USV Pvt Ltd Job Vacancy For IPQA/ QMS/ Documentation/ Validations - QA

USV Pvt Ltd Job Vacancy For IPQA/ QMS/ Documentation/ Validations - QA 

USV Pvt Ltd Job Vacancy For IPQA/ QMS/ Documentation/ Validations - QA 

USV Private Limited– A leading Pharmaceuticals Company is hiring for its new state-of-the-art formulations manufacturing facilities at Vadodara. The location of the plant is at Savli-Manjusar, Vadodara, Gujarat. Come & Join an exciting journey of Growth and Development

We required following personnel for QA function, Qualification required B.Pharm/M.Pharm

IPQA – Officer/Sr. Executive (Exp – 3-7 yrs.) Responsible for in process checks, Batch execution document review, AQL, shop floor investigation & Sampling of regular batches as well as validation batches at various stage of Manufacturing & Packing. Candidate should have good knowledge about GMP guidelines. Candidate having exposure or knowledge about MES or any other electronic system for manufacturing execution will be preferred.

IPQA- Section Head – Asst. Manager/ Dy. Manager (Exp. 9 – 12 yrs.) Require good knowledge of QMS/CAPA. The candidate must possess good Investigation, Problem solving & troubleshooting skills. Candidate having exposure or knowledge about MES or any other electronic system for manufacturing execution will be preferred.

QMS – Executive/ Asst. Manager (Exp. 5-8 yrs) Person independently handling the QMS activities and involved in the investigation of all events like Market Complaints, Deviation & CAPA, Product recall and trend evaluation of QMS events. He should have good knowledge of master documents and must possess communication skill..

QMS (Investigations) – Executive/ Asst. Manager (5-8 yrs) – Responsible for QMS events investigation i.e. Deviation/ Complaint/ Recall/ OOS/OOT/Incident. He must be well versed with investigation tools. A person having good knowledge of regulatory norms. He also need to possess good communication skills.

Validation / Qualification – Executive/Asst. Manager (Exp. 5-8 yrs) – Responsibility involves conducting all type of validation/qualification activities in the plant (both process & utilities). The candidate should have good knowledge of GMP guidelines & regulatory requirement. Must possess sound problem solving/ troubleshooting skills.

Documentation – Officer/Executive (3-6 yrs Exp) – Responsible for documents preparation / issuance/ retrievals. Also responsible for master formula records. A person having good knowledge regulatory expectation. He must possess good communication and presentation skills.

Share your CV at ajeet.rawat@usv.in