| Distance: | Job alert | Jobs 71 - 80 of 33382 |
Senior IP Attorney
NxT Level
–
Seattle, WA, 98127
... Minimum Requirements: Experience representing biotechs and big pharmas as they license patents and collaborate to advance novel therapeutics, vaccines, diagnostic and digital health technologies through clinical trials and toward regulatory (FDA) ... - Dec 03
Sr Mechanical/Process Design Engineer/Technical Lead (Pharma/cGMP/FDA
Jobot
–
Philadelphia, PA
... will have 8-10 years of experience with an Engineering Consulting Firm performing Mechanical and Process/Piping Systems Design for Cleanrooms, Laboratories, FDA-Regulated Environments, Pharmaceutical Manufacturing Facilities, and cGMP Facilities. ... - Dec 05
Quality Assurance Specialist II
PolyPeptide US
–
Torrance, CA, 90504
... Strong understanding of FDA, ICH, and EU regulatory requirements. Experience with batch record review, investigations, and CAPA systems. Excellent communication, organization, and problem-solving skills. Proficiency with Microsoft Office and ... - Dec 03
Post Market Quality Engineer
Hologic
–
Marlborough, MA, 01752
... Participate in internal and external audits, including FDA inspections and supplier audits. Support monthly Quality Investigation Review boards. Qualifications & Experience: Bachelor's degree in Mechanical, Biomedical, Biomechanical, or Electrical ... - Dec 03
Quality Compliance Specialist
Glenmark Pharmaceuticals USA
–
Monroe, NC, 28111
... Knowledge and Skills : Strong understanding of current GMPs and related regulatory health authority guidance (FDA regulations, ICH guidelines, etc.) as they relate to the pharmaceutical industry. Must be proactive, results-oriented with a strong ... - Dec 03
Formulations Scientist - Gummies
International Staff Consulting
–
Lexington, KY, 40598
... ingredients, etc) and previous experience in scale-up/commercialization work Previous experience in GMP and/or FDA manufacturing and lab environments is a must-have Should be able to demonstrate a track record of attention to detail in previous work - Dec 03
Clinical Research Gastro enterologist (part-time) - San Antonio, TX
Protouch Staffing
–
Fair Oaks Ranch, TX
... Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards. Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution. Document patient interactions, ... - Dec 03
R&D Lab Technician
Nice-Pak
–
Woodcliff Lake, NJ, 07677
... Willing to learn EPA, FDA, ICH, etc. regulations related to their testing. Read and comprehend Company policies and procedures, including safety rules and regulations. EXPERIENCE REQUIRED 0-3 years of experience in an R&D or QC lab, or an equivalent ... - Dec 03
Pr. Technical Writer, Labeling
Inspire Medical Systems
–
Sarpin, Samsun, 55400, Turkey
... 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. Inspire Medical Systems is committed to enhancing patients' lives ... - Dec 03
TMF Specialist
Allen Spolden
–
Savannah, GA
... pharmaceutical/biotechnology or CRO organization in TMF management Working knowledge of VEEVA Vault Strong working knowledge of FDA & ICH/GCP regulations and guidelines and thorough knowledge of clinical monitoring procedures Proficient in computer ... - Dec 03