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Director of Quality and Food Safety - Salem, OR QUALIFICATIONS:B.S. Degree in Microbiology, Food Science, or related discipline required; advanced degree (MS, PhD) preferred.Previous experience in Quality Assurance/Food Safety within a fresh food processing environment is preferred.Experience with audits at the plant and/or grower level.Must have experience in food safety, handling of fresh and frozen produce/perishables, BRC, HACCP, GMP, USDA, FDA and working with Federal and State....


Global Pharmaceutical company in Madison, New Jersey is looking for a Pharmacovigilance Agreements & Alliance Management Specialist We are looking for candidates with a PharmD or RN/NP with individual case safety report processing experience and knowledge of global drug safety/PV regulations, i.e., Drug Safety Associate/Sr. Associate/Manager. I. POSITION SUMMARY: The PV Agreements & Alliance Management (PAAM) Specialist guides and facilitates effective working relationships with....


New need for Growing Global Pharmaceutical Company in New Jersey Contract R&D Project Planner III This R&D Project Planner is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study timelines, providing evaluations of potential risks and conflicts, supporting the team on proactively resolving potential deviations, and presenting clear timeline reports. PP will work in a team orientated environment and is empowered to drive....


Global Pharmaceutical company is expanding in new offices in Madison, NJ This Clinical Trial Manager is an essential part of the Clinical Operations team. Looking for a strong Clinical Trials Professional with a operation experience for phase 2, 3 and 4 trials. Multiple therapeutic reas. -responsible for the delivery of studies , responsible for the execution and adherence of various aspects of the study operational plan (start up, conduct, close-out, and vendor oversight) with input from key....


Publicly Traded Top Tier Global Pharmaceutical Company is looking for a Clinical Study Manager or Senior level DOE to be located in their Cambridge, MA Headquarters competitive base salary and bonus, full relocation and stock and other long term incentives! This role requires a strong communicator: Duties and Responsibilities: 1.Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and Company SOPs, and supporting....


Large Global company is expanding their St. Louis team- They are in need of and Executive Director, Development In addition to a generous base salary: there is a bonus (30%) there is Equity Stock Grant Program and also Executives at this level have Stock purchase plan: (they can buy Stock options and company matches 75%) 3 weeks vacation PLUS – they ar eclosed during Christmas and New Years They will prvide FULL relocation This role reports into VP, Product Development Need Product Design....


New contract role (opportunity to convert to perm in future if desired) with Global Pharmaceutical company located in Cambridge, MA BACKGROUND: This Drug Product is an ALK Inhibitor for the treatment of patients with anaplastic lymphoma kinase-positive (ALK+) metastatic NSCLC. It was recently approved by the FDA under Accelerated Approval in April 2017, based on tumor response rate and duration of response, for previously treated anaplastic lymphoma kinase-positive (ALK+) metastatic....


Our mid-sized client is looking to add a Principal and Sr. Compliance Specialist to add to their growing team. The main responsibilities will be Field Corrective Action (FCA) and Recall Management for Medical Devices. Will be leading teams to develop field corrective action and recall plans. Oversee execution and reconciliation of field corrective actions and recalls. Working with cross-functional partners to determine root cause and population bounding as well as with Health Hazard....

- Bessemer, AL

Sr. Process Engineer - Full relocation benefits to near Northport/ Tuscaloosa/ Bessemer/ Birmingham AL The Sr Process Engineer reports directly to the VP of Manufacturing with plenty of autonomy and responsibility for a Chemical Engineer and “jack-of-all-trades in a chemical plant. Since this is a small plant, there will be duel technical and leadership responsibilities. Why might this be a good career move? Their future is bright: They make a very high demand product used in a large variety....

- Tampa, FL

Multinational Pharmaceutical and Device company with a focus on Neuro, Opthalmic, Dermatology, GI and branded products is expanding in their Tampa, Florida location This is a Packaging Engineer – reporting into a Manager Must have Pharmaceutical Packaging experience Solid communication and presentation skills preferred This is for a new line in the Opthalmic Division Will relocate to Tampa for this role Overview Provide packaging development and engineering support and expertise in the....


