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We are looking for a Production Manager to be responsible for overall manufacturing and packaging. Major responsibilities include plant startup activities, such as building teams, qualification of equipment, setting up plant systems and processes, site transfer of manufacturing processes, media fills, maintaining aseptic manufacturing areas and manufacturing of exhibit and commercial batches. The Production Manager will ensure that manufacturing and packaging operations are carried out in....


Description:Position Title: Director of Business Development- Southern California Location: San Diego, Los Angeles (can commute to regional territory) Comp: OTE $225,000K Potential Year 1, Base $90,000-$140,000 for expertise with the Space. Base increase commensurate with CRO Services sales experience. Travel: Local Territory: Southern California with accounts in San Diego and Los Angeles Role: Business Development and Growth of Pre-Clinical Services Overview: Rapidly growing mid-size....


Description:Position Title: Director of Business Development- New England Location: Boston, Massachusetts Comp: OTE $225,000K Potential Year 1, Base $90,000-$140,000 for expertise with the Space. Base increase commensurate with CRO Services sales experience. Travel: Local Territory: Boston, MA with accounts in NH, CT Role: Business Development and Growth of Pre-Clinical Services Overview: Rapidly growing mid-size Pre-Clinical CRO is expanding into the Boston Market. Productive territory....


Technical Marketing Specialist Greater Philadelphia, PA (Bryn Mawr, PA) We have a new job opening for a Technical Marketing Specialist with a global market leader in the chemical/polymer industry. They are over 30+ years old, privately held, and are headquartered in the greater Philadelphia area. This organization has manufacturing facilities in the USA, China, Eastern Europe, and also operates in more than 40 countries. They have seen consistent steady growth over the years and offer an....

- Menlo Park, CA

Education and Qualifications - M.D. ; Specialization in Hematology/Blood Cancers. - Preferable five to seven years clinical or clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry. - Expertise in Phase I 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....


Our client is a fast-growing established world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative selling out client's line of microwave synthesis, extraction, and digestion instruments and will also include a line of Raman spectrometers. The territory includes Northern California, OR, WA, ID, MT, WY and northern Nevada. Candidates will ideally be located in the San Francisco bay area, but other major cities in the territory will be....

- Waltham, MA

TOP TIER PHARMACEUTICAL COMPANY in MASSACHUSETTSglobal biopharmaceutical company developing innovative medicines The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates Position SummaryWe have the need for a highly collaborative, experienced Manager of Medical Writing Operations to join our team based in MA. The position reports into our Director of Medical Writing and will lead writing responsibility of documents which ensure....


Leading Global Pharmaceutical company with office in Waltham Massachusetts Manager, Health Economics & Outcomes Research (HEOR) Position Summary: The Manager for Health Economics & Outcomes Research (HEOR), will be responsible for supporting HEOR activities for company's products. This individual will contribute to evidence generation, development of strategy, data analysis and dissemination and support the HEOR Senior team members (Directors, Senior Directors).....


Drug Product Process Engineer Small Molecule Continuous process Improvement for this leading pharmaceutical company in New England S Headquarters in Waltham, MA Looking for Senior Engineer for drug product unit operations- leadership scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Experience with continuous manufacturing, scale-up and PAT implementation is strongly desired. The individual is expected to integrate QbD principles, guide....


This full time, permanent Mechanical Project Engineering career opportunity is at a company that sets the industry quality standard. They design and build all their products in the United States. The engineers are known for being highly skilled and innovative. Projects are very diverse so the work here is interesting. Employees leave at 3:00 p.m. on Fridays. The successful candidate's duties and responsibilities will encompass:Analyzing and evaluating assigned projectsAssigning and giving....


This full time, permanent Mechanical Engineering Designer career opportunity is at a company that sets the industry quality standard. They design and build all their products in the United States. The engineers are known for being highly skilled and innovative. Projects are very diverse so the work here is interesting. Employees leave at 3:00 p.m. on Fridays. The successful candidate's duties and responsibilities will encompass:Designing detailed assembly and detailed fabrication drawings of....


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....


We are looking for a Quality Assurance Document Control Associate to provide assistance with maintaining a GMP documentation system. General Responsibilities:Assist 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....


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....


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....


We are looking for a Calibration / Instrument / Metrology Technician who will initiate, coordinate, and administer the calibration program for the facility. They will conduct/coordinate the inspection, calibration, and repair of all instruments, equipment and systems used for the manufacturing and measurement and determination of quality attributes of pharmaceutical products in accordance with current industry regulations and practices in the U.S.A. and the state of North Carolina.Under the....

- Lancaster, SC

We are looking for a qualified individual who has the understanding and knowledge of development of chromatographic, spectroscopic, titrimetric and wet chemistry methods. Implements strategies to ensure effective achievement of scientific objectives. Monitors and evaluates completion of tasks and projects.Roles and Responsibilities:Has hands on knowledge and can begin the development and validation of scientifically sound analytical methods for Product release and stability testing.Familiarity


We are looking for a Quality Control Analyst who will support the Quality Control group to maintain process optimization and manufacturing activities. This person will be reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in the QC lab with....


We are looking for Technical Document Reviewer with pharma experience. This position will be responsible for working within the Quality Systems organization supporting the review, development and implementation of harmonized documents, processes and systems. General Responsibilities:Review of documentation from various suppliers and other sites for use at site.Creation of site-specific specifications, standard test procedures, general test procedures, test data sheets and any other....

- Any US State

Position Summary: The Senior Director, CMC Regulatory Affairs will be responsible for providing CMC regulatory leadership and strategy across the organization and to our global partners. The Sr Director, CMC Regulatory Affairs will collaborate with the clinical development team, including the Chief Scientific Officer and drug substance and drug product manufacturers, and others for drug development and manufacturing in the pharmaceutical and biotech industry in accordance with the protocol,....

41-60 of 111 results