The Quality Engineer will play a critical role within the manufacturing plant and will function as the subject matter expert on matters related to quality and regulatory affairs.
You will prepare, update, maintain and approve all PPAP documentation both for customer and supplier submissions.
You will design simple check fixtures for single features such as length, diameter, height, etc.
You will resolve all quality related issues with customers and vendors by analyzing ...
THIS IS A PERMANENT, ON-SITE JOB IN EITHER PEARL RIVER, NY OR MERIDEN, CT
The Senior Cluster Statistician assumes the role of an independent Statistician and is responsible for all statistical aspects of individual clinical trials within a vaccine cluster.
* Provides expert consultation and advice in quantitative/statistical, experimental design, and data management issues. Works with the clinical monitor and team to develop clinical protocols, analysis plans and final study ...
The Contract Manufacturing Associate is responsible for maintaining stability data in the regulated systems, organizing records and creating databases to track manufacturing parameters. This individual is responsible for assisting with vendor relationship management, new vendor evaluation, and resolution of any technical and quality issues that may occur during manufacturing campaigns. The Contract Manufacturing Associate interacts with the Research and Development, Regulatory Affairs, Technical ...
:: If you meet the qualifications listed below and would like more information contact Kristine at 815-756-1221. Attach resume when responding to this posting ::
The Manager will be responsible for providing lead scientific and regulatory partnership and support for global innovation and growth R&D projects. 25% travel
-BS-PhD in food science; advanced degree preferred
-5+ years of applicable experience
-Excellent communication skills
-US CITIZEN/PERM RESIDENT
We are looking to fill these positions related to Agricultural Chemicals and Ag Biotech
Regulatory Affairs Managers 3 to 20+ years depending on which role.
Regulatory/Registrations Managers 5 to 15 years Ag Chemicals or Ag Biotech.
Regulatory Affairs / Government Affairs 10 +years in similar role.
Regulatory Scientists with Eco Tox, EFate or Mammalian Tox studies , we have needs for Sr, Mid and Jr level positions.
Positions are ranging from 90K to 200k+ total comp, full corporate benefits ...
Opportunities located in: NY, NJ, PA, MA, NC
Responsible for the overall planning and direction of clinical regulatory activities. Develops and implements strategies with the goal of approval of regulatory submission.
Direct and oversee short-term and long-term planning of regulatory submission initiatives.
Interpret corporate policy.
Develop and implement strategies for the earliest possible approval of regulatory submission.
Manage regulatory teams and ...
Our client is a division of a global Medical Device manufacturer, seeking a Project Manager who will be responsible for delivery and launch of Medical Devices to the market. Projects will include enhancements to existing products as well as new product launches. The Project Manager will lead these efforts by leading cross-functional teams and ensuring that each team member is completing their assigned tasks in a timely manner to achieve project goals.
Works with cross-functional ...
NW Recruiters is seeking a Vice President of Global Regulatory Affairs. This role will be responsible for assisting in analyzing public policy developments, drafting responses to public policy, legislative and regulatory initiatives. Analyze regulatory frameworks in jurisdictions where the firm is or is considering carrying on business, preparing presentations relating to public policy, developing and operationalizing the firm’s South American strategy.
· Deepen the firm’s ...
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