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Pharmaceutical company in need of Director or Senior Director to join the Medical Affairs team. The Medical Director will provide support and expertise in the area of psychiatry either Schizo or Addiction as there are two needs In this newly created and high profile role you will serve as the medical affairs strategic lead for our combination oral schizophrenia treatment that is currently in phase 3 clinical development. The Medical Director is expected to establish key medical strategies for....

- Menlo Park, CA

Education and Qualifications - Pharm.D., PhD, or M.D. or equivalent education. - Preferable five to seven years clinical or clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry. - Participated in clinical oncology studies. Overview The Medical Director will collaborate with company management, design, plan and develop clinical evaluation research studies in hematology oncology. He / She will prepare, author and maintain....


Our client is a world-wide manufacturer and distributor of analytical instrumentation sold into R&D Laboratories. They are creating a new position for a Key Account Manager who will focus on the development of sales and major accounts in the Pharmaceutical and Cosmetics industries for North, Central and South Americas. We are not looking for candidates who were Pharma Sales Reps; we are seeking technical degreed (Engineering, Chemistry, Physics, etc.) sales professional who has sold or....

- Richmond, VA

Multi-discipline engineering consulting firm seeks Sr Process Engineer with responsibility as Project Manager to support manufacturing facilities and clients in the Eastern US. Work with Fortune 500 clients including industries such as food processing, films, fibers, plastics, paper, chemicals, tobacco, pharmaceuticals, metals, and discrete manufacturing. Responsibilities: --- Act as the Face of the organization through effective communication to the Client --- Manage the entire design process


Multi-discipline engineering consulting firm seeks Sr Electrical Designer with responsibility for performing electrical design on assigned projects including power distribution, machine control design, and instrument and control design to support manufacturing facilities and clients in the Eastern US. Work with Fortune 500 clients including industries such as food processing, films, fibers, plastics, paper, chemicals, tobacco, pharmaceuticals, metals, and discrete manufacturing.....

- Middletown, NY

Experience: B.S. Chemical or Environmental Engineering or any Science degree with 3+ years of experience out of a chemical facility. Ideally, this person should have experience out of a PSM regulated site and have experience with all aspects of EH&S. Pluses would be knowledge of the following regulations: air, water, solid waste, industrial hygiene, PSM, and operator safety. This role requires up to 50% travel to plants throughout the US, as well as support to the local NY plant. Job....

- Baton Rouge, LA

Experience: B.S. Chemical Engineering degree with 3+ years of experience out of any PSM regulated chemical plant. This person could have previous chemical process engineer experience with exposure to PSM, have lead or been a part of PSM/HAZOP reviews, or have a strong process calculations background with PSM experience. Pluses would be experience with PHA Facilitation, API, NFPA, ASME, or Root Cause Analysis. Job Description: Our client is a rapidly expanding chemical company that working....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. They have an opening for a Field Service Engineer to be based in the Chicago area or Milwaukee. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Chicago area but will also conduct....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they have opening for a Field Service Engineer to be based in the Kansas City, St. Louis or Springfield. This position may also conduct supplemental travel into other territories on a regular basis.Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in R&D Labs in the assigned....


Here's another outstanding opportunity with a national expanding food/beverage manufacturing company! Apply for immediate consideration! Maintenance Supervisor - Day Shift - $60-72,000 plus 10% bonus - Springfield, MO -- Relocation paid -- Food or Beverage or Rx product manufacturing experience. Rotating shift: · Hours 6am-6pm 3-2-2-3 rotational schedule, with a 3 day weekend every other week. Requirements for the Maintenance Supervisor - Food or Beverage manufacturing experience: - 4 year....


The Quality Assurance Generalist I (QAG I) reports to the Quality Assurance Supervisor. This position is responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QAG I will be readily available to support the production process; therefore, this position requires that the associate stays on the production floor for the majority of the work....


Summary of the Position: The Batch Record Reviewer is responsible for the review and release of batch records, Certificates of Analysis and other pertinent document and relaying this information to the appropriate departments. Roles and Responsibilities:Communicating accurate and up-to-date status reviews to appropriate personnel and updating the Finished Product Release spreadsheet. Additionally on a daily basis, the Batch Record Reviewer will assist in the correction of deficiencies found....

- Lancaster, SC

We are looking for a Quality Control Chemist to work in a cGMP laboratory who will operate laboratory instrumentation, troubleshoot and generate/revise SOPs and test methods.The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation....


Sr. Packaging Automation EngineerServe as the technical lead on Software Change Requests (SCR’s) and Automation projects for site Packaging areas as well as the Waste Water and Powerhouse areas. Responsible for assisting users in capturing their desired requirements, translating these into implementable Automation solutions, and delivering these on a timely basis.Leverage a deep understanding of Allen-Bradley PLC/HMI platforms to maintain and enhance existing machine control code. Leverage....


We are seeking an experienced Project Engineer with strong consumer product packaging, capital equipment installation, and continuous improvement experience within a food manufacturing plant environment. This role will support a local production facility in Minnesota and also provide project management and technical support for several other plants within the U.S. Strong engineering, problem-solving, Lean, Six Sigma, and capital equipment startup/commissioning experience is desired. Prior....


Position Overview The Director Real World Evidence Analytics ensures that real-world evidence (RWE) studies and queries are strategically designed and optimally executed to the highest standards. This research includes data management, programming, and statistical analysis of health claims, electronic medical records, and other observational data sources. The Director also keeps current with healthcare policies, RWE data trends Biopharmaceutical industry, and other developments with other....

- Greenville, SC

Reporting directly to the Quality Systems and Compliance manager, the Quality Auditor will have responsibility to audit scheduling, planning, execution and documentation of quality system audits of internal processes for the Greenville location. This position will also be responsible for maintaining a library of standards and for reviewing all applicable regulations, standards and communicating requirements to site leadership. This position will provide cGMP / GXP, technical and auditing....


We are looking for a Quality Assurance Document Control Associate to provide assistance with maintaining a GMP documentation system. Roles And ResponsibilitiesAssist in implementing information systems for managing document tracking, controlled document distribution (issuance) and records management.Oversee the issuance and maintenance of logbooks.Facilitate the final review of production batch records.Assist in administering the change control system (issuance, tracking, and....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Sales Representative for its industry leading analytical instrumentation used in R&D laboratories. This position will be responsible for direct sales of quality control laboratory instrumentation (density, concentration and viscosity instrumentation) and services to customers covering Delaware, Maryland, DC and the Northern Virginia area. Responsibilities:The Technical Sales Representative will....


Company is a not-for-profit healthcare organization with more than 19,500 employees working across ten hospital campuses, more than 40 physician practices and 50 outpatient and urgent care facilities throughout Monroe, Miami-Dade, Broward and Palm Beach counties. Everything we do, we do to the best of our ability. That includes supporting our team with extensive training programs, millions of dollars in tuition assistance, comprehensive benefits and more. Working within our award-winning....

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