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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....


POSITION SUMMARY: Seeking an engineer to lead projects in support of small molecule clinical and commercial manufacturing processes. The individual will design, develop, scale-up and optimize robust drug product unit operations that provide high product quality at various scales ranging from R&D to cGMP manufacture. Strong collaboration is expected with internal early R&D groups, internal commercial partners, and external third party CMOs. The candidate should have strong communication

- Dallas, TX
new job!

Nationwide medical service company is expanding their imaging division. They are seeking someone with a strong hands-on multi-vendor CT and X-Ray service background. MRI service experience would be a plus but not required. The individual hired will be the imaging guru, responsible for the CT and X-Ray service, as well as the people who are servicing the CT and X-Ray equipment. Any manufacturer's training or RSTI training is a plus. Position is based in Dallas and will require some overnight....

- Dayton, OH
new job!

Growing healthcare network is in need of a CT/MRI service engineer, based in the Dayton Ohio area. MUST have mfg training and experience servicing multi-vendor CT & MRI instrumentation. Any experience with GE or Siemens CT/MRI is a definite plus. Become part of a team of imaging service professionals. Company will provide relocation assistance for a qualified service professional. Applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders....

- San Francisco, CA
new job!

My client seeks a Director of Business Development to provide exceptional service and care to their current and potential biotechnology and pharmaceutical clients. This person will meet with scientists, directors, VPs and CSOs of pharma and biotech firms, review their current R&D landscape, and offer solutions (both internal and external.) The focus of the position is to develop relationships with these potential clients, build rapport with their R&D groups, and grow into the role of....

- Almeda, TX
new job!

Senior Manufacturing Engineer Houston, TX (Southside / Local Candidates Preferred) Competitive Pay, Full Time Job, Benefits - Some Relocation Assistance Available Our client is a 30+ year old publically-traded global medical device manufacturer; with operations throughout North America, Europe, and Asia, as well as additional locations. They develop, manufacture, and distribute medical devices used in interventional and diagnostic procedures. We are looking for an experienced engineer with

- Neptune, NJ
new job!

Leading Controls System Integrator specializes in process automation and manufacturing intelligence need to add a Controls Engineer with some manufacturing IT experience to their team due to growth. If you are a Controls Engineer and have an interest in IIOT, Real-time production analytics, or Manufacturing Execution Systems (MES), then this could be ideal for your career. Why work here?:Stable company in business for over 30 yearsVariation of projects in many industries including Biotech,....

- Neptune, NJ
new job!

Leading Controls System Integrator specializes in process automation and manufacturing intelligence need to add a Sr. Controls Project Engineer to their team due to growth. 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 creating innovative products as well engineering projects3 weeks PTO per....

- Cranford, NJ
new job!

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....


Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....

- work from home, FL
new job!

Global Pharmaceutical company (headquarted in West Palm BEach, Florida) is growing and needs a Strong Clinical Lead (someone who mas managed the CRAs and the clinical study trials but can also monitor when needed as Snr CRA). Snr Clinical Research Associate for oncology trials. Must have five to eight years of experience with at least two years of oncology experience. Must come from a Sponsor company (Pharma or Biotech) and be bi-lingual (spanish speaking - many sites are in Latin America).....


The Manager Regulatory Affairs will be responsible for the following: Leading the preparation and filing of regulatory applications (IND, NDA, BLA).Coordinating/meeting with various functional areas in order to identify and obtain information required for regulatory submissions.Developing and/or reviewing regulatory documents (IND, NDA, BLA) in order to ensure that all submissions are of high quality.Leading the preparation of responses to questions from Regulatory Authorities.Developing and....


Our client cannot sponsor or transfer any work visa at this time You must currently live in the USA to apply RELOCATION PACKAGE High visibility role with a market leading medical device company. Work on next gen. product development. Hands-on role responsible for designing entire systems from user needs/requirements through design, verification/validation, transfer, and sustaining. REQUIEMENTS:MUST HAVE MEDICAL DEVICE EXPERIENCEBS Mech Eng, Elec Eng, or Biomedical Engineering, MS degree....


Our Client - a growing Pharmaceutical Company - is looking for a Quality Site Head - Pharmaceutical for their facility in NJ. The Quality Site Head - Pharmaceutical will be responsible for all QA activities supporting the manufacture of pharmaceutical products at the site. The Quality Site Head - Pharmaceutical will provide leadership for the Quality unit and as well as departmental personnel. The Quality Site Head - Pharmaceutical is responsible ensuring cGMP compliance by establishing and....


Top Tier Global Pharmaceutical company is expanding and looking for two Medical Director (for Clinical) must be Medical Doctor with MD degree Can have experience in oncology or even internal medicine and have experience with clinical development. Competitive salary and benefits and bonus, 401k, long term incentives and short term incentives and more Provide medical support for the study team:Global primary contact person during the course of the study for medical;Responsible for content of....


POSITION SUMMARY This position provides leadership to the Process Automation team in the IT Department engaged in the development and maintenance of the Automation Systems used in the production of drug products. The position collaborates with global business and IT colleagues to ensure long-term plans are established and implemented to ensure a robust and sustainable Process Automation program that is aligned with the strategic goals of the company. MAJOR RESPONSIBILITIESSet direction for the


Director Analytical Method Development & Validation (GMP BiopharmaceuticalPhD preferred or MS with LOTS (5+ mgt, 10+ GMP)Analytical Method Devt, qualification and validation experience requiredComplex and New Method workLarge Cell experience is a mustWould love to have protein Characterization and analyticsGMP and STRONG leadership (team up to 60-100), Financial Management


LOCAL CANDIDATES PREFERREDHands-on product development role for a market leading medical device company. Manage quick-turn projects from concept to production. Broad interactions internally and externally. REQUIREMENTS:BS degree in an Engineering discipline, MS preferredMedical device manufacturing experience; Extrusion experience highly preferredExperience bringing products from design through release to manufacturingCatheter/Balloon development experience


Specialty Pharmaceutical company is expanding the Somerset, NJ location- Looking for a Supervisor, QA Documentation This position serves as a dedicated resource for the administration of controlled documentation and documentation systems at the companys Somerset site. Associated documentation, systems and activities provide support for all facets of material, process and product development, validation, manufacture, testing, storage, service and distribution. It also applies to controlled....


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....

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