Sun Pharmaceutical Industries Ltd Walk-in Interview .Sun Pharmaceutical Industries Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
- *Department :- Sr Officer QA- IPQA-API
- *Experience :- 2-5 years*
- *Qualification :- Bsc,Msc,Bpharm
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description: Greeting from Sun Pharmaceutical Industries Ltd !!!
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:
Batch Release: To perform usage decision of finished product, Intermediate and recovered solvent batches and ensure all requirements as per SOPs, Specifications, Customer & Regulatory Commitments, Exhibit / PPQ Batch Protocol (as applicable) are complied prior to taking Usage Decision on a batch.
To perform sampling and sample distribution of Finished Product & Intermediates as per SOP.
Control and review of Batch production records of APIs, intermediate & recovered solvents of all API plants.
To review of batch production records and analytical records before release of batches for distribution and to release delivery order.
Preparation and review of Annual Product Review as per SOP.
Management of Retention samples including annual inspection of API and to maintain related records.
To perform following activities in Track wise (CQMS) system as per requirement.
-Sampling investigation
-QA review and verification tasks
-Initiation of change controls and investigation/deviation.
To perform environmental monitoring of general API plants, preparation and review of trend and its evaluation as per SOP.
To provide market and regulatory samples as per requirement.
Generation, logging, monitoring and closure of TRF as per SOP.
Trending of analytical data for APIs as per SOP.
To provide accurate and adequate data to Marketing Regulatory Affairs department for filing to various regulatory agencies.
Preparation and maintenance of finished product label in system for APIs and perform reconciliation of API FG labels.
Work allotment and planning.
To perform transport validation activity as per SOP.
Handling of market returned materials as per SOP.
