Biotech, R&D, Science category and Medical Devices and Supplies industry jobs

We are looking for an Analytical Chemist for a growing medical device company in Atlanta. He/she will develop specific work plans to include primarily writing, organizing and executing analytical method validation, development, and transfer. Will also provide support to quality control laboratories to include routine use of HPLC, GC, UV/Vis, Wet Chemistry or some combination. May assist team on Qu...
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Our client has an exciting career opportunity for a Global Regulatory Manager to join a pioneer in developing therapeutic products for the tissue protection healing and repair. Reporting to the VP of Regulatory & Clinical Affairs you will help to implement the regulatory strategy to move products to approval while remaining in compliance with applicable regulations and guidelines in this collabora...
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1812PMW Senior Director, Clinical Development Operations Location: Philadelphia Area Salary: Up to $200K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking a Senior Director, Clinical Development Operations that will provide effective leadership, oversight and mentoring of the global clinical operations department thereby maximizing...
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Title: Mechanical Engineer (Exempt) (Professional) Description: Position is to support Sustaining Engineering in the R&D group. Product redesign, end of life component replacement and other projects as assigned. primarily looking for someone with a Mechanical or Biomedical Engineering background. . Develop prototypes, verification/validation units and product specifications, including material spe...
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1813PMW Assistant Director of Regulatory Affairs, CMC Location: Philadelphia Area Salary: Up to $130K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking an Assistant Director, Global Regulatory CMC that will be responsible for managing and maintaining multiple US and international (including emerging market) registration dossiers wh...
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1814PMW Assistant Director, Clinical Development Operations, Emerging Markets Location: Philadelphia Area Salary: Up to $130K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking an Assistant Director, Clinical Development Operations, Emerging Markets to oversee the management of Phase I through IV clinical research studies conducted ...
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1811PMW Director of Regulatory Affairs Location: Philadelphia Area Salary: Up to $160K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking a Director, Regulatory Affairs to provide oversight, direction and leadership for all regulaotry activities related to assigned therapeutic areas. WHAT WILL YOU DO HERE? - Develop regulatory strat...
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We’ve been engaged by our client to recruit their Principal Regulatory Affairs Specialist. This medical device company is looking for a candidate with at least 10 years of regulatory affairs experience and at least 6 years of experience within the medical device industry. Ideal candidates will have international regulatory experience, particularly in Latin American countries and Japan. Responsibil...
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We have been engaged by our client to recruit their Clinical Program Manager. Our client is a Fortune 500 worldwide medical device manufacturer with a deep portfolio of products. The Clinical Program Manager is responsible for developing clinical investigation strategy congruent with the Cardiovascular Division business objectives. Manage clinical study design and implementation with respect to pr...
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Job Summary: Position is responsible for ensuring that clinical research compliance is maintained for clinical trials in domestic and international countries. Essential Duties: Thorough knowledge of Good Clinical Practices. Monitor assigned clinical investigational sites which includes source document verification, device inventory records review and physical count, case report form review, verifi...
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We are looking for experienced Quality Control Analysts for a growing medical device company in the Fort Worth, Texas area for one year contract positions – all shifts available. Will provide support to quality and production laboratories to include routine use of HPLC, GC, UV/Vis, Wet Chemistry or some combination. May assist team on Quality Control sample checks and revise documents under the di...
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Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: MA - Walpole Req ID: 119470 Position Title: Biostatistician, Sr Experience Level: Senior Level Education Required: Bachelors Degree Travel Required: Yes Company Description: Siemens’ Healthcare Sector is one of the world's largest suppliers to the healthcare industry and a leader in medical imaging, laboratory diag...
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Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: CA - West Sacramento Req ID: 122682 Position Title: Test Manager - Systems Integration Group Experience Level: Senior Level Education Required: Bachelors Degree or equivalent experience Travel Required: No Company Description: Siemens Healthcare Diagnostics Inc. offers a broad portfolio of performance-driven diagno...
