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!
Under supervision, performs analytical testing of finished dosage pharmaceutical products and/or performs data audits of standards, reagents, analytical instrumentation and laboratory analyses.
ESSENTIAL AREAS OF RESPONSIBILITY
Perform/audit analytical testing of finished dosage pharmaceutical products and raw materials following analytical methodology.
Read and interpret analytical methodology and the USP.
Follow cGMP and cGLP requirements.
Assist in ensuring testing/auditing is in adherence to schedules through team oriented process.
Maintain accurate, detailed records of work performed using LIMS or other data collection.
Operator basic analytical instrumentation.
Follows TEVA Safety, Health, and Environmental policies and procedures.
Performs other duties as assigned or as business needs require.
Work with team to meet production, validation, stability and request deadlines.
Ensure that finished dosage pharmaceutical products and raw materials are accurately analyzed following analytical methodology, and USP and cGLP requirements.
Laboratory documentation of standards, reagents, and other analytical instrumentation is verified to be accurate.
B.S. in Chemistry or related science
Analytical laboratory experience preferred.
Introductory knowledge of HPLC, GC or other spectroscopic methods.
Introductory knowledge cGMP and cGLP requirements in a pharmaceutical quality control laboratory.
Good computer skills including MS Office.
Ability to perform/audit routine analysis of finished dosage pharmaceutical products and raw materials.
Ability to accurately perform and meticulously document work.
Good organization skills and attention to detail.
Good interpersonal, oral, and written communication skills.
Ability to multitask, handle multiple projects at one time, and change priorities based on business needs.
Able to work effectively independently and as part of a team.
Able to work overtime, including weekends, when required.
May be required to lift/move up to 50 lbs.
Individual may be required to handle hazardous and non-hazardous materials.
Individual may be required at times to wear Personal Protection Equipment.
Not allergic to chemicals or biosubstances found in laboratory or production facilities.
Manufacturing Quality Control
In process of validation
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.
Nearest Major Market: Lynchburg
Nearest Secondary Market: Virginia
Teva Pharmaceutical Industries