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In this role, you will provide air quality consulting services for a broad range of industrial clients throughout the Northeast and Southeast regions of the US. This is a great opportunity to work on challenging projects for chemical, oil & gas, electrical utility, high-tech, food and manufacturing companies.
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With roots dating back over 125 years, we are part of an operation that owns and leases a diversified portfolio of approximately 120,000 tank cars and 10,000 freight cars, operates two tank car manufacturing facilities, and has a network of more than 110 full-service and mini / mobile repair shops.
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Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry with at least 4 years of relevant experience including biological/pharmaceutical research, manufacturing, testing or a related field OR.
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Learns and adheres to Good Documentation Practices (GDP), current Good Manufacturing Practices (cGMP), and CSM's Standard Operating Procedures (SOPs) 1 year of experience with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), or Good Documentation Practices (GDP.
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Biopeptek Pharmaceuticals is a leading Contract Development and Manufacturing Organization (CDMO) specializing in peptide therapeutics. Collaborate with cross-functional teams including process development, analytical, and manufacturing to ensure smooth project progression.
$175,000 a yearExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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ESFM's clients include many household names from Life Science, Technology, Oil & Gas and Manufacturing markets. In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA.
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Our manufacturing client based in the King of Prussia, PA area is seeking an Accounting Supervisor with 5+ years of experience to join their growing team on a contract-to-hire basis. Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement.
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On site we have our state-of-the-art laboratory, clinical, and commercial manufacturing plant for oral dose forms in addition to being the Catalent Center of Excellence for handling Highly Potent Active Pharmaceutical Ingredients.
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Support GMP mammalian and microbial cell banking programs internally and at Contract Manufacturing Organizations (CMO), striving for right first time. Responsible for GMP documentation management including process transfer documents (PTDs), master batch records (MBRs), media forms, standard operating procedures (SOPs), work instructions (WIs), and reports etc.
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Familiarity with protein purification process operations and Good Manufacturing Practices (GMP) regulations. Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field with 1+ years of direct purification experience in a Pilot Plant or manufacturing setting.
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Candidate should have at least 3-5 years of Plant Maintenance/Reliability Engineering experience within high volume and/or industrial manufacturing environments. Candidate should have at least 3-5 years of Plant Maintenance/Reliability Engineering experience within high volume and/or industrial manufacturing environments.
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This is a hands-on role where the Principal Quality Engineer will apply diversified knowledge of Engineering, Risk Management, Supplier Management, and Quality principles and practices for the manufacturing of implantable tissue and medical devices as well as the related surgical tools.
$166,224 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Skills: SOP, Biology, Chemistry, Protein Purification, GMP (Good Manufacturing Practice) Completing daily manufacturing tasks per standard operating procedures and batch document instructions.
$27.79 an hourFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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This experienced Operating Engineer works within a maintenance team that ensures compliant, accurate, and timely completion of corrective, emergency and preventive maintenance in support of biologics pharmaceutical manufacturing and research and development operation equipment.
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Catalent in Somerset, NJ is home to oral solid dose manufacturing operations as part of the Oral and Specialty Delivery (OSD) business unit. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.
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manufacturing job in Broomall, PA
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