Staff Regulatory Affairs Specialist

**Job Description Summary** The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product development. The incumbent will...

Job Description Summary Drive the Cost to Win process for the IS/CC platform; including but not limited to maintaining visibility to GP goals costs targets, providing leadership and support to drive ideation, feasibility & project execution to deliver platform cost to win savings. Facilitates business and plant teams to maintain progress on successfully...

Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech...

We are a team of specialists serving real estate buyers, sellers, and investors in the area. We're looking for a Showing Agent to support sales goals through effective sales techniques and quality customer service.GOALS: Create/Convert/Close, 20 approved buyers working at all times, 50 showings per week to fully qualified buyers, an average of 5 homes shown...

The Specialist, Medical Affairs for Post-Market Surveillance (SMA-PMS) for Specimen Management (SM), Medical Affairs (SA) is responsible for post-market reporting compliance activities. This position is accountable for coordinating and contributing t Medical, Specialist, Quality Assurance, Technical, Regulatory Affairs, Project Management, Manufacturing,...

DemeTECH is seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory guidance, and managing...

DemeTECH is seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory guidance, and managing...

DemeTECH is seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory guidance, and managing...

DemeTECH is seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory guidance, and managing...

Job DescriptionJob DescriptionWe are seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory...

Job DescriptionJob DescriptionWe are seeking a highly motivated and detail-oriented Sr. Regulatory Affairs Specialist to join our team. The ideal candidate will play a pivotal role in ensuring our products meet all regulatory standards and achieve timely market access. This role involves collaboration across various departments, providing regulatory...

Title: Regulatory Affairs Mfg Consultant Location: Franklin Lakes, NJ Contract Term: 7+ Months Shift/Hours: 1st Shift ( 8-9am to 4-5pm) / 40hrs Client: Medical Device Company Job Category: Regulatory Affairs / Compliance Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1Bs Job Description: This position is responsible for the...

Title: Regulatory Affairs Mfg Consultant Location: Franklin Lakes, NJ Contract Term: 7+ Months Shift/Hours: 1st Shift ( 8-9am to 4-5pm) / 40hrs Client: Medical Device Company Job Category: Regulatory Affairs / Compliance Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1Bs Job Description: This position is responsible for the...

Description We are the makers of possible  BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

Education or Equivalent Requirements:Bachelor’s degree in a life science or related field preferredMinimum 5 years of experience in Regulatory Affairs, Quality Assurance or related field or any combinationExperience working in a manufacturing, pharmaceutical and/or GMP facilityMust be detail oriented with well-developed analytical skills.Ability to...

COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE! Hybrid work arrangement Medical, Dental, Vision Benefits Health Savings Account (HSA), Flexible Spending Account (FSA) Prescription Drug Coverage Telehealth and Behavior Health Services Income Protection – Short Term and Long Term Disability Benefits Retirement Benefits - 401k Company Match on...

Job Description:This Regulatory Affairs Scientist position in Mars Pet Nutrition provides nutrition and regulatory guidance in a rapid changing environment to support strategic and innovative Mars business priorities. This fast paced and exciting position has exposure to many parts of the business and works cross-functionally with the eCommerce, Legal,...

Job Description:This Regulatory Affairs Scientist position in Mars Pet Nutrition provides nutrition and regulatory guidance in a rapid changing environment to support strategic and innovative Mars business priorities.  This fast paced and exciting position has exposure to many parts of the business and works cross-functionally with the eCommerce, Legal,...

Position : Senior Manager, EU MDR/IVDR Location : Franklin Lakes, NJ Duration : 12 Months Contract Total Hours/week :40.00 Description: The Senior Manager, EU MDR/IVDR, Medical Governance and Analytics, will drive strategy for managing the Medical Affairs approach to compliance with EU MDR/IVDR including creating department policies, procedures and work...

The R&D Staff Packaging Engineer will impact health care and the MDS business groups by driving commercialization of new products and design changes for current products through development, qualification and launch phases.The R&D Staff Packaging Engineer contributes to building organizational effectiveness through creating, using and sharing standard...

Position: Clinical Lab SpecialistLocation: Franklin Lakes, NJ 07417Duration: 12 Months contract with possible extensionPay Rate: $40/hr - $47/hr (depending on experience)Job Description:On Site in Flks 5 days WEEK 8:30 TO 5:00Working with Human BloodShould either have ASCP generalist certification OR eligible to receive one.This laboratory-based position...

Position: Clinical Lab SpecialistLocation: Franklin Lakes, NJ 07417Duration: 12 Months contract with possible extensionPay Rate: $40/hr - $47/hr (depending on experience)Job Description:On Site in Flks 5 days WEEK 8:30 TO 5:00Working with Human BloodShould either have ASCP generalist certification OR eligible to receive one.This laboratory-based position...

SummaryOur client, a global medical device & diagnostic manufacturer has engaged GForce Life Sciences to identify a hands-on Clinical Project Leader (CPL) to join and own the overall responsibility to define and implement the safety and efficacy (S&E) requirements for a new product. The position is also responsible for designing and interpreting results of...

SummaryOur client, a global medical device & diagnostic manufacturer has engaged GForce Life Sciences to identify a hands-on Clinical Project Leader (CPL) to join and own the overall responsibility to define and implement the safety and efficacy (S&E) requirements for a new product. The position is also responsible for designing and interpreting results of...