.../Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any oth...
.../ Raritan, NJ /Spring House, PA, US (Hybrid / 3 days onsite per week preferred) . Please note that this role is available across multiple countries and may be posted under different requisition number...
...medical contact for study teams, investigators, and internal/external stakeholders. Contribute to protocol development, study design, and medical monitoring plans. Assess reported safety events and ev...
.../office-based role within the ICON premises in Assen, Netherlands.What will you be doing as Quality Assurance Auditor?We are looking for you to join our team in Assen, the Netherlands where you will t...
.../manages improvement projects within the organization (VIP, QMP, Star, Lean, 5S). Understands and utilizes problem solving methodologies; (CAPA, Is/Is not diagram/Fishbone diagram, Pareto, FMEA). Acti...
.../ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to conta...
...medical technology company, is well-positioned to lead the way in today’s rapidly changing healthcare industry. With over $31 billion in revenue, we deliver exceptional results and innovative solution...
.../patient/ people-centric, self-motivated. A collaborative and highly structured strategic thinker who is driven for results, has excellent written and oral communication skills, is comfortable with un...
.../patient/ people-centric, self-motivated. A collaborative and highly structured strategic thinker who is driven for results, has excellent written and oral communication skills, is comfortable with un...
...other's work happiness. Here, we know each other by first name and strive for success together. Valued expertise: At Oliver, you have the freedom to apply and grow your technical insights daily. We va...
.../or procedures for regulated products /businesses. Have an impact on processes such as the introduction/validation of new/changed manufacturing processes and their associated Quality systems, the tren...
.../or procedures for regulated products /businesses. Have an impact on processes such as the introduction/validation of new/changed manufacturing processes and their associated Quality systems, the tren...
.../or procedures for regulated products /businesses. Have an impact on processes such as the introduction/validation of new/changed manufacturing processes and their associated Quality systems, the tren...
...Medical Devices Industry or equivalent. Extensive knowledge on (non-)Medical Device development standards (e.g. ISO13485) and regulations (e.g. 21CFR820, EU MDR) and FDA 510K Extensive experience with...
.../or global projects. Perform other duties as assigned. Preferred Requirements Previous office based experience is essential Excellent commercial skills Ability to understand and/or deploy key internal...