USV Pvt. Ltd is Hiring for Quality Assurance and has issued notification to accept Applications.USV Private Limited is an Indian multinational pharmaceutical and biotechnology company in Mumbai, India. The company operates across 75 countries globally, and is a leading producer of Metformin in India. The company was founded by Vithal Balkrishna Gandhi to provide affordable and quality healthcare to every Indian. Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Quality Assurance as follows.
Vacancy summary details :
- Company Name: USV Pvt. Ltd
- Location :Manjusar, Vadodara, Gujarat
- Post Name: Quality Assurance
- Qualification: B.pharm/M.pharm
- Experience: 3 to 12 years
- No of Vacancies: Not Disclosed
- Details of Salary: Not Disclosed
- Contact: ajeet.rawat@usv.in
- Closing date for online Application : Apply as soon as possible
- Mode of application : online
- Selection Process: Shortlisted candidates may called for selection process (Â Personal interview , Group discussion , etc…,)
Job Description/Skills Required:Â
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.
Note:If interested candidates can share your resume to mentioned mail ID Below.
