Apr 10, 2018
West Chester, Pennsylvania, US, 19382
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!
We are seeking a highly motivated individual with experience in the area of regulated bioanalytical operation to support pre-clinical (GLP) and clinical regulated studies. The position will focus on document review, SOP preparation, report preparation for method validation, non-clinical and clinical sample analyses of biologics (large molecules). You will be a member of Biologics, Assays and Technology, which plays a critical role in development of biological therapeutics from early stage research, IND enabling GLP studies, clinical trials through BLA submission and post marketing support.
Performs review of documents/records in support of immunogenicity and PK/PD/Biomarker method validation and sample bioanalysis.
Assist in sample tracking and management in Watson LIMS
Assist with documentation, record management, and other laboratory operation activities
Attends regulatory training, SOP training, general laboratory/safety training
Participate in meetings with QA regarding schedules of deliverables
B.S. in a related field with a minimum of 3 years of bioanalytical experience in
B.S. in a related field with a minimum of 3 years of bioanalytical experience in pharmaceutical, biotechnology, and/or CRO industry. Previous experience in data review and report preparation in support of large molecule assays is preferred. Proficiency in Microsoft Office, and knowledge on data integrity and regulatory requirements are expected. Knowledge on Watson LIMS is a plus. The candidate must be able to work collaboratively in a diverse, fast-paced environment with ability to multi-task. Good communication and interpersonal skills are required.
Biologics, bioanalytical assays, SOP and report preparation, Watson LIMS
Research & Development
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.
Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.
Website : http://www.tevapharm-na.com/
Established in Jerusalem in 1901, the company known today as Teva started out as a small business distributing imported medicines throughout the land, using mule trains and camel caravans. The young company was named after its pharmacist founders: Salomon, Levin and Elstein Ltd.