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

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

The Clinical Research Technician position is based within our Clinical Photobiology department, and works with departmental management and the Principal Investigator in the implementation of Photobiology trials. Job Type Full Time. Base Hours 9 00AM 6 00PM OR 10 30AM – 7 30PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual

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. In this role, you will perform cGMP compliance based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. Additionally, you will follow IPS an

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

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

Independently implement wide range of data analyses by using R or SAS. Data analyses may include regression analyses, survival analyses, parametric and non parametric testing, data visualization, simulations as well as advanced statistical methods such as propensity score matching, longitudinal data analyses, etc. Lead the drafting of statistical analysis plans and statis

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

Tris Pharma, Inc. (www.trispharma.com) is a leading privately owned biopharmaceutical company in the U.S. with a focus on development and commercialization of innovative medicines that address unmet patient needs. We have more than 150 US and International patents including applications and have marketed several branded and generic products in the U.S., have licensed our

Support and maintains clinical data management processes and data capturing systems for clinical trials by following Ferring SOP Support CRFs development, data mapping specifications, DVP, DMP, and data transfer specifications and tests EDC system functionalities. Participates in cross functional clinical trial teams and communicates data management matters effectively. T

Position Title Principal Scientist, Cognitive Sensory Sciences, L'Oreal Research & Innovation Location Clark, New Jersey (Hybrid) Department Evaluation Intelligence Are you obsessed about human senses, emotions, and cognitive understanding? Are you curious about the science behind the product and the impact on the consumer's senses and emotions? Are you a creative, inspir

Advance innovative technologies that transform sustainable raw materials to high value ingredients that modulate tastes and enhance authentic flavors through microbial fermentation and biocatalysts. Design and conduct lab scale process development to implement upstream discovery into pipeline. Conduct instrumental analysis (GC MS & HPLC) of flavor components in samples to

Manager, Regulatory Affairs North America (Hybrid) It's an exciting time to be part of IFF's Global Regulatory Affairs. This hybrid role requires presence in the office minimum of 1 day/week in the Holmdel, NJ location. As the Manager of Regulatory Affairs, you will be responsible for the regulatory compliance and conformity to customer requirements for fragrance products

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

Our Pharmacometricians are responsible for supporting quantitative decision making in drug development through the development and application of population PK, PK/PD, exposure response and other models. Qualified candidates will have the ability to work on a variety of therapeutic indications and data types and must be experts in applied Population PK, PK/PD, and/or expo