Teva Pharmaceuticals Quality
Specialist
Date: Dec 4, 2019
Location: Gwalior, IN, 477117
Company: Teva Pharmaceuticals
Company Info
Teva is a global pharmaceutical
leader and the world's largest generic medicines producer, committed to
improving health and increasing access to quality health solutions worldwide.
Our employees are at the core of our success, with colleagues in over 80
countries delivering the world's largest medicine cabinet to 200 million people
every day. We offer a uniquely diverse portfolio of products and solutions for
patients and we've built a promising pipeline centered around our core
therapeutic areas. We are continually
developing patient-centric solutions and significantly growing both our generic
and specialty medicines business through investment in research and
development, marketing, business development and innovation. This is how we
improve health and enable people to live better, healthier lives. Join us on
our journey of growth!
Job Description
Review and approval of executed /
master batch cards and other production related data.
Control, distribution & Archival
of all documents.
Responsible for coordination and
supervising dispatch and related activities.
Responsible for initiation, review of
change controls system related to process, monograph, facility, SOP’s, vendor
etc.
Coordinating for investigating, review
and closing of deviation, OOS, OOT, CAPA and related task. Follow up and
implementation CAPA with effectiveness verification.
Coordination and review of
Qualification/Validation documents and engineering files and related task.
Carrying out quality system audits /
internal audit to verify compliance with principles of quality system GMP /
GLP.
Coordination, review and archival of
technology transfer documents. Review and update of time limitation and process
parameters.
Coordination in stability sample
initiation for validation batches, annual batch and others.
Review and verification of documents
and updation in computerized system.
Filling of Customer Questionnaires
and other customer related Queries.
Responsible for preparation and
review of annual product review.
To perform the risk assessment.
Batch card auditing & retrieval.
Qualifications MSc - Chemistryn2 to 4
Yrs of Exp.
Function Quality
Sub FunctionnManufacturing Quality
Assurance
Reports To In process of validation
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