- Merck (Upper Gwynedd, PA)
- …create breakthrough science that radically changes the way we approach serious diseases. The Senior Director will report to an Associate Vice President in the ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Responsibilities:** Specifically, the Senior… more
- Pfizer (Rocky Mount, NC)
- …to improve manufacturing success rates and ensuring zero down time. As a Sr . Automation Engineer your knowledge and skills will contribute towards the goals and ... more than 0+ years of experience; + OR an associate 's degree with 6 years of experience; OR a...addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0%… more
- Boehringer Ingelheim (Ridgefield, CT)
- …development projects, reporting to the Associate Global Head or the Global Clinical Programme Team Leader. The Senior Clinical Program Leader has a ... **Description** The Senior Clinical Program Leader assumes global ...for continuous benefit-risk assessment. + Provides medical leadership in regulatory meetings and contributes to submission strategy, regulatory… more
- Lilly (Indianapolis, IN)
- …of new sites, and assisting in the maintenance optimization efforts for existing global sites. The Associate Director will oversee the business side, support ... optimized for global operations. + Ensure the systems' compliance with regulatory requirements and GQS standards. + Maintain data integrity within the systems,… more
- Lilly (Pleasant Prairie, WI)
- …and Site Goals. + Establish a laboratory operation compliant with Lilly Global Quality Standards and regulatory requirements through development of effective ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...and new state of the art QC laboratories. The Associate Director, Quality Control (QC) - Chemistry, is responsible… more
- Zimmer Biomet (Englewood, CO)
- …in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced ... competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating...Paragon 28, a Zimmer Biomet company, is hiring an ** Associate Quality Engineer - Design** to support our fast-moving… more
- Wolters Kluwer (Waltham, MA)
- Wolters Kluwer is a global leader in professional information services that combines deep domain knowledge with specialized technology. Our portfolio offers software ... to help save lives, improve the way we do business, build better judicial and regulatory systems. We help them get it right. **Who We Are:** Wolters Kluwer: The… more
- BeOne Medicines (Emeryville, CA)
- …+ Contribute to internal presentations, dashboards, and data summaries for senior leadership and regulatory submissions. + Implement process improvements ... Reporting to the Head/Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial diversity strategy through… more
- AbbVie (North Chicago, IL)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues.… more
- System One (Lakewood, CO)
- …+ Interpret and implement FDA, GMP, GDP, ISO, ASTM, EMEA, and other global regulatory requirements. + Ensure compliance with company Quality System regulations ... Job Title: Senior Manager, Engineering Plastics Processing Location: Onsite- Lakewood,...long term planning. + Broad theoretical knowledge of quality, global regulatory standards, management, and manufacturing. +… more