Sun Pharma Released Great Job Offer For B.Pharma,M.Pharma,B.Sc,M.Sc

Sun Pharmaceutical is hiring for Sr. Manager QA . Sun Pharma beginnings in 1983, Sun Pharma has grown to become the 5th largest generic pharmaceutical company in the world and No. 1 in India. Application form link provided at the end of post.

Vacancy Details :

• Company Name: Sun Pharmaceutical
• Location : Ankleshwar
• Post Name: Sr. Manager QA
• Qualification: B.Pharma,M.Pharma,B.Sc,M.Sc
• Experience: 15 – 20 years
• No of Vacancies: 01
• Details of Salary:  NA
• Mode of application : Online
• Selection Process: Personal interview
  

Job Description/Skills Required :

• Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site.
• Responsible for defining operational strategy and road map for quality assurance management at site.
• Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements.
• Responsible for efficient use of human resources and adequate staffing of all areas with capable trained personnel aligned to Operations and departmental objectives. Performance measures are utilized to ensure that departmental activities are effective and timely and as the basis for continuous improvement. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year.
• Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site.
• Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle.
• Review and approve the documents as per quality procedures.
• Review/support to draft response of internal/external audit observations for computerized systems and ensure its compliance.
• Ensure site GxP computerized systems assessment are performed for ensuring 21 CFR part 11 and EU Annex 11 readiness and adequate security and controls to ensure data security.
• Provide support in remediation of the gaps identified during site GxP computerized system assessment in a timely manner.
• Represent the identified quality exposures/ risks of computerized systems in the QRB meetings.
• Ensure the QMS (Deviations, Change Control, CAPA, incidences etc.) related to computerized systems are closed in timely manner
• Work in partnership with the site cross functions and corporate functions for implementation of new initiatives for computerized systems.

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply