.../ 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 device development projects in a global environment. You will be accountable for scope, budget, and timing, ensuring alignment with the Project Charter and business case while managing risks a...
.../manage improvement projects within the organization; (CAPA, VIP, QMP, StAR, Lean, 5S). Act as team/cross-functional team member/lead in supporting quality disciplines, decisions, and practices both i...
...Medical Translator/In-house Linguist (English to Japanese) Location: EMEA - Home-Based Unlock Your Potential with IQVIA Language Solutions! At IQVIA Language Solutions, we stand out as the only 100% l...
...other scientific fields including atmosphere/ocean sciences, computational life sciences, mathematical biology, mathematical economics, medical and seismic imaging, theoretical computer science, and t...
.../or Kaizen Strong communicator — you keep teams aligned and take others with you Proactive, energetic, and results-driven — you take initiative and follow through Strong communication skills; fluent i...
...health, and overall well-being. This includes retirement plans, health programs, life insurance, and comprehensive medical care. Work-Life Balance & Flexibility Maintain a healthy balance between work...
.../lean experience, managing large, multi-site project/programs within complex cross-functional organizations and/or environment with several disciplines Experience in medical device industry with an un...
...other COE stakeholders. Ensure the Total Rewards function continuously evolves its offerings to meet the changing needs of a high-growth, science-driven organization. Executive Compensation & Governan...
.../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...
...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...
...medical devices. Rich experience in the field of document reviews, CAPA and improvement projects Preferable experience in working in venture / start-up setups incl. basic business understanding Prefer...
.../ standard / guidance / cGMP and other local requirements together with other department. Maintain the validation master plan (VMP) and procedures, and ensure alignment with the company's quality mana...