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- Madison, NJ
new job!

Top Tier Pharmaceutical company (with focus in Cardio, respiratory, CNS, Psych and more) in Madison, NJ is looking for a new Director, Clinical Development for to add to this growing team!The Director Clinical Development will report directly to the Vice President and is responsible for the scientific, strategic, therapeutic, and operational management of programs to evaluate, register, and market pharmaceutical agents. Lead and direct study programs, activities, and teams for one or more....

- Jersey City, NJ
new job!

PHARMACEUTICAL COMPANY: focused on cns and GI and anti-infective The growth of this Corporation has created a unique opportunity for a variety of positions in Northern New Jersey, accommodating staff in Clinical Operations, Data Management, Biostatistics, Clinical SAS Programming and Regulatory. The Clinical Trials Manager will be able to organize and facilitate the overall planning, coordination and general performance of clinical trials that support the Clinical Development Plan for Clinical

- Wilmington, DE
new job!

Global Pharmaceutical company is hiring an Executive Director to head up their Renal Medical Affairs Division this Executive role will report into the Executive Vice President of Medical Affairs and spear head the high profil department must be Nephrologist with at least 3 years of medical affairs experience Renal Cardio Medical Head (Executive Director) The Renal Cardio Medical Head is a member of the Renal-Cardio Therapeutic Area (RCTA) leadership team and leads the Renal Cardio Core Medical


High Profile Pharmaceutical company with recent FDA one of a kind approval is hiring an Associate Director of Regulatory Affairs CMC The Associate Director, Regulatory Affairs CMC will lead development and implementation of global regulatory CMC strategy for Alnylam’s program(s) as a key member of multidisciplinary teams. This role will also lead the preparation of high quality regulatory submission content focusing on chemistry, manufacturing, and control (CMC) to support global clinical....

- Any US State
new job!

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,....

- Any US State
new job!

Pharmaceutical company hiring MSLs- GI and Pain and Addiction three pain/addiction roles to cover the whole United States in the: East, Central and West. There is one GI role for Texas region only please only apply if you have previous and recent Medical Science Liaison experience for the pharmaceutical or biotech or medical device industries looking for three or more years of experience as an MSL The Medical Science Liaison (MSL) plays a crucial role in Medical Affairs, being part of an....


Strategic opportunity as North American (NA) Team Leader supporting Analytical/ Synthesis (Methods Development); Product Metabolism, Product Safety (registration); 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 background in Scientific....

- New York, NY
new job!

Head of Gene Therapy CMC My client is expanding and looking to bring on a new person to lead CMC for Gene Therapy. The ideal candidate will take on the following tasks:Plan, lead and communicate the CMC related strategies for gene therapy products, including selecting CROs and CMOs.Actively manage CRO/CMOs for process optimization, scalable cGMP manufacture (both Drug Substance and Product) to supply a multi-product portfolio of pre-clinical and clinical gene therapy development....


We are in search of a FULL TIME Board certified or Board Eligible Family Medicine Physician to provide direct medical care to company employees and their dependents seeing ages 2 and up. The qualified candidate should have at least 2-3 years post residency experience, clinical leadership experience and working knowledge of Electronic Medical Records systems. THIS IS A BRAND NEW CLINIC/ NEWLY CREATED POSITION. We need a physician who will be able to start in November. It is a plus if you have....


We are in search of a FULL TIME Family Practice/ Primary Care, Internal Medicine or Family Medicine Physician to provide direct medical care to company employees and their family members.Unlike more traditional healthcare settings, our client's team members have the freedom to spend more time with their patients, while working alongside them every day. It’s a forward-thinking approach that allows them to provide best-in-class services, fostering stronger patient engagement and delivering....

- Edgewood, MD

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. General Responsibilities: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....

- 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. General Responsibilities: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....

- Chicago, IL

$25B Pharmaceutical Company—North Chicago—Salary Commensurate with Experience The SizzleCompany offers great work/life balance.Company offers competitive benefits and perks, including insurance, PTO and sick days, and work flexibility.Company prides itself on having a diverse and inclusive culture. Note from the Hiring ManagerWill provide relocation assistance for the right candidate.Will sponsor an existing H1B. Position Summary Seeking a Senior IT Auditor to be responsible for conducting....

- Orlando, FL

Position: Director of Nursing Location: Orlando FL SPECIFIC DUTIES & TASKS Active Treatment: · Oversees delivery of medical treatment to clients. · Oversees provision of dietary and dental services. · Complete clinical assessment to residents as needed. · Monitor weight charts, seizure records, lab reports, bowel habit records, fluid intake records, etc. to investigate and report significant changes to individual’s physician(s) and coordinate follow-up care as appropriate. · In partnership


We are looking for an experienced Environmental Water Quality Program Specialist (Project Manager / environmental lab / analytical). Duties and Responsibilities : Project set-up, Sample Receipt, Reporting, Account Maintenance- Provide courteous and efficient telephone and e-mail support to clients; Schedule/coordinate access and/or on-site escort for field staff; Interface/liaison between the lab and internal and external customers; Works with Lab Operations to ensure adequate capacity and....


Company is embarking on a $15M three year modernization of their facility and need to add several engineers to their staff. The modernization of the plant will include a new state of the art central process control room and modern office space, nutrition area, and open conference room. They are looking for: - Control Engineers, BSEE, PLC and SCADA systems, Siemens, WinCC PLC - Electrical Engineers, BSEE, project and maintenance - Mechanical Engineers, BSME, mostly maintenance and CapEx....

- Des Moines, IA

The Lead Controls Engineer will be responsible for virtually all of the technical work with respect to automation projects and services provided to a key customer. The role of Lead Controls Engineer comes with a variety of different responsibilities and options to pursue many career paths, including the potential for a role in opening an office in the Des Moines area. Responsibilities:Create, design and implement outstanding controls systems solutions for industryInterface with customers and....

- Rockville, MD

Leading Controls System Integrator specializing in Process Automation and Manufacturing Intelligence need to add a Sr. Project Engineer/ Sr. Controls Engineer to their team due to growth. Work from home in Washington DC area or Baltimore, MD. Why work here?:Stable company in business for over 30 yearsVariation of projects in many industries including Biotech, Pharmaceutical, Food Processing, Consumer Products, Water/Wastewater, Power, Oil & Gas, etc.Room for growthCompany known for....


A Business Development Manager with industrial process controls project experience is needed for a leading company in the Industrial Control Systems field that is one of the world's fastest growing Systems Integrators. They build and integrate world-class automation systems and solve unique and challenging manufacturing problems for customers in industries including Oil & Gas, Chemical, Petrochemical, Food, Pharmaceutical and Industrial Utilities. Why work here:Stable company in business....


Growing Industrial Automation Systems Integrator seeking Controls Project Engineers for their Indianapolis area office. Why work here?:20+ years in business with several offices in the Midwest85% repeat business with existing client baseVariety of projects in Pharmaceutical, Automotive, Food & Beverage, Consumer Goods, General ManufacturingAll engineers have cradle-to-grave involvement with their projectsAll Managers and Owners have worked as an Engineer in their careerKnown in the....

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