(US-Michigan-Ann Arbor) We have a client in Ann Arbor that has asks us to assist them in finding the candidates for an opening that they have. This is a contract to direct hire position and below are all of the details. If this looks like something that you or someone that you may know of would be interested in looking into please dont hesitate to contact me. Thank you for your time and I hope that we will be able to do something for you. JOB SUMMARY: Work within a cross-functional team comprised of Design, Marketing, Regulatory, Manufacturing and Service to design, develop, test, market release, and scale-up new electromechanical, embedded systems medical devices. Responsible for insuring Quality and Reliability methods and processes are effectively incorporated and utilized throughout the development process. This includes use of tools such as Hazard Analysis, FMEA, requirements traceability, HALT, MTBF and reliability test methods. Responsible for product validation test plans and implementation. Work with the team to establish successful transfer to Manufacturing including assisting in establishment of inspection and test methods. Assist team with compliance to applicable standards and successful completion of regulatory submissions. KNOWLEDGE/SKILLS/EXPERIENCE REQUIRED: Minimum Bachelor’s degree in electrical, mechanical or biomedical engineering. Preferred electrical. Demonstrated experience with design and test of electromechanical embedded systems. Experience with a structured new product development system and demonstrated knowledge of product validation test methods. Demonstrated knowledge of risk management methods and tools including FMEA and Hazard Analysis. Knowledge of reliability tools and methods, including HALT and MTBF. Demonstrated interpersonal and cross-functional teamwork skills. Demonstrated effective verbal and written communication skills. Knowledge of relevant standards for electromechanical devices such as UL, IEC, IEEE, CSA, TUV. Working knowledge of FDA GMP/QSR. Work Experience 3-5 Years experience with electromechanical embedded systems Quality/Product Assurance and Product Development. At least 3 years experience leading and planning Quality activities and methods in a development project, including Hazard Analysis and FMEA. Previous experience leading a validation testing effort that resulted in the release of a successful new product. Medical device experience a big plus.
(US-Connecticut) Our client, a major pharmaceutical company in New London, CT is looking for a SAFE Sr. Business Analyst with the following qualifications: Senior Business Analyst with 15+ years experience with Physical Security (Badging/Security-controlled Access), Logical Security (NT User ID/PKI/Digital Certificates) and Remote Access (SecureID/Token Access) in a multi-site multi national commercial environment. B/A will be engaged to produce a financial assessment of the Total Cost of Ownership (TCO) of various aspects of a security proof of concept effort now under way. Need is immediate. Engagement will run through the end of 2003, with a possible 3 month extension to follow. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-Connecticut) Several outstanding opportunities are available in Fairfield County for pharmaceutical professionals. Seeking Triage Associate, Clinical Application Support Specialist, Med/DRA SOP Manager, several positions for Scientists, Research Associates, Toxicology or Pathology professionals and Animal Health Technologist. Excellent compensation packages and relocation available.
(Finland) Applications are invited for a biotechnologist/biochemist/molecular biologist position (M.Sc. or Ph.D.) in the Carbonic Anhydrase research group. The work relates to knockout technology, and therefore, strong experience in techniques of molecular biology is expected from candidates.
