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Global Pharmaceutical company with high profile trials is expanding and looking for a Director, Regulatory Affairs for their Global Management Team Competitive base salary and bonus, full relocation and benefits, Long Term Incentives and more Position IDEALLY is located in the Cambridge, MA office (there is small possibility the role can be based in their NJ office) The Rare Disease Global Regulatory Team Lead (GRTL) is part of the Global Regulatory Affairs (GRA) team based in the US. He/she....


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....

- Clearwater/St. Louis, MO, FL

Global Leader in Pharmaceuticals and Medical Devices is expanding in their Regulatory Affairs High Profile Division- Medical Device/CMC Position can be located in either the St. Louis, Missouri office or their Clearwater, Florida office relocation is provided Candidate MUST have Medical Device experience and must have written CMC submissions in the past (recent past is preferred) Individual Contributor role competitive base salary, plus bonus, full benefits and other Long Term Incentives.......


Top Tier Pharmaceutical company is growing and needs a Strong Clinical Research Associate for the East Coast (must be located in the Danbury, CT area to be in house, Headquarters when needed) leading developer, manufacturer and supplier of premium molecular diagnostic products and services that are used to diagnose human diseases, screen donated human blood and to aid in biomedical research. Our business is dedicated to impacting the lives of people across the globe through the early detection


Great opportunity to join a Global Company as the strategic North American (NA) Team Leader supporting Analytical/ Synthesis (Methods Development); Product Metabolism, Product Safety Standards; and Regulatory Compliance (EPA). Participate on the Global Leadership Team while developing a challenged, problem-solving analytical team responsible for performing/ delivering scientific studies to ensure a sustainable product safety and registration success. The successful candidate will have a strong

- Palo Alto, CA

The Senior Director is primarily accountable for nonclinical toxicology, working in collaboration with nonclinical pharmacology and pharmacokinetic scientists to drive the overall global nonclinical regulatory submission strategy and coordination for multiple portfolio products, from research to registration and beyond. The individual has experience in evaluating and responding to inquiries from regulatory authorities addressing global nonclinical development issues in support of IND and....


Our client is a major worldwide consumer products company, ranked in the Fortune 200. Indeed.com identified them as one of 25 of the biggest and brightest corporations that are going the extra mile to help employees achieve the elusive “work-life balance.” Fortune Magazine identifies them as one of the top 50 World's Most Admired Companies. Position Summary: This key corporate food safety position plays a critical part by participating in strategic planning & addressing major Company....

- 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....


Global Pharmaceutical Company out of Madison, NJ and Irvine, CA Position Summary: (Irvine, CA or Madison, NJ) Responsible for leading internal and outsourced Clinical Programming activities in support of Clinical Research studies and managing the design, development, validation, implementation, and oversees ongoing support to electronic case report form (eCRF) systems (e.g. InForm, etc.), external data acquisitions, reporting/business intelligence tools (e.g. SpotFire, J-Review), and other....


Are you a BC MD or DO BC by an Approved ABMS Board in Psychiatry (and familiar with Medicare patients) who is ready for a change? This is and outstanding opportunity for someone who is interested in working a Utilization Review role in the Las Vegas region. It is required you have a Nevada license that is in good standing. It is a plus if you have Medical Director experience or even experience working with a health plan company. REQUIREMENTS:5+ years experience working in a behavioral....


High Profile Drug Development Pharmaceutical Company is expanding: Global Category Director- Drug Development Services Are you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future Join us as a Global Category Director – Outsourced Drug Development in our Cambridge, MA office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Global Category Director

- Lancaster, SC

Summary of the Position:. Develops and deploys the quality system for entire manufacturing facilities to assure systems and procedures are compliant pursuant to government regulations, industry standards and Company specifications and policies. Periodically reviews the suitability and effectiveness of the quality systems with Executive Management. He/She has ultimate responsibility for making the quality decisions on the identity, purity, strength or composition of nutritional products in the....


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....


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....


Our client is a producer of Bio-pharmaceuticals. They have developed core competencies in the development of processes and products derived from natural sources both animal-based and plant-based. They have an immediate opening for a Regulatory Affairs Specialist. RESPONSIBILITIES:This position will provide regulatory support for development and commercial programs.In this role, you will plan, coordinate and oversee regulatory activities.These activities include the preparation of document....


Global Pharmaceutical company in Northern NJ is expanding and is looking for Packaging Mechanic Serialization Our company is a niche pharmaceutical company that develops, manufactures and markets generic and branded prescription pharmaceuticals as well as animal and consumer health products. We specialize in difficult-to-manufacture sterile and non-sterile dosage forms including: ophthalmic, injectables, oral liquids, OTCs, topicals, inhalants, and nasal sprays. We market our products to....


Global Pharmaceutical company is expanding: OBJECTIVES: - The Project Manager is required to identify and resolve project risks with proposed resolution plan (ad hoc and planned), with escalation to senior stakeholders where appropriate. - They will execute their day-to-day activities in line with company Category Management Framework, with a strong focus on strategic sourcing initiatives which aim to qualify and select suppliers that meet the needs of the business at maximum financial....


DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....


This is a key position that will have product development oversight responsibility for Design Control as the product moves through the development stages to commercialization. Key liaison between Product Development, Quality Engineering, and Regulatory Affairs. Maintain focus on VOC requirements as defined by Marketing. Required Background & Experience:MEDICAL DEVICE PRODUCT DEVELOPMENT EXPERIENCEBS degree in a technical discipline, preferably engineering. Advanced degree is a plus.Strong....


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....

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