Medical director needed for Global Pharmaceutical company with US Headquarters in Massachusetts The role of the Medical Director, GPSI–US is to provide medical management and leadership for processing and analyzing safety reports for assigned compounds. The role is responsible for the overall safety assessment, pharmacovigilance activities, US label review, US periodic aggregate reports, and regulatory reporting activities for marketed/investigational products. The position also provides and....


Top Tier Global Pharmaceutical company in New Jersey is expanding: Looking for a strong Professional with Regulatory and Associate Director, Analytical Development bold, global pharmaceutical company and a leader in a new industry model – Growth Pharma. we are focused on developing, manufacturing and commercializing branded pharmaceuticals and biologic products for patients around the world. We market a portfolio of best-in-class products that provide novel treatments for the central nervous....


This position in the Clinical Programs department will be based in the Midwest, preferably in Minnesota, and is responsible for day-to-day field implementation of companies multi-center clinical investigations in accordance with corporate objectives, EU and FDA guidelines and protocols. The Field Clinical Engineer (FCE) is the primary site contact with respect to study recruitment, patient selection, and implant procedure support, requiring excellent clinical and technical skills. This....


Join a global leader as a Eco-Toxicologist responsible for conducting quantitative environmental risk assessments for agrichemical and fertilizer products and traits in North America. You will provide technical advice on study designs for regulatory and research oriented studies as well as advice to support new and existing registrations of client products and traits. --- Work closely with regional/global regulatory and product safety teams as well as other functional teams to produce risk....


Job Summary: Provides technical support for variety of activities related to new product development, product reformulations and other regulatory issues as they arise. Main focus of this position is to be the business partner between Regulatory Affairs and Product Development to address situations that arise on documentation for preliminary formulations, ingredient statements, nutrition and claims. Responsibilities:Serves as the point person for Regulatory Affairs and Research and Development....


Are you a BC MD or DO BC by an Approved ABMS Board certification by the American Board of Psychiatry and Neurology. Current state medical license without restrictions. This is and outstanding opportunity for someone who is interested in working a Utilization Review role in the Columbia, SC region. It is a plus if you have Medical Director experience or even experience working with a health plan company. This opportunity comes with a 20% (or higher) performance bonus structure and there is the....

- Elmsford, NY

Staff Biostatistician (Or Senior Staff - Depending on Level of Experience) East Coast (NY, NJ, or DE) Competitive Salary, Bonus, 6% 401K, 4 Weeks PTO, Excellent Benefits We have a newly created opening for an experienced Senior (Staff or Senior Staff Level) Biostatistician with a longstanding client; a multi-billion global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized,....


Reporting to the Director of Regulatory Affairs, this key role is to function as global lead on device teams. Ensure that submission content meets regulatory requirements. Strategize to identify risk areas and develop alternative courses of action. Manage scenario planning and development of regulators responses. Manage medical device Regulatory Affairs activities for developing global CMC medical device and IVD strategies across product life cycles & execution in North America. Support....


Are you a BC MD or DO BC by an Approved ABMS Board certification by the American Board of Psychiatry and Neurology. Current state medical license without restrictions. This is and outstanding opportunity for someone who is interested in working a Utilization Review role in the Columbus, OH region. It is a plus if you have Medical Director experience or even experience working with a health plan company. This opportunity comes with a 20% (or higher) performance bonus structure and there is the....

- Seattle or Tacoma, WA

Medical Director – Behavioral Health – Seattle Area New role in the organization will collaborate with the VP of Medical Affairs to direct and coordinate the physician component of the utilization management functions for the local health plan, with emphasis on the behavioral component of the integrated care programs. · Provides medical leadership for utilization management activities and medical review activities pertaining to utilization review, quality assurance, medical review of complex,....

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