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- Grand Rapids, MI
new job!

Logistics Director *** Please use our project code 0614-B when submitting credentials ****** My client located in a town about 30 Miles from Grand Rapids, Michigan is looking for a Logistics Director. They are one of the most technologically advanced manufacturers of heating related products in the world. They have roughly 1000 employees. They ship Worldwide. Responsibilities of position: The Ideal candidate will be responsible for oversight of all logistics management functions including....

- Seattle OR San Fran, Cali, WA
new job!

Top tier Pharmaceutical company in Seattle, WA is expanding They are opening new office as well i nthe San Francisco Bay area of Califronia- this role can be located in either location Full benefits-medical/health, 401k and match, stock, LTis and STis...many progressive benefits...competitive compensation and bonus and more... Full relocation to either area The Sr. Director, Clinical Operations Program Management will be responsible for leading all aspects of clinical operations within the....

- Jersey City, NJ
new job!

Top Tier Global Pharmaceutical Company is looking for a Supervisor for Print PRoduction= this is a w-2 contract (for one year and then up for renewal)- includes health, Medical benefits, vacation and more Company is in Jersey City and is moving to Madison, NJ in October (position sits in JC for now and then Madison) Oversees print production of promotional collateral from development to final distribution. Collaborates with creative agencies, marketing teams, and vendors to develop....


Top tier Pharmaceutical company (one n Boston and one in NJ nd one in Seattle)Required:Has completed management of a study or group of studies from planning through close out (Phase 3)Experience with managing VendorsExperience working on global studies with CROs Nice to Have:Experience supporting writing clinical study reports,Supporting sNDA or NDA submissions, Supporting pre-Inspection preparation,Participating in Sponsor Inspections by Regulatory BodiesExperience managing or leading teams....

- Jacksonville, NC
new job!

Nationwide service organization specializing in servicing biomedical & medical imaging equipment is in need of a BMET II in the Jacksonville NC area.Will be part of a multi-person biomed shop. Need to have formal training/education to service biomed instrumentation. People who have completed the military biomed training school are highly desired. Any manufacturers training is a plus. Applicants have to be authorized to work in the US without Visa Sponsorship. US citizens and Green Card....

- Charlotte, NC
new job!

Join this growing international company's dental division. You will be servicing, installing, testing and refurbishing dental x-ray systems and sub-systems. The company is looking for the following requirements:Minimum 2 years experience servicing biomedical instrumentation.Experience working with x-ray emitting devices (medical or industrial)Open to travel, with some overnight travel required.Networking & DICOM experience (this is a must).Ability to work well with minimum....

- Wyckoff, NJ
new job!

My client offers an outstanding culture and exceptional benefits, and they seek a Manager of Technical Writing to oversee a small group and take on the following tasks:Direct the overall process for creating, editing and publishing client reportsOversee variable workload by assigning and coordinating the work of othersEnsure the timely preparation of all manuscripts and responses to reviewer commentsServe as the internal editor-in-chief to establish and maintain a high-quality written....

- Providence, RI
new job!

This position is for a thin films sustaining process engineer specifically focused on Cathodic Arc and DC Magnetron Sputtered films applied in a fast paced job shop' environment. Expected to quickly become the technical expert on the process and equipment in the plant. Routine monitoring of equipment and process performance, defect analysis and defect reduction. Identify, respond to, and characterize equipment/process and quality/defect issues. Implement root cause solutions to those issues,....

- San Diego, CA
new job!

Op Ex Manager Looking for an OP EX Manager for a medical diagnostics company in San Diego. You must have managed a continuous improvement program. Will lead process improvement projects across a wide spectrum at the company's flagship site in San Diego, CA. The Continuous Improvement Specialist will develop, lead and manage Lean Six Sigma - LSS - initiatives, driving operational excellence and a continuous improvement culture. The Continuous Improvement Specialist will have the opportunity to....

- Petaluma, CA
new job!

Business Process Manager-Petaluma CA Dedicated to business process re engineering (analysis, mapping and optimization) to enable the routine delivery of exceptional business process performance. This position is within the Global Engineering and Facilities Services function of Supply Chain and supports operational improvement initiatives.). You will collaborate with Business Process Owners (BPO) to prioritize and drive business process improvements. The role reports into the Executive....

- San Francisco, CA
new job!

Vice President, Regulatory Affairs San Francisco Bay Area Our client is seeking a Vice President, Regulatory Affairs who will be responsible for regulatory strategy, oversight, and guidance drug development program. The successful candidate will bring strong leadership abilities to oversee the Regulatory Affairs team, a successful history of effectively leading IND and NDA filings through approval, and interacting effectively with the FDA and other foreign regulatory bodies. This position....

- Columbus, OH
new job!

My client seeks a manager to assist with educating physicians in academia and teaching hospitals. The ideal candidate will take on the following tasks:Create and deliver training programs for new physicians in electrophysiology, interventional cardiology, heart failure, general cardiology and surgeryEducate clients on the clinical evidence demonstrating efficacy of the productPartner with internal leadership to help create road map to expand utilizationDrive adoption by developing consultative

- Charlotte, NC
new job!

My client seeks a manager to assist with educating physicians in academia and teaching hospitals. The ideal candidate will take on the following tasks:Create and deliver training programs for new physicians in electrophysiology, interventional cardiology, heart failure, general cardiology and surgeryEducate clients on the clinical evidence demonstrating efficacy of the productPartner with internal leadership to help create road map to expand utilizationDrive adoption by developing consultative

- Cincinnati, OH

The holder of this position is charged with leading effort to prove control of the critical aspects of company operations, whether these relate to process, cleaning, equipment, utilities, computers or other elements. Subject matter expert in at least two main area of validation ( Process/Cleaning/Equipment /Utilities /Facilities/Computer Systems)Lead and structure scientific debate and assessment with peers from other technical areas to develop scientific understandingDetermine levels of....


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

- Cincinnati, OH

Job Description: Responsibilities include supporting daily compliance and systems activities. Performs audits (internal and vendor audits), supports change control program, complaints and any customer services related to Documentation Center. Also works with manufacturing to identify resolution to events while working with Quality Management. The candidate will perform general QA work, using their ability as a skilled contributor in completing tasks where judgment is required in resolving....


The positions serves as the site’s Oral Solid Dosage (OSD) platform leader and reports directly to the Sr. Director of Process Development. Responsibilities include management and oversight of multiple early and late stage development projects and support personnel. Job Functions: Demonstrates technical expertise in OSD technology and methodologies. Lead site related process development, scale-up, commercialization and tech transfer responsibilities Collaboratively develop project strategies....


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....

- Buffalo, NY

Provides quality oversight to the Chemistry & microbiology laboratories and product transfer by supporting all work. Work in partnership with the aforementioned groups to produce quality work in compliance with all applicable regulations. - Review/approve deviations, OOS's, OOT's, EE's, and change controls. - Perform audits of the chem & micro labs. - Review/approve protocols, investigative studies, raw data and reports. - Establish and control quality programs to ensure conformance....


POSITION SUMMARY: Working with minimal supervision, manage complex projects/products, including responsibility for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies. Applies regulatory expertise to the evaluation and solution of product development issues. SPECIFIC DUTIES AND RESPONSIBILITIES: - Draft, assemble, and file original documentation and submission materials for new

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