Teva Pharmaceuticals Chemist I in Sunrise, Florida
Date: Mar 13, 2018
Location: Sunrise, Florida, US, 33325
Company: Teva Pharmaceutical Industries Ltd.
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!
Summary: Performs complex testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records.
Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.
Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.
Conducts scheduled preventive maintenance and calibration of equipment (i.e., pH meter, HPLC, dissolution equipment, etc.).
Prepares standard and sample solutions as required by the test methods.
Operates general analytical instruments during routine testing (i.e., HPLC, GC, UV, automatic titrator, IR, AA and TLC).
Performs wet Chemistry tests (i.e., LOD, pH, titration, etc.).
May perform analysis on intermediate and finished products.
Maintains appropriate documentation (records and lab notebooks) as required by SOP’s.
Complies with all current Good Manufacturing Practices (cGMP) current Good Laboratory Practices (cGLP) and safety requirements, laboratory Standard Operating Procedures (SOPs) and Company policies and procedures.
Complies with good housekeeping and safety practices.
Participates in troubleshooting of analytical test methods and laboratory instruments.
Performs peer review of other chemist’s work.
Performs related duties as assigned.
Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
Quality control systems.
Basic math skills, including basic statistics.
Basic Chemistry or related sciences.
FDA compliance standards, regulations and guidelines.
Sample preparation techniques.
Computer applications and programs.
Compliance with DEA and site requirements regarding the handling, use and disposal of controlled substances.
Reading, writing and speaking English.
Reading, understanding and compliance with Company policies and procedures, including safety rules and regulations.
Operating a personal computer.
Accurately performing routine testing procedures, as scheduled.
Accurately and precisely performs testing.
Physical Requirements and Working Conditions:
Incumbents in this class are subject to extended periods of sitting, standing, walking, lifting materials weighing up to 50 pounds, vision to monitor and moderate to loud noise levels. Incumbents may be exposed to or work with toxic materials, toxic gases, electrical hazards, dangerous tools and equipment. Work is performed in laboratory environments. Incumbents must be able to use personal protective equipment, (e.g. respirators, gloves, etc.)
Bachelors degree in Chemistry or related science from an accredited college or university; and a minimum of zero (0) – one (1) years of related laboratory work experience in a pharmaceutical environment; or an equivalent combination of training and experience.
Manufacturing Quality Control
Group Leader Quality Control
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: Fort Lauderdale
Nearest Secondary Market: Miami