At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering
an workplace 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:
* Responsible for monitoring of all cGMP activities at site.
* Facilitate review and support regulatory inspection management.
* Monitoring and tracking of various compliance actions arises due to
regulatory inspections and internalcustomer audits.
* Draft, facilitate and ensure timely inspection response and monitor CAPA
timelines.
* Collaborate with Corporate compliance group and implement global CAPA.
* Facilitate, review and monitor cross functional investigation teams.
* Support plant for management of compliance activities.
* Regularly evaluate and report compliance status of site to Site Quality Head.
* Support for major health authority inspections at site and provide input and
support to inspection responses to drive consistency and clarity at the site.
* Support compliance investigations as needed in collaboration with others at
the site.
* Provide oversight of quality activity outcomes resulting from regulatory
inspections, commitments and filings.
* Provide support in execution and monitoring of remediation compliance through
compliance verification audits.
* Responsible for all compliance and bringing solutions to compliance related
issues within the site.
* Review Regulatory inspection observations, trend and decide compliance
strategy.
* Educate and institutionalize a culture of Qu