10 product manager jobs found

Cambrex Manager, Analytical Services US-NC-Durham Job ID: 2026-5101 Type: Regular Full-Time # of Openings: 1 Category: Analytical Services Cambrex - Durham Overview Our Analytical Services Department is seeking a motivated analytical scientist at the Manager level to oversee a growing team of analytical scientists focused on supporting a wide range of clinical to commercial Quality Control and Analytical Development workflows for drug substance and drug product. Reporting to the Associate Director, the Analytical Services Manager will provide overall strategic oversight and operational direction for a highly cross-trained team of analytical scientists simultaneously supporting both development and quality control testing for small molecule drug substances and drug products in a fast-paced work environment. The Manager will be responsible for operational project planning including resource allocation, technical project oversight, quality oversight, and...

Cambrex Senior Scientist 2 – Engineering Research and Development (ERD) US-NC-High Point Job ID: 2026-4989 Type: Regular Full-Time Category: Research & Development Cambrex - High Point Overview Position is directed toward optimization of existing chemical routes and development of novel alternate chemistries/processes toward key synthetic intermediates and APIs. Provides CHP site engineering support, including the design, construction, and maintenance of equipment that replicates laboratory chemical process on pilot and commercial scales. Experimental skills related to chemical process development and kilo – scale synthesis of organic compounds of medicinal importance, including chemical synthesis and product isolation/purification. Utilizes analytical tools to assess product quality and process performance. Serve as an expert chemical engineering and pharmaceutical science resource to the chemical development group, the Cambrex High Point...

The Research Assistant II performs a primary research role in the laboratory and conducts original research for both internally and externally funded projects of interest to the laboratory. Assists with preparation of manuscripts and reports for the laboratory, oversees the day-to-day management of the project and coordinates sample and data collection. Supports the laboratory administratively by ordering and organizing lab stocks and supplies, maintaining safety records and assisting with the preparation of reports for regulatory groups (e.g. IRB, radiation safety), as they relate to the research project. Develops and maintains computerized record systems for the research project, which may require development of web-based forms and limited computer programming. Essential Functions: 1. Manage routine mouse colony and animal husbandry activities, including breeding, weaning, animal identification, colony census, cage-card and database maintenance, and coordination of...

Overview Lumicera Health Services is seeking a Sr. Manager, Industry Relations  to join our team!       The Sr. Manager, Industry Relations leads the team responsible for establishing, maintaining, and enhancing effective relationships with pharmaceutical manufacturers that produce specialty pharmaceuticals, and directs the negotiation of distribution and procurement contracts to ensure the specialty pharmacy can obtain specialty pharmaceuticals and pricing that meet the demands of its payers and patients. The primary responsibility of this position is to develop and execute manufacturer and trade engagement strategies, oversee the clinical drug pipeline, and maximize access to products in which the specialty pharmacy has a strategic interest in dispensing, including limited distribution medications. The Sr. Manager will lead and develop the Trade Relations team and Proposal Analysts and support Lumicera and its strategic partners in achieving business objectives and...

Overview Due to growth, we are adding a Supervisor, Specialty Pharmacy Support Services to our team .   Under general direction of the Associate Manager, Pharmacy Services, the Supervisor, Specialty Pharmacy Support Services is responsible for managing the day-to-day operations of a team of either Reimbursement or Intake Specialists. This position monitors productivity and performance standards and plans and directs workflow and project assignments. Oversees production volume to ensure service standards are met. The Supervisor, Specialty Pharmacy Support Services will participate in hiring, training, and evaluation of staff, as well as be responsible for team’s adherence to corporate attendance and employment policies. This individual will work with the Associate Mgr, Pharmacy Service to develop policies, procedures, and the business work plan for the team and recognize and recommend operational improvements. Lastly, the Supervisor will train staff and intervene to...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Siemens Healthineers' Radiopharma Solutions is a global leader in PET (Positron Emission Tomography) radiopharmaceutical manufacturing and distribution. With more than 47 locations worldwide, Radiopharma is the largest PET radiopharmaceutical network in the industry, supplying more than one million doses annually to over 2,800 imaging centers around the globe. Learn more about Radiopharma Solutions: https://www.siemens-healthineers.com/en-us/molecular-imaging/radiopharma New Job Description As a Nuclear Pharmacist, you will oversee the production, quality control, and dispensing of radiopharmaceuticals in...

Allucent Location: Cary, North Carolina, United States Department: Regulatory & Drug Development Consulting (RDC) Description At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. About the Role Bring your expertise in regulatory affairs and join Allucent as a Regulatory Affairs Scientist I or II to assist clients with regulatory affairs related activities for drug, biologic, or medical device products and serve on project teams in various capacities such as Subject matter Expert, Assistant Consulting Lead, and Consulting Lead. Your main responsibilities will include but not limited to: Prepare and review regulatory and scientific documents for drugs, biologics, or devices, ensuring accuracy, quality, and compliance across development and lifecycle stages. Support regulatory...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Siemens Healthineers' Radiopharma Solutions is a global leader in PET radiopharmaceutical manufacturing and distribution. For nearly three decades, Radiopharma has been a trusted partner in molecular imaging, delivering routine, reliable access to high-quality radiopharmaceuticals that support critical diagnostic procedures. With more than 47 locations worldwide, Radiopharma is the largest PET radiopharmaceutical network in the industry, supplying more than one million doses annually to over 2,800 imaging centers around the globe. Because we operate the industry's largest network of pharmacies, sites support...

The Provider Network Quality Assurance Specialist is responsible for monitoring, auditing, and improving the quality, accuracy, and compliance of provider network operations. The role supports provider data integrity, regulatory compliance, provider directory accuracy, and continuous process improvement. This position is fulltime remote. Selected candidate must reside in North Carolina. Some travel for onsite meetings to the Home office (Morrisville, NC) may be required.   Responsibilities & Duties Conduct Quality Audits of Provider Network Operations Processes Develop and maintain an audit schedule Conduct research, analyze data, and make recommendations regarding administrative, organizational, and operational problems Maintain audit evidence and records to support internal and external review readiness Support Provider Directory Accuracy and Provider Data Validation Initiatives Perform reviews of Provider Directory accuracy...

Are you motivated to participate in a dynamic, multi-tasking environment? Do you want to join a company that invests in its employees? Are you seeking a position where you can use your skills while continuing to be challenged and learn? Then we encourage you to dive deeper into this opportunity. We believe in career development and empowering our employees. Not only do we provide career coaches internally, but we offer many training opportunities to expand your knowledge base! We have highly competitive benefits with a variety HMO and PPO options. We have company 401k match along with an Employee Stock Purchase Program. We have tuition reimbursement, leadership development, and even start employees off with 16 days of paid time off plus holidays. We offer wellness courses and have highly engaged employee resource groups. Come join the Neo team and be part of our amazing World Class Culture! NeoGenomics is looking for a Molecular Operations Scientist who wants to learn to...