R & D Jobs in Mahwah, New Jersey

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61 Mahwah, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 61
Regulatory Documentation Coordinator You're precision-oriented and a stickler for doing it right. You have deep expertise in pharmaceutical compliance and quality control. Your critical thinking prowess makes you a problem solver extraordinaire. You generate powerful ideas and know how to get them implemented. If this describes you, this opportunity from Experis is just right for you. ***This is...
Manager, Regulatory Affairs Location: Mahwah, NJ The Manager, Regulatory Affairs works with a high level of autonomy to bring medical devices to market and ensure ongoing compliance while managing a regulatory team. They are responsible for providing their team with ongoing developmental opportunities, supporting team building activities, and promoting a healthy work/life balance. They participa...
Associate Manager, Regulatory Affairs Location: Mahwah, NJ Minimum Qualifications: • Bachelor’s Degree in Engineering, Life Science or other related scientific area. Prefer Advanced degree and/or RAC certification. • 5 years’ experience within medical device industry. Prefer Cross-functional experience in Product Development, Quality Engineering, Legal, Intellectual Property, and Advanced Tech...
Our client, a large pharmaceutical company, is currently seeking a QC SCIENTIST. This includes the testing of all active substances, raw materials (excipients) and finished dosage forms. - Individual will provide training to other individuals. Individual is capable of independently troubleshooting analytical and instrument problems. - Individual is also responsible for assuring adherence to Fed...
Formula Scale-Up Specialist: We have a permanent opportunity with our very stable client in Mahwah, NJ. Please review the following description and submit your resume if you are the right fit! Position Duties/Responsibilities: Interfacing with clients from development to commercial production stages Formulation/Process scale-up experience Creation of batch records Protocol creation Validati...
Currently we have a temporary opening for Cell Therapy Scientist to support a company located in the Ramsey, NJ area.   Responsibilities: Process, cryopreserve, and otherwise manipulate cell products using sterile techniques, according to written Standard Operating Procedures, in accordance to facility cGMP practices. Operate equipment according to designed procedures. Could include but is not...
Currently we have a temporary opening for a MSDS Author and Labeling Specialist to support a company located in the Ramsey, NJ area. Responsibilities: Assist in the creation of MSDSs and labels, and the day to day management of SAP database (data input, search, publishing) and daily regulatory product safety functions including: Perform GHS Classification of Mixtures and Substances required for...
Lead Technical Process This position carries the responsibility for the direct client interface during the development, scale-up, transfer, and /or commercialization of products. This includes batch record creation, review, generation of DOE and sampling protocols, validation documents, authorship of final reports and technical project guidance to the client. This position is also accountable fo...
Summary Our client is a leading global medical device manufacturer Client Details Our client is a leading global medical device manufacturer Description The Supply Planner & Process Improvement Specialist will be responsible for all demand, supply, inventory, and SC project planning activities for your product/customer portfolio. This individual works closely with Customer Operations to ensur...
Job Number: 424132 Senior Biostat SAS Programmer Analyst OVERVIEW Expert in addressing technical challenges that connect SAS, CDISC and XML. Excellent technical skills in SAS system and application development. Proven experience in development and implementation of clinical standards in a global pharmaceutical environment. Expert in integrating SAS with other leading technologies such as PDF...
Job Number: 423911 Biostatistician DESCRIPTION OF JOB: Commercial Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management...
Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Work with the clinical study team on study design, developme...
TechData is hiring for Associate Director of Biostatistics (Prefer Bayesian adaptive designs),SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some can be telecommuting), Medical Writer, Regulatory Documentation Specialist, Senior Publishing Specialist, Sr. Clinical Supply Manager, Sr. Clinical Data Manager for our pharmaceutical clients in Northern NJ. We also have...
Quality Control Supervisor Job Label:CMI_QCS We have an opportunity for a Quality Control Supervisor to join our growing team. Collagen Matrix, Inc., located in Oakland, NJ, is a leader in the design and engineering of collagen and mineral-based extracellular matrices for tissue and organ repair and regeneration. The Company currently manufactures collagen and mineral-based finished medical devi...
Qualifications: 1. History of success designing disposable medical instrumentation 2. Working knowledge of plastics and injection molding processes 3. Knowledge of GDT and ability to perform complex tolerance stacks 4. Expert in mechanism design (actuators, gears, levers, buttons, etc) Responsibilities: The candidate will contribute to the design and development of medical devices...
Small flavor company looking for person to lead quality control and regulatory department . Ideal candidate will have minimum of ten years experience working in the flavor and fragrance industry . Responsibilities will include all specification sheets , certificates of analysis , MSDS sheets , and related documents .In addition should have experience with the following - organoleptic analysis, spe...
Company: Yoh Clinical Outsourcing Manager needed for a contract opportunity with Yoh's client located in Woodcliff Lake, NJ. What You'll Be Doing: - Support internal customers in the development of outsourcing requirements for Phase I-IV global clinical trials. - Lead and support the qualification and evaluation process for new service providers. - Lead the process of Request for Proposal (RF...
This pharmaceutical company is known as a human health care (hhc) company seeking innovative solutions in disease prevention, treatment and care for the health and well-being of people worldwide. They use their talents to explore new therapeutic approaches that help address two key goals: meeting the medical needs of patients and their families, and improving their quality of life. Responsibiliti...
Join Fortune 100 company with top benefits and growth! The ideal candidate for the Senior Manager – Forensic Services role will identify, direct, plan, coordinate and perform proactive / reactive audit and investigative procedures related to associated risks and allegations of potential violations of company policies and/or other applicable laws for company in accordance with established procedur...
CHEMIST – Temp to Perm!!!!! Function: Test raw materials, in-process, prototype formulation drug products, finished products submitted and/or produced by the Formulation/Development Lab and Contract Manufacturing using USP/NF, EP, JP, client specific or other compendial methods. Participate in the method transfer and method development activities as dictated by the project scope of the Analytical...

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