About Sony Music Entertainment At Sony Music Entertainment, we fuel the creative journey. We've played a pioneering role in music history, from the first ever music label to the invention of the flat disc record. We've nurtured some of music's most iconic artists and produced some of the most influential recordings of all time. Today, we work in more than 70 countries, su

In this role, you will apply Biophysical analytical skills in biotherapeutic drug products characterization with focus on product robustness. You will be working in a collaboratively team environment to support both early and late stage formulation development. Responsibilities include Execution of testing protocols, including timely sample preparation, analytical testing

JOb Title Associate Scientist. Job Id 24 02124 Location East Hanover,NJ Duration 12 Months on W2 Contract Bachelor of Science Degree in relavent field. 2 years of analytical analysis experience preferred. Working as part of a project team, you support the delivery of long term research projects in line with the business and consumer needs. You plan and execute projects fr

The Thought Leader Liaison (TLL) is responsible for developing, managing, and engaging with Key Opinion Leaders throughout their assigned geography reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing. He/she works closely with commercial colleagues and other staff to help build advocacy of Mallinckrodt's products with KOLs. TheThough

In line with our mission, Bayer: Science for A Better Life we aim to improve quality of life.

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

The Associate Director, Regulatory Affairs CMC will be responsible for leading global regulatory CMC strategy for product development and registration, and for preparation of CMC dossier for primarily small molecule regulatory submissions (INDs and NDAs) according to global regulatory expectations and requirements. This position works cross functionally with Regulatory Af

A day in the life of a Start Up Specialist at Hackensack Meridian Health includes Manages all administrative/regulatory activities associated with start up of Oncology research trials conducted at JTCC including federal, pharmaceutical funded protocols and Investigator Initiated Sponsored Trials as assigned. Facilitates the Review and Execution of Confidentiality Agreemen

Under supervision, performs laboratory analyses of raw materials, in process (IP), finished products (FP) and stability (ST) samples for pilot and submission batches, according to SOPs and cGMP procedures. Prepares method validation protocols/reports, and carries out method validation activities, including interim method validation, to meet project timelines. Supports lab

This position is responsible to implement and manage the company's regulatory affairs function. Oversee and manage ongoing relationships with regulatory authorities. Responsibilities include the development, implementation and management of the Company's compliance functions. Responsible to ensure general compliance with Federal, and State regulations applicable to the di

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

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

CUSTOMER SERVICE PHARMACY TECHNICIAN Job Locations US NY UNIONDALE ID 2024 143051 Line of Business PharMerica Position Type Full Time Pay Min USD $18.00/Hr. Pay Max USD $19.25/Hr. Our Company PharMerica Overview harMerica is seeking a highly capable and motivated individual to join our team. PharMerica is a non retail pharmacy that focuses on providing exceptional custome

The specialist is expected to K now all brand submission requirements ; attend and complete any required brand specific training and credentialing need to service client work Partner with copy, project management, scientific strategy, editorial, and account team members for submission day success T ag, l ink , and u plo ad submission files and support materials , includin

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovativ