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Overview Performs any basic to complex Analytical assay(s) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Associate Scientist - QC Manufacturing performs and directs assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs.
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Job Overview: A law firm in Philadelphia, PA, is seeking an experienced Intellectual Property Attorney specializing in synthetic organic chemistry, biochemistry, and pharmaceutical sciences. Drafting and prosecuting patent applications in the fields of synthetic organic chemistry, biochemistry, and pharmaceutical sciences.
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Experience within biotech or pharmaceutical industry strongly preferred, particularly in cell and gene therapy, or ability/interest to learn applicable process technology to provide necessary legal support; and.
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The Clinical Pharmacist Specialist for Abdominal Organ Transplant is responsible for the provision of pharmaceutical care to all abdominal organ transplant (liver, kidney, and pancreas) recipients.
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Minimum five (5) years of experience in in a cGMP Quality Control microbiology role; experience with cell therapy products is a plus. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
$100,000 - $115,000 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The packaging operations team at the Philadelphia facility is responsible for overseeing clinical pharmaceutical packaging operations activities. Oversees primary and secondary packaging areas equipped with various types of pharmaceutical packaging equipment.
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We are currently recruiting a Validation Engineer III who will be part of a growing engineering group supporting all units within the Vector Program in addition to our cGMP manufacturing team. As a Validation Engineer III, under the direction of the Process Engineering Manager, you will be responsible for assisting Vector and GMP personnel with all aspects of the equipment life cycle, including equipment specification, installation, and validation.
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My client who is a leading Global Consulting firm is currently looking to on board an experienced SAP Pre-Sales Architect with a deep background within either Pharmaceutical, BioPharma or MedTech customers.
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You'll be responsible for providing Quality Systems oversight and support for the development and operations of a commercial scale state-of-the-art cGMP cell therapy manufacturing and laboratory facilities.
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We are seeking a highly skilled NextGen/e-Clinical Works Analyst to join our team in advancing our Real-World Evidence (RWE) capabilities within the pharmaceutical industry. Proven experience (3+ years) working with NextGen, e-Clinical Works, or similar electronic health record (EHR) systems in a pharmaceutical or healthcare setting.
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The Worldwide Real Estate and Facilities (WREF) organization oversees and operates 16 million square feet of space with a population of over 28,000 GSK and other staff, including all pharmaceutical R&D laboratories and pilot plant, Consumer Health R&D laboratories and pilot plant and commercial office accommodation for all GSK business units.
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MD, PharmD and/or PhD with 8-12+ years experience or MS with 12-15 years experience in the pharmaceutical industry or healthcare sector, with joint experience / degree in Computer Science, Medical Informatics or Bioinformatics.
$165,200 - $236,000 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Knowledge of and adherence to all PCI, EHS, cGMP, and GCP policies, procedures, rules. These duties include but are not limited to: Installation and drywall repair, Painting, Carpentry, Intermediate plumbing, Intermediate electrical work and installation, HVAC PM's and repairs, Filter changes, Ceiling tile installation and maintenance, assembly of furniture and equipment, Snow and ice removal.
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With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide.
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pharmaceutical cgmp jobs in Philadelphia, PA
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