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Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: CA - Berkeley Req ID: 120710 Position Title: Sr. Requirements Engineer - Healthcare Diagnostics/Medical Device Experience Level: Senior Level Education Required: Bachelors Degree Travel Required: Yes Company Description: Siemens Healthcare Diagnostics Inc. offers a broad portfolio of performance-driven diagnostic s...
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Our client has an exciting opportunity for the experienced Manager Aseptic Manufacturing with strong leadership and strategic planning experience to join this pioneer in their field. In this challenging position you will be responsible for commercial manufacturing operations for pharmaceutical products. The key components are to provide leadership and direction for all Manufacturing personnel in p...
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Job Description Cincinnati OH R&D Manager General Summary This individual has full responsibility for the planning, organization, technical interpretation, and cross-functional execution of assigned projects. This includes supervisory responsibilities for a multidiscipline staff of engineers and technicians as well as coordination of the activities of a cross-functional team. Principal Duties and ...
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TITLE: Reagent Formulation Associate REPORTS TO: Larry Rea- VP Operations SALARY RANGE: Commensurate with experience Company Overview: Great Basin Corporation (GBC),a startup focused on rapid molecular diagnostics is seeking lab technicians for its research lab in Salt Lake City, UT. We are a young company with exciting patent-pending technology for the fast growing point-of-care diagnostics marke...
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The unblinded CRA will need to have worked in an unblinded role for at least 3 years min. understand drug accounts and needs to be a real go getter. Therapeutic area of CNS and MS experience. Requirements: · BS Life Sciences or RN · 5+ years of experience in a clinical operations role · 3+ years of experience working as an un-blinded CRA on clinical trials · Experience working with biologics in th...
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Description of Work: St. Jude Medical develops innovative products that reduce health care costs and improve outcomes for cardiac, neurological and chronic pain patients who suffer from epidemic diseases. Headquartered in St. Paul, Minnesota, St. Jude Medical employs approximately 16,000 people worldwide. Technology drives St. Jude Medical's marketplace success, but it is the people of St. Jude Me...
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The Senior Design Assurance Engineer (DAE) provides technical leadership and support to new product development and post commercialization. The Senior. DAE focuses on design related projects and deliverables required by the Product Development Process (PDP) as well as activities related to monitoring health of the product post commercialization. The Senior DAE may also provide project management, ...
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Quality Specialist needed for 1st shift to perform a variety of assignments within the QC laboratory in support of assigned plant operations to ensure the highest standards are met according to cGMP/GLP, USP and EPA regulations for products. Develop and validate methods such as Bacteriostasis and Fungistasis, test, inhibition and enhancement testing. Collect environmental samples and perform analy...
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We’ve been engaged by our client to recruit their Sr. Clinical Research Associate. This position is responsible for assisting with the design and execution of high quality clinical trials to ensure the safety and performance of the company’s products. Coordinate the overall administration of clinical trials including study design, project tracking, CRO oversight, monitoring plans, review of monito...
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Mechanical Engineer – North Carolina Resumes to: nancyc@directhr.com My client is an international leading in vitro diagnostics corporation. They design, develop, produce, and market diagnosis systems for the medical and industrial application in the labs. They are a world leader in microbiology, to respond to major public health issues, and affirm its position as a key player in clinical diagnost...
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LipoScience is a diagnostic company, working with practicing clinicians and the world's leading researchers to help identify patients with an increased risk of cardiovascular disease, using advanced computer analysis in combination with nuclear magnetic resonance technology. LipoScience provides equal employment opportunities to all employees and applicants for employment without regard to race, c...
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5+ years experience Experience overseeing vendors SDTM knowledge/experience EDC database setup experience Overseeing vendor Data Management activities for outsourced clinical trials, supervising database builds, all data cleaning activities leading up to database lock, and the development of submission-ready datasets. SDTM experience preferred. 3 month contract About Joulé Clinical Staffing At Jou...
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