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.”
Key responsibilities:
- Lead and manage Cleaning Validation activities for sterile and non-sterile manufacturing facilities.
- Prepare, review, and approve cleaning validation protocols, reports, and master plans (CVMP).
- Act as Subject Matter Expert (SME) for cleaning validation across the site.
- Establish acceptable limits (MACO/PDE) and perform risk assessments for cleaning processes.
- Ensure compliance with global regulatory guidelines (USFDA, EU GMP, WHO, MHRA).
- Drive execution, monitoring, and lifecycle management of cleaning validation programs.
- Collaborate with Quality Assurance, Production, QC, Engineering, and Regulatory teams.
- Participate in and support regulatory inspections and audits, addressing observations effectively.
- Investigate cleaning failures/deviations and implement CAPA.
- Ensure alignment of cleaning validation with production operations and campaign management.
- Optimize cleaning processes to improve efficiency without compromising compliance.
- Manage change control, revalidation, and periodic review activities.
- Manage cross-functional teams and projects.
- Ensure strong adherence to data integrity (ALCOA+) and documentation practices.
