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

Pharmacy Technician Req # 0000131066 Category Pharmacy Status Per Diem Shift Day Facility Newark Beth Israel Medical Center Department Pharmacy Location Newark Beth Israel Medical Ctr, 201 LYONS AVENUE, NEWARK, NJ 07112 2027 Job Title Pharmacy Technician Location Newark Beth Israel Medical Center Req# 0000131066 Status Per Diem Shift Day Department name Pharmacy Job Overv

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

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

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

Job Title Associate Scientist II Job Id 24 01899 Location East Hanover, NJ Duration 05 Months On W2 Contract The role is to provide technical lab support to project managers. Familiarity with sample prep, bench based chemistry and measurement techniques, data collection and data management. Experience working in a lab environment is a must. We are looking for a candidate

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

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

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

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

Rutgers, The State University of New Jersey is seeking a Postdoctoral Fellow for the Department of Microbiology, Biochemistry and Molecular Genetics within the New Jersey Medical School. Our goal is to characterize putative ER shaping proteins of Plasmodium, their functions in the parasite's cell biology and their effect on parasite virulence. We use tools of molecular ge

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

Prepares medication orders by compounding or admixing medications under supervision of a registered pharmacist. Checks all orders for completeness of information. Verifies patient information and proper physician authorization. Checks all orders for insurance approval before admixing. Under a professional's supervision, admixes drugs as ordered by physician in an accurate

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