Teva Quality Analyst Job Opening - B Pharma & M Pharma Apply

Teva M Pharma & B Pharma Apply – Quality Analyst Job 

Teva announces job opening for pharma candidates. Quality analyst job opening. Quality Analyst vacancy at Teva. Candidates having bachelor’s and master’s degree in pharma may apply for the job vacancy at Teva for the post of quality analyst. B Pharma job, M Pharma job 2022. Intrested and eligible candidates may check out all the details on the same below:

Job Title: Quality Analyst I

Location: Bangalore, IN, 560052

Eligibility Criteria:

  • B.Pharm/M Pharm or MSc in life sciences with Analytical skills,
  • 2-3 experience in QMS, GCP quality assurance audits, and knowledge on ICH-GCP and US and EU regulations and applicable GxP standards/Regulations.

Job Description

• Plan, conduct, and mange Internal audits (Study In process & Retrospective, System Audit) and Vendor audits as per the plan in compliance with SOPs, ICH-GCP, Protocol, and applicable GxP standards/ regulations.

• Preparation of audit reports for the audits conducted and release the audit report to auditee.

• Aid in continuous improvement of quality management system. Assist seniors in team in maintaining all QA correspondence.

• Preparation/Review of SOPs.

• Assess suitability of responses to audit findings and negotiate suitable actions needed to satisfactorily resolve audit findings.

• Review of deviations and CAPA plans and follow-up CAPA plans and ensure for its implementation and closer.

• Assist in preparation of the facility for client/sponsor audits and regulatory inspection

• Perform the reconciliation of Project and Non-project related documents and send for archival

• Review the equipment calibration/validation records

• To perform QA activities in other departments on a need basis and assist QA staff as and when required.

• Review of clinical development document and data management for internal consistency.

• Preparation of standard operating procedures related to the Clinical development and data management quality assurance department.

• Conducting site audit, facility, and quality system audits

• Review of edit check plan and edit check software program (User acceptance testing).

• Review the validated clinical trial data to ensure consistency, integrity, and accuracy based on the project-specific requirements.

• Review of database design and medical coding.

Apply Online

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