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Bachelor's in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 8+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
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RCM is seeking a highly motivated and detail-oriented Technical Support Specialist to join our client's growing team in Branchburg, NJ. This full-time contract position offers a competitive salary of up to $45 per hour and the opportunity to play a vital role in a GMP-regulated pharmaceutical (API) manufacturing environment.
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Nice to have: " Pharmaceutical, lab automation and robotics experiences. Responsibilities " Perform analytical testing in the laboratory using techniques including but not limited to chromatography, spectroscopy, and spectrophotometry.
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Advanced knowledge of pharmaceutical, manufacturing and laboratory systems. Understanding of investigations, deviations and CAPA management in a regulated pharmaceutical industry. Title: Equipment Commissioning & Qualification (ECQ) Engineer/Equipment Validation Engineer.
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Languages: Fluent in English Experience: At least years pharmaceutical manufacturing experience (including a detailed knowledge of BPO Processes, GxP, Compliance Regulations); Comprehensive experience in commissioning and start-up of biopharmaceutical manufacturing plants; Strong customer and supplier relationship management experience; Solid understanding of the overall technical environment of the company; Strong influencing and negotiation skills Good verbal, written and communication skills.
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Location: Madison, New Jersey Type: Contract Job #78837 Our client, a leading pharmaceutical company, is hiring an Administrative Assistant on a contract basis. Knowledge of company systems and processes strongly desired (for example: Concur Travel and T&E, Ariba/SAP, SharePoint, eSetup, Workday, Room scheduler.
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MS in Statistics/Biostatistics and at least 10 years of relevant pharmaceutical experience or a PhD in Statistics/Biostatistics with more than 6 years of' relavant pharmaceutical experience.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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One of our large pharmaceutical clients is looking to hire a Quality Specialist to join the growing External Quality team within Advanced Therapeutics. Minimum 4-6 years of experience working with analytical methods i.e. flow cytometry within QC manufacturing space.
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Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expanding. Minimum of 7 years experience in a GxP role; Pharmaceutical experience is preferred.
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Adecco Medical & Science is hiring a remote contract Regulatory Affairs Specialist Project Lead for our Pharmaceutical partner in Bridgewater, NJ.The anticipated wage for this position is between $88 and $89.22.
$88 - $89.22TemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Candidate Profile:Seasoned professional with 5-10 years in Pharmaceutical Sales or ProcurementIn-depth understanding of APIs/CDMO operations and the US Pharmaceutical Market is highly desirableLocation:Based out of our Bridgewater Office in New Jersey, with the flexibility of partial remote work.
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4 to 7 years of pharmaceutical advertising agency experience. Familiarity with pharmaceutical medical, legal, regulatory (MLR) review process and systems. Partner with internal senior managers, strategy, finance, etc, to ensure optimal client satisfaction, business development, and revenue potential.
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Prior experience in the pharmaceutical industry as a Publications Manager is preferred. 5+ years' relevant pharmaceutical/ biopharmaceutical industry experience. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.
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Experience in the qualification of cell therapy equipment a plus. The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service.
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Minimum 3 years' experience (pharmaceutical/biotech or related agency) Hematology, Oncology or Cell Therapy/Gene Therapy experience strongly preferred. We are an EasyHiring recruiting company that is looking for candidates for our partners for the position of Senior Product Manager, US Marketing- Cell Therapy in Scotch Plains, NJ for work in Princeton, NJ.
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pharmaceutical job in Bernards, NJ
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