Biotech Jobs in South Plainfield, New Jersey

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188 South Plainfield, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 188
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...
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...
A leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world is seeking a qualified Chemistry Data Reviewer. Qualified candidate will review raw data in support of GMP testing. Bachelor's degree with 2+ years of the following experience required: -Analytical Chemistry required. -GMP experience required. -Experience ...
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...
Appco Pharma is focused on developing, manufacturing and distribution of Generic & Prescription Pharmaceutical products in multi-product oral dosage forms to customers throughout the United States. Appco Phama is looking for CEO who will report directly to the chairman of the Appco Pharma. Roles & Responsibilities 1) Provide strategic leadership to the company and direct the Executive Managemen...
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. Group Director, R&D, Applied Science and Technology-1218140731 Description Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Group Director, R&D, Applied Science and Technology (AST) to be located in Somerville, New Jersey. The Ethicon business offers a broad range of products, platforms and ...
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...
Provide statistical programming expertise in SAS for the production of analyses, tabulations, graphics, and listings from clinical trial data. Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports. Contribute to the integr...
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 Director, Global Project Leader, Instruments; this position will be located in Raritan, NJ. Ortho Clinical Diagnostics, Inc. (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 ...
Ortho-Clinical Diagnostics is recruiting for Project Managers in our R&D Department and these positions can be located in either Raritan, NJ or Rochester, NY. Ortho Clinical Diagnostics (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approx...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Regulatory Program Management-5590140917 Description Janssen Research and Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Regulatory Program Management to be located in Raritan, NJ; Titusville, NJ; or Spring House, PA. Janssen Research & Development, ...

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