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Some technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles Position Reports to Jenna Walker – Associate Director, QA Training & Document Control Education: Bachelor’s degree or equivalent Key Requirements and Technology Experience: Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
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BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. Experience working with SOPs, GDP, GMP, CLIA, and the FDA. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd.
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Position Overview: We are seeking an experienced and dynamic Pharmaceutical Field Sales Representative to join our team, specializing in the sales of sterile injectables listed on the FDA Short List. The successful candidate will play a pivotal role in promoting and selling our range of products, including Lidocaine with and without epinephrine, Ketamine, Bupivacaine with and without epinephrine, and others, to hospital pharmacies.
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That’s how we tackle rare disease. By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s and.
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U.S. based e mployee s may be eligible for s hort -t erm and/or l ong- t erm incentiv e s. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
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Live near a BioLife Plasma Services location or be willing relocate to Appleton, WI for the duration of the program. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
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Comprehensive knowledge of FDA Short List products, including Lidocaine, Ketamine, Bupivacaine, etc. We have an opening for Pharmaceutical Field Sales Representative positions. Develop an in-depth understanding of our sterile injectable products on the FDA Short List.
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As a Microbiologist you will apply cGLP, cGMP, ANSI, AAMI, ISO, EUMDR, FDA and USP guidelines to the bioburden, cytotoxicity, bacterial endotoxin, and biocompatibility analysis of orthopaedic implants and surgical instruments for Leesburg, VA facility.
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Experience representing an FDA regulated company, including knowledge of corporate law, fraud and abuse laws, Anti-Kickback law, Sunshine Law, AdvaMed Code, HIPAA, and other laws and regulations pertaining to the pharmaceutical or medical device industry.
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Relocation: After completing the program and being promoted into a management position, you’ll be required to relocate to one of BioLife’s locations. As a Manager Trainee , you will participate in a training program that will further develop your leadership skills and prepare you for accelerated career growth.
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Must have experience in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes.
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We are a pharmaceutical packaging company looking for someone who is proactive and will to learn and grow. Company Description We are a pharmaceutical packaging company looking for someone who is proactive and will to learn and grow.
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In-depth knowledge of cGMP's, especially FDA regulations CFR Parts with preferred understanding of regulations for computerized systems Strong understanding and operating awareness of working in a pharmaceutical company.
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Fifteen (15) years of experience in Regulatory Affairs and Quality experience in the biotechnology, medical devices, or pharmaceutical industry with increasing responsibility (including interfacing with FDA and other regulatory agencies in development and commercialization of new medical technologies.
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A Minimum of 0-2+ years Biotech/Pharmaceutical experience or equivalent industry experience Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products as well as knowledge of Good Tissue Practices.
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