Sr. Executive- MSTG

Sun Pharma

Kalol

On-site

INR 1,400,000 - 2,200,000

Full time

8 days ago

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Job summary

Sun Pharma is seeking an experienced professional to lead technology transfer activities for solid oral dosage forms, coordinating scale-up, exhibit, and process validation batches with optimal use of resources. You will troubleshoot during batch execution, analyze data, and investigate deviations.

Maintaining strict cGMP compliance and regulatory documentation is essential, with cross-functional collaboration across teams.

Qualifications

  • Master degree in a relevant field.
  • 7+ years of experience in technology transfer or related field.

Responsibilities

  • Execute technology transfer activities for solid oral dosage forms, including planning and performing scale-up, exhibit, and process validation batches with efficient utilization of manpower, materials, and equipment.
  • Provide technical support for troubleshooting during batch execution, perform data comparisons, and conduct root cause investigations for deviations and process issues at Sun Pharma or CMOs.
  • Ensure compliance with cGMP and regulatory requirements while preparing and reviewing related documentation, coordinating with cross-functional teams to achieve seamless transfer and validation outcomes.

Education

Master Degree

Job description

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
  1. Responsible for executing technology transfer activities for solid oral dosage forms, including planning and performing Scale-up, Exhibit and Process Validation batches with optimal utilization of manpower, materials, and equipment.
  2. Provide technical support for troubleshooting during batch execution, conduct data comparison, and perform root cause investigations for deviations and process issues at Sun Pharma or CMOs.
  3. Ensure compliance with cGMP and regulatory requirements while preparing and reviewing all related documentation, and coordinate effectively with cross-functional teams to achieve seamless technology transfer and validation outcomes.
Educational Qualification
  • Master Degree
Experience
  • Minimum 7 years of relevant experience
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