Pharm / M.Pharm or BSc/MSc in Chemistry

Job description

We are looking for a motivated and detail-oriented Research Associate to join our Research & Development team. The candidate will support formulation development, laboratory testing, analytical studies, and product improvement initiatives while ensuring compliance with quality and regulatory standards.

Candidates with prior experience in CDMO (Contract Development and Manufacturing Organization) or CRO (Contract Research Organization) environments will be given preference.

Key Responsibilities

Research & Development

• Support formulation development and product improvement projects.
• Perform laboratory experiments and evaluate formulation performance.
• Assist in developing new products and optimizing existing formulations.

Laboratory Operations

• Conduct routine laboratory testing and experimental work.
• Maintain laboratory equipment and ensure proper calibration.
• Follow laboratory safety protocols and Good Laboratory Practices (GLP).

Analytical Testing

• Perform analytical testing using standard laboratory techniques and instruments.
• Interpret experimental results and prepare technical reports.
• Maintain accurate documentation of research findings and observations.

Quality & Compliance

• Ensure compliance with GMP, GLP, SOPs, and quality standards.
• Support validation studies and stability testing activities.
• Maintain laboratory documentation in accordance with regulatory requirements.

Documentation & Reporting

• Record experimental data accurately.
• Prepare technical reports, protocols, and research documentation.
• Present findings to the R&D team and management when required.

Cross-functional Coordination

• Collaborate with Quality Control, Production, Regulatory Affairs, and Product Development teams.
• Support technology transfer and scale-up activities where applicable.

Required Skills

• Research & Development (R&D)
• Formulation Development
• Laboratory Operations
• Analytical Testing
• Quality Control
• Data Interpretation
• Technical Documentation
• GMP & GLP Compliance
• Problem Solving
• Attention to Detail

Preferred Candidate Profile

• 3-5 years of experience in Pharmaceutical or Chemical Research & Development.
• Experience in formulation development and laboratory operations.
• Prior experience in CDMO/CRO organizations will be highly preferred.
• Good understanding of analytical techniques and quality systems.
• Strong analytical, documentation, and communication skills.
• Ability to work independently as well as in a collaborative team environment.

Qualification

Bachelor's or Master's Degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering, Life Sciences, or a related discipline.

Notice Period

Immediate Joiners / 0-30 Days / Candidates Currently Serving Notice Period