Senior Associate Director - Pharmaceutical Development - Rockville, MD - beBeeProductQuality

+ Job summary: ProSidian Seeks a Senior Pharmaceutical Business Development and Portfolio Management SME | Healthcare and Life Sciences [HHS119024]. · Responsibilities:Support BARDA Program Office(s) as a subject matter expert in the fields of Chemical Threats, Radiological/Nucle ...

The Senior Digital Standards and Industry Solutions Manager will be the intrapreneurial, market-creating lead for USP's efforts to drive industry adoption of digital standards in drug development and regulatory submissions. · This role is remote with an expected travel commitment ...

The Executive Director Corporate Development role requires a high aptitude in leadership product development market analysis commercial assessments intellectual property project management portfolio management data analysis process improvement financial valuations due diligence b ...

The Scientist of Drug Metabolism and Pharmacokinetics (DMPK) supports Supernus' drug discovery and preclinical development efforts in the department of Preclinical DMPK and Pharmacology. · ...

The Senior Digital Standards and Industry Solutions Manager will be the intrapreneurial, market-creating lead for USP's efforts to drive industry adoption of digital standards in drug development and regulatory submissions. · ...

USP is seeking a Senior Technical Advisor to expand competencies and capabilities in medical products manufacturing. · The incumbent will play a critical role in advancing formulation technologies to enable local manufacturing of high-quality medicines in LMICs.Provide technical ...

The Senior Digital Standards and Industry Solutions Manager will be the intrapreneurial, market-creating lead for USP's efforts to drive industry adoption of digital standards in drug development and regulatory submissions. As a strategic leader within the newly formed Digital St ...

The Associate Director, · Medical Affairs - ADHD will be the scientific expert involved in executing data generation and medical communication strategy.This position will work closely with Medical Director, · ADHD and will have primary responsibility for post hoc data-analyses, · ...

The Manager of Regulatory Affairs, Advertising and Promotion, is responsible for representing the Regulatory Affairs department at Promotional and Medical Review Committee meetings ensuring alignment with promotional strategies and regulatory expectations. · ...

We are seeking a motivated Validation Intern to support our validation team in delivering high-quality services to clients in the pharmaceutical and biotech industries. · This internship offers hands-on experience with equipment qualification, system validation, and documentation ...

The USP is seeking a Senior Digital Standards Policy and Implementation Manager to lead the development of internal and external policy frameworks that support the creation, · governance, · and regulatory adoption of Digital Standards. · ...

The Director, Medical Communications leads the medical affairs function of scientific content development of product- and disease related materials.Develops and reviews medical affairs materials to ensure a balanced view of all available product information. · Serves as a medical ...

The Senior Manager Clinical Research is a key position at Supernus Pharmaceuticals, · Inc. · This role involves leading/co-leading clinical research activities in support of three key initiatives: Clinical research supporting activities within the Clinical Development Group (phas ...

This Associate Principal Scientist in Pre-approval Pharmaceutical CMC will be responsible for developing and implementing CMC regulatory strategies. · This role supports respiratory/inhalation and some conventional small molecule programs. ...

The Supply Chain Quality Senior Manager will support pharmaceutical distribution activities for prescription drug products. · ...

The Director, Medical Communications leads the medical affairs function of scientific content development of product- and disease related materials. · Develops and reviews medical affairs materials to ensure a balanced view of all available product information. · Serves as a medi ...

The Senior Process Engineer is responsible for supporting the Technical Operations department through process development, optimization, and technology transfer activities. · This role performs a broad range of functions including designing and conducting experiments, · authoring ...

The Director of Technical Operations is responsible for providing scientific and technical leadership for the Technical Operations team. · ...

We are seeking a proactive and detail-oriented Contract Associate to support the CMC Team in executing key CMC activities with a focus on analytical development project management and clinical supply coordination.This temporary role is critical in ensuring that analytical strateg ...

· Develop internal policy frameworks for the creation,governance,and lifecycle management of USP Digital Standards. · ...

The Sales Training & Development Administrator supports the Sales Training & Development Team by coordinating and executing Sales Training and Sales Leadership Development initiatives across the sales organization. · This role will be responsible for the planning, implementation, ...