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We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of manufacturing, testing and release activities for SMPA, its partners, contract testing laboratories, and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases.
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Experience working in more than one product area (e.g. solid oral dose, injectables, combination products), and therapeutic area (e.g. oncology, urology, regenerative medicine) within Quality Control a plus.
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Responsible for compliance with regulatory filings and therefore must have experience in a Quality Assurance and/or Quality Control function for marketed pharmaceutical products or clinical trial materials.
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Enhance quality control practices and optimize internal processes by contributing to the preparation, review and approval of standard procedures and electronic systems. Advanced knowledge and use of software applications, including LC chromatographic analyses, statistical applications, and quality management systems (e.g. Veeva.
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Summary of position : Responsible for monitoring quality control/assurance requirements of all preservation preformed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job.
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This is a dual hat position for both the Construction Quality Control Manager and Site Safety & Health Officer (SSHO). We are searching for a proficient Quality Control Manager/Site Safety Health Officer to join our growing construction business line.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Candidate must possess C5ISR Installation, Quality Assurance, or Quality Control experience. Certification ISO Lead Auditor Training a plus Certified Quality Inspector Certification NAVSEA Connector Certification NAVSEA Cableway Certification NAVSEA Fiber Optic QA/Supervisor Training Structural fit-up, welding, pipefitting, and NDT Level II experience/qualification is a plus.
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The Advisor/Technical Lead is responsible for providing technical expertise and leadership to independently contribute to all aspects of analytical development within the Analytical Development and Quality Control group in support of Avid’s drug development program.
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The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished products undergeneral supervision and in accordance with standard operating procedures (SOPs.
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Train and assist quality control inspectors in interpreting technical and quality control requirements in accordance with ASCE, ACI, AISC, ASME, AWS, RCSC, SSPC and other codes for mechanical, plumbing, electrical and instrumentation and contract requirements.
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The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw Materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs.
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In this role, you will perform and evaluate the analytical quality control testing studies to support assay characterization and qualification and Phase 1 manufacturing for cell therapy. Support analytical technology transfer from Research and Process Development to Quality Control.
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Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality.
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Stiamo cercando un Quality Control Engineer da inserire nel Dipartimento Qualità, del nostro stabilimento di Termoli, a riporto del Quality Manager, in supporto del Process Improver e del Customer & Supplier Quality, con forte attitudine alle attività di analisi e controllo conformità del prodotto, processo e sistema di gestione.
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Author and review Quality documents such as SOP, OOS/OOT, CAPA and Change Control originated internally as well as at the vendor sites. The QC Data Manager will also assist in managing quality events (OOS, OOT, Deviation, Change Control, etc.
$112,000 - $140,000Full-timeExpandApply NowActive JobUpdated Today
Title: quality control Company: Advanced Bioscience Laboratories
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