Biotech Quality System Consultant Jobs in New Jersey

Currently, there are no Biotech Quality System Consultant jobs available in New Jersey which match this search. You may wish to explore similar job titles on the Biotech jobs in New Jersey page or view related jobs below.
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Clinical Research Leader (Oncology); Highly Reputable Global Biotech, NJ Summary: Our client is a highly successful biotech company touted for its robust and diverse oncology portfolio of both marketed and investigational drugs. They are looking to hire a dynamic clinical research industry professional with experience managing all aspects of global oncology programs. This is an exciting and chall...
Main responsibilities Review and approve Raw material specifications and Product specifications Review and approve Raw Material and Product COAs Review and approval of laboratory equipment qualification documents B.S. in Chemistry preferred Experience in laboratory equipment qualification, laboratory investigations and deviation. Experience in RMS a plus Additional Responsibilities Manage ...
QA Consultant to work in R&D to do equipment qualification Main responsibilities · Review and approve Raw material specifications and Product specifications · Review and approve Raw Material and Product COAs · Review and approval of laboratory equipment qualification documents. Additional Responsibilities · Manage Laboratory Investigation Report (LIR) tracking system · Develop LIR metrics r...
GLOBAL CLINICAL PROTOCOL MANAGER - LATE PHASE SPONSORED RESEARCH WITH ONCOLOGY REQUIREMENT #14-00927 RECRUITER: CINDI PISNOY JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 2, 2014 Expected Areas of Competence: General · Manages successful execution and completion of assigned global clinical Phase IIIb/IV publication/medical informing trials within CSR&O Late Phase Sponsored Research unit, in adhere...
To maintain and coordinate Quality Systems related documents namely deviation reports, change controls and product complaints for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in analytical methods, test specifications and batch records. To issue effective documents including procedures, forms, report...
Are you looking for a Clinical Research position with a large pharmaceutical company? TechData Service has multiple positions open with many top pharmaceutical companies for positions including Project Manager with quality systems experience, Drug Safety Coordinator, Pharmacovigilence Scientist, Clinical Operations Manager/Project Manager, Scientist, Medical Information Specialist, CRA Monitor, C...
Joulé Scientific Staffing has an opening for a contract Quality Assurance Associate at a pharmaceutical company in the Princeton, NJ area. Job requirements: B.S., in Chemistry, Chemical Engineering, Biochemistry or related discipline, or its equivalent. 5+ years of relevant experience in a regulated environment with at least 2 years focused on product quality. Knowledge of biotech bulk and fin...
TechData is looking forBiostatistician (Some positions are remote), Contract Associate Director/Director of Biostatistics, Statistical Programmer (Some positions can be telecommuting), Sr. Clinical Data Manager, Medical Writer, Clinical Outsourcing Specialist, System Administrator/Network engineer,Regulatory Documentation Specialist, for our pharmaceutical clients in multiple locations inNorthern ...
GLOBAL CLINICAL PROTOCOL - LATE PHASE SPONSORED RESEARCH WITH ONCOLOGY REQUIREMENT #14-00927 RECRUITER: CINDI PISNOY JOB LOCATION: PLAINSBORO, NJ SEPTEMBER 2, 2014 Expected Areas of Competence: General · Manages successful execution and completion of assigned global clinical Phase IIIb/IV publication/medical informing trials within CSR&O Late Phase Sponsored Research unit, in adherence to G...
Kelly Scientific Resources Princeton, NJ
Start a new search >> Save it Upload Resume Chemist - Associate Scientist - recent grads welcome to apply! Chemist-Associate Scientist Princeton, NJ (Must be local to Princeton, NJ or Surrounding Area) This is a long term contract opportunity. Pay for this role will be $20 - $25/hr and based on experience. Kelly Services has provided outstanding employment opportunities to the most talente...
Our client, a reputable biotech company, is currently seeking a Manager, Regulatory Affairs . The Manager of Regulatory Affairs will report to the Director,Regulatory Affairs and is accountable for the preparation and management of simple andcomplex regulatory submissions. The incumbent will work independently and within agroup setting to act as liaison between Regulatory Affairs and other fun...
AAIPharma Services is a leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world. With over thirty years of drug development expertise, we offer exciting and challenging career opportunities in a dynamic and growth oriented business. Our facility is located in Edison, NJ, voted one of "America's Best Places to Live" by...
Early Clinical Development Specialist - III Must have: - BS degree (will not consider non-degreed) - Direct clinical experience (e.g. nursing) or experience conducting Phase I clinical research in the pharmaceutical industry - Phase I experience with direct tasks of regulatory document authoring (protocols, clinical study reports, IND updates), project management/oversight for Phase I studies,...
EMSL Analytical Inc is currently seeking a full time Quality Assurance Manager for it's corporate location in Cinnaminson, NJ. The Corporate Quality Assurance Manager oversees the Corporate Laboratory Quality Assurance Department. The Senior Manager of QA implements the policies and procedures of the quality management system, coordinates efforts between the analytical divisions related to the qu...
• Daily management of approximately 8 - 9 reports responsible for issuance of documentation (batch records, specifications, QIS, etc.) • Direct interaction with external clients related to documentation required for the introduction of new products. • Represents QA from a Documentation standpoint during client audits, regulatory inspections, and internal audits as directed by the Director of Qua...
Global pharmaceutical company is seeking a Director or Vice President of Quality to join their team. We are looking for a forward thinking quality professional to maintain and build upon our quality approach to providing pharmaceuticals. The Director/Vice President is responsible for the site’s quality systems ensuring the connection with manufacturing processes and business to customer needs. Yo...
Company Confidential Edison, NJ, 08837
POSITION SUMMARY: The incumbent will manage all activities of the Quality function and have overall hands-on responsibility for the development, deployment, administration and maintenance of quality systems and product control internally and at Contract Organization encompassing Biologic and Radiologic development programs. ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsibilities include, but ar...
Johnson & Johnson companies are equal opportunity employers. Associate Director - Quality Processes Liaisons-00000SSO Description Janssen Research & Development, LLC, is recruiting for an Associate Director-Quality Processes Liaisons. This is a global position and can be based at the following R&D Q&C sites: Raritan or Titusville, NJ, Spring House, PA, High Wycombe, UK, Beerse, BE, or Leiden, N...
Quality Assurance Specialist Location: Berkeley Heights NJ Duration: 6 months Requirements: -BS in the Sciences or Pharmaceutical related field is preferred with 2-4 years relevant QA experience. -Alternatively, 2 years of higher education with 4 years relevant QA experience may be acceptable. -Good computer skills and working knowledge of common business software -Good knowledge of GMP req...
Are you looking for a Clinical Research position with a large pharmaceutical or CRO company in the New Jersey, Fremont or Los Angeles, California, Research Triangle Park/Wilmington, North Carolina, or Raynam/Andover, Massachusetts areas? TechData Service has multiple positions as a Chemist II (Analytical), Clinical Research Associate III, Regulatory Affairs Specialist, Pharmacovigilance Scientist...

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