| Job alert | Jobs 61 - 70 of 475 |
Clinical Development Director - Hepatology
GlaxoSmithKline
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Collegeville, PA, 19426
... Knowledge of ICH guidelines, FDA requirements, regulatory and reimbursement data requirements in responsible area Experience with needs and priorities of regulators, payers, and prescribers in relevant market(s) Experience using new learning and ... - May 21
Senior Project Manager - Remote
ClinChoice Inc
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Whitemarsh Township, PA, 19034
... • Knowledge of FDA regulations, drug development and PM processes. • Good understanding of ICH/GCP guidelines. • Strong presentations skills. • Strong communication skills, both oral and written. • Strong team player, interpersonal skills, and ... - May 24
Site Mechanical & HVAC Engineer
Spark Therapeutics
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University City, PA, 19104
... Experience with FDA, USP, ICH, EMA, ISPE. Demonstrated ability to lead investigations, study execution, and produce high quality technical documentation. Proven track record in a CAPEX program environment. Spark takes into consideration a ... - May 11
Vice President, Director, Regulatory Review
Publicis Groupe
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Philadelphia, PA
... Web: Facebook: Twitter: Job Description Within Digitas Health, the Vice President, Director, Regulatory Review will provide advice to creative, strategy, planning, marketing, and other capabilities on the latest updates from FDA and other regulatory ... - May 28
Sales Support Associate
Globus Medical, Inc.
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Audubon, PA, 19407
... Accounting, and Product Development Management as necessary Follows all procedures outlined in Globus Medical’s Quality Policy and Employee Handbook to ensure total conformity with the FDA and other government agencies Assists Shipping Dept. ... - May 29
Clinical Trainer (Philadelphia, PA)
Inspire Medical Systems I
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Philadelphia, PA, 19019
... We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Our focus on patient outcomes is at the core of everything we do, and ... - May 26
Digital Quality Manager R&D US
CSL Behring
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King of Prussia, PA, 19406
... Knowledge of GxP, GAMP, FDA, and EMA requirements specifically CFR21 part11 and Annex 11. Work with important partners at all levels of the company. The expected base salary range for this position at hiring is $95,000- $130,000. Please note this ... - Jun 01
Lead for Global Regulatory Affairs, Plasma
BioSpace, Inc.
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King of Prussia, PA, 19406
... You will lead and direct strategy for regulatory compliance for all CSL Plasma Inc Operations to include: o Authorized Official contact e.g., with FDA and other health authorities. o Serve as a liaison/representative for our submission to regulatory ... - Jun 03
Manager/ Sr. Manager Medical and Scientific Writer
Ocugen, Inc.
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Malvern, PA, 19355
. Target Bonus and Equity
... Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting them to FDA. Conduct quality control and editorial review of documents prepared by team ... - May 16
Production Technician - Clean Room
Ecolab
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King of Prussia, PA, 19406
... Knowledge of FDA requirements Title 21 part 210 & 211 in Manufacturing, Processing, Packing, or Holding of Drugs and Finished Pharmaceuticals. Will be responsible for of ensuring quality, productivity, and operating equipment in the clean rooms. ... - Jun 01