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Assist with weighing of raw materials and electronic inventory transactions utilizing MES and/or Oracle, as well as cell culture and filling unit operations for the manufacture of viral vector products in a cGMP environment using proper aseptic technique, good documentation practices, and sound scientific methods.
$67,915 - $87,890 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Prefer hands-on industry experience in cGMP/Biotech/Biopharmaceutical/FDA regulated industries. Proficient in Computer applications and software (Microsoft Excel, Outlook, Word, Access, Project); compliance specific software programs (Agile, Trackwise, LIMS, Master Control, ERP, etc.
$83,300 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Has previous experience in facilities, utilities, or process engineering in highly regulated manufacturing environments, ideally commercial, biopharma cGMP facilities. 8+ years of previous experience in biotech or pharmaceuticals industry working in a cGMP environment.
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The Maintenance Planner is responsible for planning and coordinating activities related to routine / non-routine maintenance activities, supporting and providing technical advice related to Preventative Maintenance/Repair activities of cGMP production equipment, utilities, and instrumentation associated with Manufacturing Operations under limited supervision.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You have 12+ years in the medical device arena; in-vitro diagnostics manufacturing experience or related regulated industry (i.e. cGMP) required. GenMark's ePlex true sample-to-answer system offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care.
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5 or more years work experience in a cGMP regulated environment preferably in biologics manufacturing Prefer experience knowledge working with Single Use Technologies or modular operations. Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The C&Q Engineering Lead (RLT, Carlsbad) has responsibility for executing and managing equipment, facility, utility, process, primary packaging validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory expectations.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Understanding of regulatory compliance with cGMP, GRAS, and HAACP. PCQI certified and familiar with GFSI standards. Maintain SQF, NOP (organic), and NSF DS GMP Certification, ensuring compliance with SQF, NSF, FDA, customer, and other applicable quality and regulatory requirements.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Understand nomenclature for industrial parts and equipment as indicated on Piping and Instrument Drawings (P&IDs) Good understanding and ability to comply with industry standards and cGMP requirements.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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5 or more years of work experience in a cGMP-regulated environment, preferably in biologics manufacturing. The OSUT will employ a ballroom design, and utilize single-use technology, new analytical techniques, and digital manufacturing systems to deliver a best-in-class bioprocess facility.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Implementing improvements in areas such as cGMP training, core competencies, technical skills, safety, and performance management. Experience on demand planning, inventory management, sourcing, purchasing, and delivery performance.
$125,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Strong knowledge of chemical engineering along with cGMP manufacturing focus. Managerial experience in cGMP manufacturing. Enforce cGMP guidelines. Peptide and oligo nucleotide manufacturing experience in upstream and downstream manufacturing (preferred.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Strong understanding of regulatory guidelines (e.g., FDA, cGMP, ISO) related to environmental monitoring and equipment qualification. Bachelor's degree in a relevant scientific discipline (e.g., Biology, Chemistry, Biochemistry) or equivalent work experience.
$48 - $52 an hourExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Under general supervision, this position entails planning and performing calibration tasks in a cGMP manufacturing environment, scheduling repairs for analytical instruments, assist in the coordination and/or oversight of calibration vendors, troubleshooting and repair of malfunctioning instrumentation on solvent systems, utilities systems, and large-scale manufacturing skids, among other tasks.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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May work in the clean room environment that requires gowning in the form of hospital scrubs coveralls gloves and steel toe boots be worn. The OSUT will employ a ballroom design utilize single-use technology new analytical techniques and digital manufacturing systems to deliver a best in class bioprocess facility.
ExpandApply NowActive JobUpdated 6 days ago
cgmp job in Vista, CA
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