R & D Jobs in South Plainfield, New Jersey

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217 South Plainfield, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 217
GENEWIZ, Inc. is a leading global genomics service company. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, next generation sequencing, bioinformatics, and GLP regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effective manner through specialized expertise and customizable, scala...
One of the world’s leading chemical companies has a job opening in their central New Jersey location. The company seeks a research engineer with a degree in Chemistry or Chemical Engineering to work on experimentation related to catalysts that reduce harmful emission gases. The company designs and develops catalysts and adsorbents used to treat and purify emission gases from power plants, or from...
TechLaw, Inc., a nationwide Environmental Consulting firm, seeks chemists and biologists of all levels for Environmental Services Assistance Team contract supporting U.S. EPA laboratories located in Edison, NJ. Experience with organic and inorganic laboratory equipment, laboratory procedures, sample extractions, and EPA analytical methods are desired. Candidates must have at least a BA/BS degree...
This a terrific opportunity for an Investigation Associate with a niche generic pharmaceutical company engaged in the manufacturing of multi-source and branded pharmaceuticals for pain management and anesthesia in the United States and across the globe. This ever growing company is looking for an Investigation Associate to come on board to their NJ facility. SUMMARY: Reviews, coordinates, and as...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fifteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: The QCCM, under the supervision of the Associate Director of Quality Systems andRegu...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fourteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: Under the direct supervision of the Supervisor, Quality Control Laboratory, the inc...
Growing Pharmaceutical client in Central/Northern NJ area is looking to fill a temp-to-perm role for a Director, Quality Assurance/Auditing with large molecule, biologic experience. This job will have the following responsibilities: ·Manufacturing is done on-site, so client needs a hands-on leader to oversee QA and internal audit compliance. ·Primarily GMP, but some GLP and GCP oversight as wel...
· High school diploma or general education degree (GED) is required; and one year related experience in QA Inspection; or combination of education and experience. · Ability to read and comprehend simple instructions, short correspondence, and memos in English. · Ability to speak effectively in English in one on one or small groups. · Ability to add, subtract, multiply, and divide in all units o...
The Quality Assurance department plays a critical role in the daily operations of the facility. The primary function of the department is to ensure compliance with c-GMP, domestic and international, as well as direction and oversight of internal quality systems requirements for the facility. The department is entirely separate from and independent of the personnel engaged in the direction and cond...
Works with guidance from senior staff members develops formulations for a variety of dosage and delivery forms that support new products or product/process optimization projects. Prepares stability, consumer, and clinical samples as needed. With minimal supervision, run and monitor benchtop, pilot, and manufacturing scale-up and verification batches. Require Hands on experience or knowledge to o...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
Johnson & Johnson companies are equal opportunity employers. Staff R&D Engineer-9583140428 Description Mentor, a member of Johnson & Johnson's Family of Companies is currently recruiting for a Staff R&D Engineer, to be located in Somerville, New Jersey. Mentor Worldwide L.L.C., is a trusted global leader in aesthetic medicine among both consumers and clinicians by providing a broad range of in...
Auditor Principal Specialist GCP Requirements: - Bachelor degree preferably in a life / medical / natural sciences or scientific discipline - 10 to 14 years of pharmaceutical (or related) experience with BA or 8 to 12 years with advanced degree, e.g. MBA, MS, PharmD, PhD. This includes a minimum of 6 years of Clinical Quality Assurance related experience and/or experience in Clinical Trials suc...
Product Complaint Associate JOB SUMMARY: The Product Complaints Associate will manage the administration of the Clinical and Commercial Complaints systems including the receipt, coordination of returns, investigation and final correspondence of all Product Complaints for Global Products. This role will drive the Investigation process for QA with emphasis on compliance to SOPs and applicable Regu...
Job Title: CMC Sr. Manager Location: Bridgewater, NJ Duration: through 3/22/2015 Skills: - BA/BS in a science/health field (eg, Chemistry, Pharmacy, Biology) plus 7 yr industrial experience (chemical, analytical, pharmaceutical, manufacturing) including 4 yr in regulatory CMC or advanced degree (MS/MA, PhD) in a science/health field plus 4 yr industrial experience including 2 yr in regulatory ...
Job Number: 423676 SAS Programmer II OVERVIEW Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in ...
TechData is looking for Biostatistician (some can be telecommuting), SAS Programmer/Statistical Programmer (Some can be telecommuting), Recruiter, Project manager, Quality Assurance, Database Administrator, Drug Safety Specialist, Clinical Data Managerfor our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: *****. TechData is a l...
2 openings follow AVP of Marketing reports to VP of Marketing. VP of Marketing reports to VP/Head of Commercial Strategy & Operations. AVP will manage 5 groups with 5 direct reports. VP has 8 direct reports + 5 that report to AVP. The entire team is about 34. Benefits - Full Relocation Assistance Available - Yes Bonus Eligible - Yes Interview Travel Reimbursed - Yes AVP Evidence Lead Diabete...
Ortho-Clinical Diagnostics is recruiting for a Manager, Worldwide Commercial Enablement, which is part of our Commercial Operations, and can be located off or on site, Rochester or NJ would be preferred. Ortho Clinical Diagnostics (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring an...
Ortho-Clinical Diagnostics, Inc. (OCD) is a leading provider of in vitro diagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around the world serving the global clinical laboratory and transfusion medicine community, and is committed to providing custom...

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