Quality Control Analyst II at Teva Pharmaceutical Industries Ltd. - Israel

, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

05 Feb, 26

Salary

0.0

Posted On

07 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Stability Analysis, Method Transfer, Method Validation, Analytical Documents Review, SOP Preparation, Data Management, Calibration, Validation Protocols, LIMS, SAP, LSCMS Software, Quality Forms Initiation, CAPA Management, Training, Technical Documentation, Compliance

Industry

Pharmaceutical Manufacturing

Description

Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.How you’ll spend your day • Detailed description of MAIN tasks and responsibilities: • Performing Stability analysis, Method transfer, Method Validation and review of analytical documents.• Preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of all logbooks of the department• Preparation of departmental SOP’s in compliance with current guidelines. Review of departmental SOP’s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.• Preparation and review of validation protocols in compliance with current guidelines.• Calibration and validation of all instruments / equipments. • Entry of stability sample results in LIMS & SAP.• Handling of LSCMS software• Initiation of Quality Forms in Track wise Harmony, documents in Glorya EDMS and CAPA in Trackwise Harmony.Your experience and qualifications • M. Pharmacy• 10 years and 7 months of experienceTeva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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Responsibilities

The Quality Control Analyst II will perform stability analysis, method transfer, and method validation, along with reviewing analytical documents. They will also prepare and review various protocols and reports in compliance with current guidelines.