- CSL Behring (King Of Prussia, PA)
- …is accelerating innovation to deliver greater impact for patients. With a project -led structure and a focus on collaboration, we're building a future-ready team ... GRA. With support, engaging with health authority (HA) in stationed country ( FDA or EMA), maintaining productive relationship with HA contacts and driving positive… more
- Bausch + Lomb (Kirkwood, MO)
- …**Objective:** We are seeking a highly experienced and technically proficient Senior Manager to lead our Electronics Design Group within a surgical equipment R&D ... along with a thorough understanding of IEC 60601 standards, FDA and EU design control regulations, and risk management...device in emerging designs + Provide estimates of design project resource and time requirements and design path risks… more
- Wolters Kluwer (Waltham, MA)
- The **Principal SaMD Technical Program Manager ** plays a pivotal role in driving the development and delivery of Software as a Medical Device (SaMD) products. This ... ensuring strict compliance with global regulatory standards such as FDA , EU MDR, ISO 13485, and IEC 62304. They...dependencies. They provide oversight to various aspects of the project portfolio, coordinating meetings and project deliverable… more
- Medtronic (Fridley, MN)
- …throughout the project lifecycle + Medical device / regulated / FDA environment + Developed and implemented culture change + Excellent organizational skills ... stakeholder management and communications - effectively and efficiently communicating project status, priorities, risks, and issues to multiple stakeholders,… more
- Perdue Farms, Inc. (Accomac, VA)
- …thrive. **That's Perdue.** **Summary** We are actively recruiting for a strong FSQA Manager to provide leadership, direction and execution of all plant food safety ... Provide leadership and be an active member of all project teams to ensure food safety and quality concerns...working relationship and act as a plant liaison with FDA and USDA staff. + Develop staff through appropriate… more
- Insight Global (Memphis, TN)
- …client of Insight Global is seeking a Supplier Quality and Compliance Manager to lead supplier assessments, manage corrective actions, support new product ... focus on building strong supplier relationships and implementing performance metrics, the manager plays a key role in maintaining product integrity and operational… more
- Abbott (Des Plaines, IL)
- …medicines. Our 114,000 colleagues serve people in more than 160 countries. **Senior Manager Quality** **Working at Abbott** At Abbott, you can do work that matters, ... legacy of pioneering work in medical diagnostics. The position of **Senior Manager Quality** within our Molecular Diagnostics Business Unit located in **Des Plaines,… more
- Mount Sinai Health System (New York, NY)
- …This role ensures high-quality, efficient study execution consistent with institutional, FDA , and ICH/GCP standards. The Manager leads cross-functional study ... **Job Description** The **Clinical Trial Manager ** provides leadership and oversight for the planning,...degree or equivalent advanced training in clinical research or project management preferred. + 6+ years of experience managing… more
- W. R. Grace (Columbia, MD)
- Category Manager - Pharma Chemicals and CDMO Apply now " Date:Nov 20, 2025 Location: Columbia, MD, US, 21044 Company: W. R. Grace & Co. Annual Wage Range:$103,975.20 ... Columbia, MD and locations worldwide. Job Description The Category Manager - Pharma Chemicals and CDMO is responsible for...R&D, Quality, Regulatory, and Manufacturing to align sourcing with project needs. + Drive cost savings and value creation… more
- Hologic (Newark, DE)
- Sr Manager , Quality Assurance Newark, DE, United States Marlborough, MA, United States Are you a strategic leader with a passion for driving compliance, quality ... regulated environment? At Hologic, we are seeking a **Senior Manager , Quality Assurance** to lead the development, implementation, and...Systems (QMS) and electronic documentation systems. + Expertise in FDA 21 CFR Part 820, ISO 13485:2016, EU MDR… more