Group Leader Maint/Engineering - 6944

Date: Mar 25, 2023



Location: Goa, India, 403722



Company: Teva Pharmaceuticals



Job Id: 46755

Who are we?

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!

• Manager Engineering Compliance & Documentation Lead is responsible for managing and leading Quality Assurance Engineering oversight for Equipment Qualification program for new and existing facilities within Goa Operations.
• Responsible for overall QAE oversight includes but not limited to, all the brown field (new) expansion projects, capacity expansion of existing facilities and support facilities such as New manufacturing & packing Lines ,new Equipment\xe2\x80\x99s, New laboratory system - which should comply with Teva Quality Requirement ,global regulatory requirements, industry best practices and will withstand regulatory inspections.
• As a Manager Engineering Compliance & Documentation Lead, this role is expected to managing people, providing quality & technical direction to Site Engineering Team members, Lead as a Quality Assurance Engineering expert for dept. & face for Site Engineering to cross functional teams.
• Demonstrate active participation in driving and developing strategies for continuous improvement
• Lead Harmonization of the manufacturing equipment, systems, facilities & utilities qualification program and shall provide independent QA oversight for these activities.
• Effectively collaborate with all levels of internal customers within Quality, Safety, Production, QC, Supply Chain, MS&T,CFTs for Quality assurance , Equipment Qualification Validation, Facilities QA compliance , Engineering, Manufacturing.
• This role will assist Site Engineering Head for engineering Compliance & QMS Governance for department.

Qualifications

Bachelor\xe2\x80\x99s degree in Engineering with 08+ years/ bachelor\xe2\x80\x99s degree in Pharma/Lifesciences /FMCG experience in documentation/compliance .Additionally Advance Diploma /PG in critical system such as Water ,HVAC, Air is preferable .

Function

Engineering

Sub Function

Equipment Maintenance Technical Specialty

Reports To

In process of validation

Already Working @TEVA?

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Teva\xe2\x80\x99s 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.