Teva Pharmaceuticals Quality Control Group Manager in Vilnius, Lithuania

Quality Control Group Manager

Date: Dec 6, 2018

Location: Vilnius, LT, 08409

Company: Teva Pharmaceutical Industries Ltd.

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

The role is mainly responsible for quality control compliance to the local laws and regulations as well as standards of the European and United States Pharmacopoeias and the good manufacturing practice (GMP), the analytical methods used are appropriate and validated and that the results obtained are reliable and evaluated according to the specified quality parameters.

KEY RESPONSIBILITIES:

Allocation and coordination of team work

Reviewing and approval of QC work

Ensure that the work is performed according to SOP and timely documented and that results of analyses are correct

Ensure data integrity

Preparing sections on product QC for the annual product review

Guarantee the correctness of product stability tests, quality of API

Validation of methods based on protocols & reports

Preparation and update of SOP

Elimination of laboratory errors and deviations from SOP

Management of analytical cell banks

Reporting accurately & on time

Compliance with internal & external regulations, SOP and laws

Qualifications

University degree in natural sciences (molecular biology, biochemistry, biotechnology, microbiology or chemistry);

2 years+ of managerial experience

Knowledge in analytical assays, preferable but not limited to ELISA, qPCR, Cell based potency assays, Western Blot, SDS-PAGE;

Protein chemistry knowledge;

Previous work experience in pharma industry in laboratory;

GLP & GMP knowledge;

Ability to work on multiple projects and tasks;

Proven ability to effectively collaborate with internal and external parties, in a fast-paced and complex environment;

Strong leadership skills;

Fluent English in writing & reading;

Native Lithuanian;

Strong drive for results;

Exceptional interpersonal skills and good judgment; analytical skills

Flexible, dynamic, highly energetic and very well organized;

Can-do attitude;

Highly proficient PC user

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

QC Manager

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, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

EOE including disability/veteran