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- Elk Grove Village, IL
new job!

Our client is a well-established, growing company with a dynamic leadership team, offering an exciting opportunity for an experienced Manufacturing Engineer to join their organization. Our client is a low volume, high mix manufacturer of products for Medical Device, Aerospace and related industries. Highly competitive compensation packages are offered for high performing individuals! The Manufacturing Engineer develops and implements manufacturing processes to maintain proper functionality as....

- Myrtle Beach, SC
new job!

Our client is a dynamic medical device technology company, seeking a Senior Financial Analyst to join their growing team in Myrtle Beach. The Senior Financial Analyst will lead financial analysis, commercialization support, and financial modeling. This is a high visibility position working with senior management and is a core function with a direct link to the C-suite of a high growth company. Responsibilities of the Senior Financial Analyst:Support the finance and commercialization and....

- Southfield, MI
new job!

Embedded Software Engineer - ADAS Southeast MI Job Summary of the Embedded Software Engineer - ADAS: Embedded Software Engineer is required to play a key role in the design and development of the ECU software for Advanced Driver Assistance System for our client in Michigan area. This is a stable, growing company offering significant future opportunities to break into new technologies. If you have Embedded or real-time software and device driver development experience, then this position is....

- Irvine, CA
new job!

WPIJP00008461 - Clinical Trial Manager 09-24-2018 to 09-23-2019 WPIJP00008485 - Clinical Trial Manager 10-01-2018 to 03-15-2019 These are contingent worker situations expected to last 1 year. Qualifications - B.S. degree. - Minimum of 3 to 5 years of pharmaceuticals/biotech experience. - Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. - Process and system....

- Menlo Park, CA
new job!

Qualifications - 12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff. - Industry experience within pharmaceutical and/or biologics and prior experience in FDA negotiations relating to the conduct of regulated clinical trials. - Comprehensive understanding of applicable clinical research regulations. Thorough knowledge of GCP, ICH guidelines and other

- New Jersey, NJ
new job!

Plan and prepare complex medical device regulatory submission documents for US, Canada, and EU regulatory filings. Provide support for other global regulatory filings. Utilizing detailed, in-depth understanding of medical device regulations, leads and participates in global regulatory teams, interprets regulations, and provides regulatory guidance. Supports management with regulatory programs planning and implementation of departmental strategies and policies.

- Menlo Park, CA
new job!

Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical Trials Requirements Bachelor’s Degree in life sciences or healthcare field. Additional coursework in clinical trial design.Ability to travel as required (up to 25%).12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff.Industry experience within pharmaceutical....

- Northern, CA
new job!

Responsibilities Manage, develop, and train the GCP Compliance personnel. Ensure the integrity and quality of clinical data by overseeing all routine and directed; internal and external; domestic and international GCP audits and quality reviews. Promote continuous improvements in quality systems and department infrastructure. Act as a subject matter expert and provide GCP guidance to internal departments for all phases of clinical development. Report significant and/or serious ongoing quality....

- Brea, CA
new job!

Local 30-year old manufacturing company is searching for a Materials Sourcing/Logistics Manager for their facility in Brea, CA. The company is a Medical Device Manufacturer and services a variety of hospitals and clinics in both domestic and International markets. You must have Domestic & International sourcing and/or supply chain experience in the Medical Device industry in order to be considered. RESPONSIBILITIES:Source the best resources at the best pricesKeep the manufacturing process....


Process Controls Engineers with DeltaV experience needed for reputable award-winning Automation and Control Systems Integration company. Great chance to use your industrial automation experience within the Biotech, Pharmaceutical, and Food and Beverage industries. Why work here?:Stable business for 25 years and growing!Fun and professional environment with over 120 employees!Variety of projects in several industries, many pharmaceutical and biotech projects!Training provided on new technology....

- Kalamazoo, MI
new job!

Automation Engineers needed for a growing and successful systems integrator in the pharmaceutical, chemical, food/beverage, medical device, and general manufacturing industries. Travel is low, typically 10% but will fluctuate from time to time with projects. The Automaton Engineer in this position will be responsible for the automation, start-up, troubleshooting, and commissioning of various manufacturing equipment and related systems. Looking for a team player who will enjoy working with....


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 Neptune, NJ office or from home in 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....

- Stevensville, MI, MI

Embedded Applications Engineer Stevensville, MI Summary of the Embedded Applications Engineer Job: For the last 27 years we have specialized in the electronic/software/hardware side of devices, and we have never seen anything quite like this opportunity for career changing growth. A long term Fortune 500 client of ours has engaged us to locate team members to be part of their advanced development projects. They develop cutting-edge applications that will change their industry. This is both a....


Power Electronic Systems Engineer Stevensville, MI Job Summary of the Power Electronic Systems Engineer: We need a top preforming Power Electronics Engineer to play a key role in our Client’s software driven electro-mechanical systems comprised of: motors, power components, battery charging and manangement systems (BMS), wireless networking and mechanical interfaces. You will play a vital role in the total system design as part of an advanced New Product Development Team (NPD). This is a....


Great opportunity to join a global industry leader, as the champion for strategic development and management of the Global Bioinformatics Group. As the Group Leader, you will drive the innovation of bioinformatics and genomics capabilities for research, development and delivery of products for multiple sites. The successful Leader will have a Ph.D in bioinformatics, genomics, or computational biology, and 10+ years experience in industrial biotechnology or related Industrial R&D life....


Our client is a growing global, research-based biopharmaceutical company that combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long-established pharmaceutical leader to develop and market advanced therapies that address some of the world’s most complex and serious diseases. with approximately 21,000 people worldwide and markets medicines in more than 170 countries Due to expanding product lines and a new standards lab located at Corp....


Software Project Manager West Chester, NY - Relocation provided Competitive Salary + 10% target bonus, 6% 401K Match, 4 Weeks PTO, Great Benefits We have an immediate opening for an experienced Project Manager with a longstanding client; a multi-billion dollar global medical instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that impact people's lives. A lot of the work


Represents Regulatory Affairs for pharmaceutical development projects and marketed products. Responsible for development and communication of all aspects of global regulatory strategy on R&D project teams. Leads team of regulatory professionals to assure successful planning and completion of regulatory activities on a worldwide basis. Responsible for knowledge of regulatory requirements of major regions (e.g. US, EU JP) with responsibility for working with colleagues on a worldwide basis....

- Any US State

The role of the Principal Writer, Medical Writing, is to prepare high quality clinical documents and to oversee medical writing responsibilities for multiple programs within an assigned therapeutic area (TA) of Global Branded R&D (including, as appropriate, drugs, biologics, and devices). In this position, the incumbent manages the planning and preparation of high-quality clinical documents (eg, clinical study reports, briefing books, clinical protocols, integrated summaries) and ensures....


* Background with CNC / Swiss CNC machining within a precision environment needed. * Ability to program, setup and troubleshoot CNC lathes and mills. * Ensure that all employees are working in a safe manner and that all safety related policies and procedures are being adhered to at all time. * Conducting daily safety walks within the department to identify any unsafe condition and taking corrective action. * Ensure that all quality related policies are being adhered to and that all processes....

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