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Zydus lifesciences Ltd Urgent recruitment for QA professional for our OSD Manufacturing Facility -Salary:₹ 8-12 Lacs P.A.

SWARNALATHA B September 2, 2023

Zydus lifesciences Ltd Walk In Interview 2023 . zydus lifesciences Ltd Notification full details below.zydus lifesciences Ltd (also known as Zydus Cadila) is an Indian multinational pharmaceutical company headquartered in Ahmedabad, Gujarat, India primarily engaged in the manufacture of generic drugs. It ranked 100th in the Fortune India 500 list in 2020. Cadila was founded in 1952 by Ramanbhai Patel (19252001), formerly a lecturer in the L.M. College of Pharmacy, and his business partner Indravadan Modi. 

Vacancy details:

  • Department:  QA professional for our OSD Manufacturing Facility
  • Qualification: M.Pharmacy/ B. Pharmacy
  • Experienced:8-12 Years of experience in Qualification and Validation.
  • Salary:₹ 8-12 Lacs P.A.

Job Description: Greetings from zydus lifesciences Ltd   !!!!

Important Details :

  • Location: Ahmedabad, Gujarat, India
  • Salary:  Not Disclosed by Recruiter
  • Post of date:02/09/2023
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face to face
  • Interview Rounds of Interview: HR

We are looking for QA professional for our OSD Manufacturing Facility based out of Ahmedabad. Please find the details below

Roles and Responsibilities :

To prepare, review and implement Standard Operating Procedures.

Issuance and retrieval of documents.

To prepare/review and impart training on various procedures and to ensure effective implementation of training program.

To prepare, execute and review of equipment/ instrument/ system /utility /area qualification program.

To prepare, review and implement Standard Operating Procedures.

To review computerized system validation documents.

Preparation & review of cleaning validation assessment, protocol & report.

To Initiate, review and investigate deviations, out of trend/out of specification results.

To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness.

To initiate & review change controls and to monitor change control execution for timely closure.

Prepare and execute Internal Audit program.

To prepare & review risk assessment documents.

To prepare and periodically review Validation Master Plan, Site Master File.

Candidate details:

The candidate should be from Pharma(OSD) Industry only.

The candidate should Have knowledge and Exposure of GDP/ GMP.

The candidate should have good communication skills (Verbal & Written)

The candidate should have Regulatory exposure(USFDA).

Interested candidate, Please share the resumes at my mail id manan.hathi@zyduslife.com.

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