The Senior Director, Medical Affairs, Parenteral Nutrition (PN) is a critical role as this individual serves as the lead for the US PN Medical Affairs team and is responsible for developing and executing the US Medical Affairs strategy. This individual also collaborates closely with the Global business unit (BU) and the regional marketing organization to identify US nutri

The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for

include but are not limited to Provides development portfolio & program management to cross functional, cross divisional teams to drive execution and delivery in early to late phase complex development management programs to meet company strategic objectives. Actively manages cross program interdependencies and trade offs to ensure multiple programs are executed to predict

The primary responsibility of this position is to provide guidance to MSLs in cultivating current and future thought leaders in academic and clinical medicine at the local, regional, and national levels in the field of Hematology Oncology. The MSL Associate Director will lead, manage, coach, train, and develop MSL direct reports to support high performance, and to align w

Create and approve regulatory content documents that drive artwork and labeling language Review and approve final artwork Manage preparation of regulatory documents for new product launches and maintenance of current products in the market with the correct alignment and compliance to regulations Maintain required regulatory compliance databases, systems and processes Supp

We exist to help people thrive. Advancing health and nutrition is what we do best and care about.

Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, GSK House, Rockville Biopharm, Stevenage, UK Hertfordshire Ware, Waltham, Zug House Posted Date Feb 22 2024 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportuni

Responsibilities Essential Duties Follows established procedures and guidelines to manufacture the organization's products according to production specifications and schedules, volume, cost, and wastage targets or quality standards. Operates machines and production equipment safely and in accordance with instructions. Monitors the quality of output to identify, discard or

Contribute to lab scale process development to implement upstream discovery of flavor and modulation ingredients through microbial fermentation and biocatalysis Design and conduct microbial strain screening. Conduct instrumental analysis (GC MS & HPLC) of flavor components in samples to establish an in depth knowledge of flavor chemistry, pathways and molecular mechanisms

This individual will require an understanding of the scope of Medical Affairs training and excellence as well as excellent organizational and project management skills. The position will deliver by building strong relationships with key partners in a highly matrixed team environment. This role is accountable for executing the US Medical Affairs (USMA) training objectives,

PHARMACY TECHNICIAN MID SHIFT Job Locations US PA BETHLEHEM ID 2024 143339 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Join our PharMerica team! PharMerica is a closed door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long term care and senior living clients. We offer a non retail pharmacy environment.

At IPS, we apply our knowledge, skills, and passion to make a difference in the lives of people, solving complex challenges related to life sciences. We are looking for a dedicated Validation Engineer/Specialist to join our talented team at our office located in Somerset, New Jersey . In this role, you will perform cGMP compliance based services (commissioning, qualificat

Site Name UK Hertfordshire Ware RD, Durham Blackwell Street, GSK House, USA Pennsylvania Upper Providence Posted Date May 2 2024 As Regulatory Manager for devices, you will manage the overall global regulatory and advocacy strategy for GSK's portfolio of combination product devices (injectable and inhalation) across modalities and lifecycle We create a place where people

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. This position will serve as a technology partner in the Research and Development (R&D) and Technology Development & Operations (TD&O) domains, providing technology leadership, operational support and project management fo

We are looking to fill a Scientist 1, 2, or 3 position working as a full time employee of Parexel FSP on assignment onsite at one of our clients located in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer sponsorship. Responsibilities Build and maintain laboratory chemical collections according