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The MPS is a planned production engineering, manufacturing, and shipment schedule, in weekly capacity-constrained sections, that is derived from outputs of the Initial Project Planning Meetings (IPM's) and consistent discussions and coordination with Technical Project Managers (TPM) and Production Project Managers (PPM.
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Our Vaccine Manufacturing is located in Durham, NC. This state-of-the-art facility established in 2004, manufactures our Company lifesaving vaccines in bulk and finished forms. Due to the importance of this facility in our Company Vaccine Manufacturing network, the facility has seen rapid growth in production volumes and new employees over the last several years; currently Durham employs 1,000+ people.
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About This RoleThe Manufacturing Sr Engineer I designs, specifies, installs, commissions and validates new process equipment, provides engineering technical support and troubleshooting for assigned process equipment and a GMP biological manufacturing area such as Cell Culture, Harvest or Purification.
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Electrical Maintenance Engineer| multi-skilled| Maintenance| Mechanical| Electrical| PPMs| Fault Finding| Mechanic| Wiring| 16th| 17th| 18th Edition| Electrician| Manufacturing| Industrial| Plant| Heavy Machinery| Fitter| Electromechanical| Fault-finding| PLC| PPM| Reactive| FMCG| Extrusion| Equipment| Hartlepool| Stockton-on-Tees| Middlesbrough| Seaham| Peterlee| Wingate| Sedgefield| Newton Aycliffe| Spennymoor.
$41,000 - $44,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Keywords: GMP, GLP, GXP, GCP, bioburden, endotoxin, full-process manufacturing, biologics, deviations, junior role, maintenance, calibration, FDA, EMA, biopharmaceuticals, quality assurance, QA.
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Knowledge of bioprocess engineering principles and familiarity with biopharmaceutical manufacturing processes is preferred. Internal Job Title: Associate Director, Process Data Science Position is on-site in Durham, NC About the role: We are seeking a talented and motivated Associate Director, Data Science to join our team and lead the efforts in driving data-driven decisions and optimizing biopharmaceutical manufacturing processes through insightful data analysis and visualization.
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Your Role We are seeking a highly skilled and experienced CSV Engineer to join our team in Durham, NC. Develop and execute validation plans, protocols, and reports for computerized systems and commissioning and qualification documents used in pharmaceutical manufacturing, ensuring compliance with FDA regulations (21 CFR Part 11), GxP, and other relevant guidelines.
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The Manufacturing Technician/Operator will work in the RTP Packaging area, where Lilly autoinjector devices are assembled and packaged. + Knowledge of lean manufacturing principles. + Previous experience with Manufacturing Execution Systems and electronic batch release.
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Examples of experiences include conventional & non-conventional machining, welding & joining, CNC programming, repair & overhaul, and lean manufacturing. Preference will be given to those with prior internship, co-op or military experience in manufacturing/supply chain or engineering.
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The Sr. Manufacturing Associate I/II – Downstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. Purification of cell culture products per manufacturing batch records and in compliance with quality standards, company policies and current regulations.
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If you have a passion for distillation and brewing, and you are ready to contribute to our team's success, we encourage you to apply for this Temp-to-Hire Manufacturing Distillation Operator position.
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FUJIFILM Diosynth Biotechnologies is an industry leading Contract Development and Manufacturing Organization (CDMO) with locations in Teesside, United Kingdom; RTP, North Carolina; Holly Springs, North Carolina; Thousand Oaks, California; Hillerød, Denmark; and College Station, Texas.
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Work closely with cross-functional teams,including Quality Assurance, Manufacturing, IT, and Engineering, to ensure thatvalidation activities are integrated into project timelines and deliverables.
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Basic understanding and application of instrument, equipment, calibration, and maintenance of various parameters in manufacturing, utilities, and laboratory environments within a cGMP Biotechnology / Pharmaceutical manufacturing environment.
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Electrical/Controls/Automation Engineer Location: Durham, North Carolina Job Description: We are seeking an experienced Electrical/Controls/Automation Engineer to take charge of specifying, designing, configuring, testing, supervising, and manufacturing control, electrical, and automation systems.
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manufacturing job Company: Merck Co in Durham, NC
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