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Supervise and ensure compliance with ISO/GMP/FDA/class 7 requirements. The Lead will maintain a skilled manufacturing team of no more than 5 employees responsible for filling, assembly, and formulations to ensure production of high-quality products.
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Facilitated training and development programs designed to increase knowledge in issues related to medical device development, such as GMP, Quality Systems, etc., as well as their application at.
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Two-year Vo-Tech Certificate in electronics or related technical field and seven or more years progressive experience as an engineering technician in a electrical engineering or testing organization; High School diploma or equivalent and twelve years progressive experience as an engineering technician in a related position within a manufacturing or testing organization also meets minimum requirements.
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Certified IPC specialist (CIS) that meets the IPC-A610 Standard for Acceptance Criteria for Printed Circuit Board Assemblies preferred. To qualify for internal promotion, the most recent annual performance appraisal as an Engineering Technician III must be at "Exceeds Position Requirements " level, or above.
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Leads and manages department staff and processes to support manufacturing of dietary supplement products in a GMP manufacturing environment. Amerilab Technologies is a growing and leading US manufacturer in the development, manufacturing, and packaging of effervescent tablets, and effervescent and non-effervescent powders in stick packs and sachets, and we are currently seeking skilled and experienced Engineering Manager to join our team.
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Project management, Project engineering, GMP, capital project, facilities design/layout, facilities maintenance/management, medical device. Best candidate will have a background in pharmaceutical manufacturing.
ExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Preferred at least 3 - 5 years of applicable experience in GMP pharmaceutical manufacturing environment or equivalent experience. Report daily progress to Manufacturing Management.
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Compliance with all GMP, HAACP, Food Safety, Food Defense, and SQF policies and procedures. Wear appropriate personal protection equipment and adhere to dress code as outlined for working in a food manufacturing facility.
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Expected to adhere to safe work practices, follow GMP and HACCP guidelines, maintain sanitary conditions and ensure that product quality is maintained in order to maintain SQF certification. Must follow all Good Manufacturing Practices (GMP’s), Hazard Analysis and Critical Control Points (HACCP) and Safety regulations for the area with the ability to learn and understand cross contamination issues and how to avoid them.
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We are seeking an Entry-Level Documentation Specialist to join their team in Irvine, CA. As a Documentation Specialist, you will play a vital role in ensuring the smooth operation of our manufacturing processes by meticulously creating, processing, and reviewing production batch records in accordance with established GDP/GMP procedures.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Required basic knowledge of manufacturing processes: key focus into metrology, precision machining, grinding, product cleaning, and sterilization. Assuring compliance to internal or external specifications and standards (i.e. GMP, ISO, FDA, CMDR.
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Follow all Standard Operating Procedures (SOP), Good Manufacturing Practices (GMP), Standard Work (SW) to produce restorative dental products while maintaining machines at maximum production levels and adhering to safety standards.
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Perform routine ICP-MS and ICP-OES analysis for trace metals in a GMP analytical laboratory. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required.
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Enforce Kerry manufacturing standards in the areas of ingredient and product standards, process specifications, formula compliance, sanitation/GMP/pest control, and regulatory audit compliance.
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Comply with all standard safety practices, safety rules, GMP and all CCNA rules and policies. Receive, store and distribute raw materials, packaging supplies and finished goods common to the beverage manufacturing process.
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