Teva Pharmaceuticals Hiring for Documentation Specialist -II at Gwalior Full Time

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

• Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines
• Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team
• Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision
• Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives.
• Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment
• Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills
• Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR)
• Coordination of production tasks to meet assigned schedule

Qualifications

B.Tech Chemical /BSc -Chemistry// Diploma
2+ years expreince in API Production

Function

Sub Function

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Teva’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.