Home / Job / USV Private Limited – Multiple Openings for Quality Assurance Department

USV Private Limited – Multiple Openings for Quality Assurance Department

USV Private Limited – Multiple Openings for Quality Assurance Department

USV Pvt Ltd Jobs 2021 Vacancy for Experienced at Mumbai Apply Now

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 [email protected]

Date of Posting: Jul 28, 2021

http://www.usvindia.com

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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