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!
Teva is searching for a QC Analyst (Raw materials) to join our team in Cincinnati, OH!
The QC Analyst actively participates as a team member supporting the routine and non-routine testing of drug substances and raw materials in the QC Laboratory.
You will perform analytical bench chemistry according to established compendia and vendor specifications, and have strong problem solving, method validation, cleaning validation and analytical capabilities. You must be able to work independently to achieve team goals and milestones.
Perform analyses and tests of raw materials, packaging materials, quantitative assays on samples, and/or internal reference standard qualifications, to ensure quality standards and compliance with established specifications
Perform a variety of qualitative tests or qualitative assays on samples using techniques that vary from standard analytical equipment to modern and automated instrumentation.
Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data
Be responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation
Come from a broader understanding of other aspects of the business and apply quality principles when reviewing documentation and making decisions/ suggestions
Stay current on new requirements & making associated recommendations that affect area of expertise
Apply root cause problem solving principles for identification and implementation of effective corrective and preventive actions
Use risk assessment tools within own area using knowledge, managing risk and assessing impact to make decisions
Promote Quality and GMP by analyzing the implications of deviations, and implement solutions under guidance.
Serve as a mentor for more junior analysts within the team providing guidance and direction as needed
BS or higher in science related discipline required. Chemistry is preferred
Minimum 5 years of experience in a pharmaceutical environment required
Advanced knowledge of analytical chemistry and chromatography (GC/ HPLC/ UHPLC) required
Ability to write technical documents (i.e. protocols, reports, change controls, SOPs) required
Thorough knowledge and understanding of USP, cGMP, ICH and FDA guidelines required
Manufacturing Quality Control
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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.
Nearest Major Market: Cincinnati
Teva Pharmaceutical Industries