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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....


Company is seeking a Principal Engineer to lead projects in the Biologics process development and clinical manufacturing projects. The individual will design, develop, scale-up and optimize drug substance and drug product unit operations for protein therapeutics. Experience managing projects from Discovery integration through GMP manufacturing, with both internal and external partners are required. The candidate should have strong technical, communication and interpersonal skills, be able to....

- Cambridge, MA

My client seeks an outstanding scientist to contribute to drug discovery and development projects. The ideal candidate will work closely with medicinal chemists and other scientists – and apply methods to improve drug properties and efficacy. In addition, this person will apply and develop cutting-edge techniques and interpret data using modeling and data mining. Finally, the ideal candidate will possess leadership qualities to direct projects and collaborations. The level of the position is....


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....


DEVOPS ENGINEER Enterprise Cloud Applications Location: Columbia MD REQUIREMENTS:Prior DevOps experienceExperience with SQL Strong working knowledge of Version Control (preferably with GIT)Ability to interpret and act on Java stacktrace errorsSolid communication skills (verbal & written) to communicate with business and technical customersMust be able to be on-call for infrequent high priority production server issuesMust be able to work flexible hours for occasional downtimes during off....


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.....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....


Our healthcare client is a leader in the field, and they seek to hire a Director of Product Marketing to manage a growing group and enhance their downstream marketing efforts. The ideal candidate will take on the following tasks: Actively support the worldwide selling efforts, including close collaboration with the field sales force.Provide product, competitive and clinical data analyses to global sales force.Create comprehensive marketing collateral based on clinical indication driven market....


Company BackgroundFor 30 years, this research laboratory has been manufacturing and distributing a variety of enzymes and cofactors used in coagulation research. Their sister diagnostics company provides general purpose and specialty assays to the clinical coagulation laboratory. This diagnostics division seeks an energetic Director of Research and Development with an entrepreneurial attitude and a desire to play an integral role in the growth of the company. Responsibilities: The Director of....


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....


Executive Director, Global Oncology Medical Affairs. Reporting the Chief Medical Officer, the Executive Medical Director will be accountable for the development and execution of the global medical affairs strategy. This physician will develop and lead the execution of global external engagement, communication and evidence generation strategies and will contribute to the overall global product strategy.This role is for a physician with at least ten plus years of oncology medical affairs....


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....


This position provides technical leadership and accountability for computer system validation and ensures compliance with internal and external computerized system policies and regulations. As the Subject Matter Expert, this individual will ensure sites are fundamentally aware of and proactively implement current computerized system validation practices with particular focus on impact to patient safety, product quality and record integrity. Position scope includes local and global site systems


Manufacturer of nutritional supplements, bars and protein powders. Responsibilities: Install, set up, configure, maintain and repair processing and packaging equipment in accordance with production requirements and scheduling with the ultimate goal of reducing equipment downtime. Receive daily work schedule from the Maintenance Supervisor, prioritize assigned duties and take required actions to ensure dependable and functional operation of machinery equipment. Fillers, hoppers, cappers,....


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....


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....


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....

- Any US State

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....

- 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....

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