Executive

SUN PHARMA; Vadodara; On-site; INR 380,000 - 700,000; Full time

Job summary

Sun Pharma in Baroda seeks an Executive – Analytical Development to support regulatory submissions and ensure cGMP-compliant analytical work. The role involves direct participation in calibration of lab equipment, analytical studies, and method development with adherence to SOPs.

Ideal candidates hold an M. Pharm with 0–4 years of experience, and will receive training to grow in the Regulatory Affairs domain within Sun Pharma.

Qualifications

• M. Pharm degree or equivalent with relevant regulatory exposure.
• Familiarity with cGMP and SOPs.
• Experience with analytical studies and method development will be preferred.

Responsibilities

• Adhere to cGMP and current SOPs for all activities.
• Complete required training prior to execution of tasks.
• Carry out analytical and physiochemical studies for regulatory submissions.
• Calibrate lab instruments (balance, pH meter, LC, GC, KF, coulometer, auto-titrator).
• Engage in method development and plant troubleshooting as needed.
• Qualify reference standards and maintain calibration and reports.

Skills

cGMP

Calibration

Analytical Studies

Method Development

SOP Compliance

Safety Procedures

Education

M. Pharm

Tools

Balance

pH meter

LC

GC

KF

Coulometer

Auto-titrator

Job description

Job Title

Executive – Analytical Development

Business Unit

R&D1 Regulatory Affairs

Job Grade

G12A

Location :

Baroda

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.

Job Description

• To work as per cGMP and ensure its compliance as per current guideline and SOPs
• Responsible to take training before execution of allotted work
• Responsible to perform analytical study and physiochemical studies samples related to regulatory submission purpose
• Responsible to perform the calibration of lab instruments like balance, pH meter, LC, GC, KF, coulometer and Auto-titrator.
• Responsible to perform the method development activity and plant trouble shooting activity.
• Responsible for qualification of reference standards/ working standard/ chemical reference standards / Global reference standard.
• Responsible for preparation of Study Protocols and Reports, Calibration reports, SOPs.
• Responsible to maintain instrument/equipment as per SOPs.
• Responsible to inform any non-compliance/event occur during execution of GMP activities.
• Responsible to follow safety precaution as per laboratory procedure

Travel Estimate

NA

Job Requirements

Educational Qualification

M. Pharm

Experience

Tenure : 0 – 4 yrs.

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together

Disclaimer:

The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)