Easter Seals Jobs

Qualification - MSc/BSc

Experience - 8-10 years

Job Responsibilties:

1. Responsible for monitoring of all cGMP activities at site.

2. Facilitate review and support regulatory inspection management.

3. To have the oversight, monitoring and compliance with all quality systems at the site.

4. Monitoring and tracking of various compliance actions arises due to regulatory inspections and intimal\customer audits.

5. Draft, facilitate and ensure timely inspection response and monitor CAPA timelines.

6. Support for major health authority inspections at site and provide input and support to inspection responses to drive consistency and clarity at the site.

7. Collaborate with Corporate compliance group and implement global CAPA.

8. To extend support for Implementation of effective GQSs/GSOPs

9. To extend support for Coordination & closure of Field Alert Report.

10. Toparticipateinaprocessforsimplificationofmanufacturing&qualitysite procedurestoreduce complexity.

11. Provide support in execution and monitoring of remediation compliance through compliance verification audits.

12. Responsible for all compliance and bringing solutions to compliance related issues within the site.

13. To perform GMP round for General Tablets, Cyto, SH, Aerosol and QC non sterile manufacturing/laboratory area.

14. To extend support for tracking & closure of open QMS for non-sterile manufacturing/Laboratory areas.

15. Handling of internal and external quality audit.

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.