Biotech Jobs in New Jersey

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312 New Jersey Biotech jobs found on Monster.

Jobs 1 to 20 of 312
Scope This position supports the regulatory manager in day to day activities to ensure the timely compilation and submission of ANDAs, annual reports, amendments, supplements and deficiency responses to the FDA. Interact and provide support to other departments including, but not limited to, PDTS, Quality Assurance, Quality Control and Manufacturing. Responsible for timely preparation and submissi...
Compression Machine Operator Needed Job requires: Pharmaceutical experience . Must be able to lift 50 lbs. Follow company policies, GMP's and Standard Operating Procedures. Pass random Drug and Alcohol screening and background check. Minimum of 1 year work experience with dependable work record. Clean drivers license Great working conditions for a pharmaceutical company. Full-time Temp to Perm Job...
The Quality Inspector checks the quality of the products that are running on the production line and inspects finished goods in accordance with standards and specifications. • Review the fill and assembly specification and the standard received from the Quality Supervisor • Enforce Current Good Manufacturing Procedures (cGMP’s) and company policies • Verify components for accuracy according to the...
Job Description Analyze laboratory samples (raw material, in-process, finished product, stability, etc. Participate in laboratory investigations when required Service laboratory equipment (calibrations, preventative maintenances, etc.) Participates in the development of other Chemists (train, mentor & guide) Comply with all applicable OSHA Safety and Health Programs Adhere to all applicable cGXP r...
· Designs experimental plan; performs pre-formulation, formulation development work and optimize formulation and process by QbD. · Involves in development of product / raw material specifications including evaluation of physicochemical properties and compatibility of raw materials. Reviews analytical data to support the product development work · Plans appropriate analytical testing and stability...
A start-up Analytics firm located in NY/NJ whose objective is to enable businesses to make better decisions using advanced analytics and scientific methods is looking for ambitious, passionate Data Scientist to join their growing team. He/She will play a key role in the firm’s data science team by serving as a technical advisor, providing state of the art analytic insights and mentoring future tea...
Senior CRA Location: Princeton NJ Duration: 6 months Requirements: -Must be Oncology nurse (RN) -Lymphoma experience preferred -Clinical oncology background is very important -Must be able to travel up to 30% of the time domestically with the possibility of international travel -Must have 3 plus years of oncology clinical trial experience in the pharmaceutical or biotechnology industry. -Must poss...
Our Pharma client in Raritan, NJ has need for a following requirement. RAVE utility study build including eCRF edit checks and custom functions RAVE web services support Support Profile Support for User Account administration RAVE and iMedidata based RAVE project creation and maintenance Provide 1st level support for RAVE application best practice and study build Review and assess RAVE release not...
Expertise: Experience in clinical data management or related discipline Experience in use and administration of RAVE electronic data capture system Experience in or exposure to additional related products e.g. iMedidata tSDV Coder Balance Designer Gateway Exposure to UAT and systems validation concepts For technical profile experience in RAVE study build and custom function development Experience...
Sr Medical Dir Immunology up to 250k base Immunology Medical Director up to 220k base all openings offer Benefits - Full Relocation Assistance Available - Possible for the ideal candidate Bonus Eligible - Yes Interview Travel Reimbursed - Yes Sr Medical Dir Immunology up to 250k base SUMMARY: The Medical Director represents a key role of all aspects related with Medical Affairs responsibilities fo...
Exciting opportunity to join a select team that is leading the way in the Pharmaceutical/Biotech industry.Competitive salary, bonus incentive program and comprehensive benefits package offered. The position will serve as a subject matter resource for identified area(s), including relevant activities in assigned Therapeutic Area program(s) or Business Objects program. Job Responsibilities: · Work w...
DESCRIPTION: Execution of local activities relevant to the management of safety data. RESPONSIBILITIES: Monitor and manage dedicated DSU mailboxes; Maintain local documentation as required by legislation (including archiving/tracking/retrieval) Lifting of boxes; Support the submission and distribution of reports and relevant tracking Support distribution and tracking of distribution of Follow-Up l...
LEO Pharma is an independent, research-based specialty pharmaceutical company committed to the discovery and development of novel drugs for patients within the area of dermatology in the U.S. For 105 years our products, which are marketed in more than 100 countries worldwide, have improved the quality of millions of people's lives around the world. We understand that people power our success. Our...
Inhalation Formulation Research Scientist Description: The Inhalation Formulation Research Scientist, Product Development fulfills a critical role in supporting the development of Inhalation products. The individual is a part of the Formulation Development team which develops dry powder and metered dose inhalers including formulation and process development, characterizes active ingredients and ex...
The Scientist IV plans, designs, and performs laboratory work towards root cause investigation of product failure and non-conformance investigation. Prepares and owns process, test method and equipment validation documentation and activities. Operates in a cross functional team consisting of representatives from Operations, Quality Assurance, and Regulatory Affairs. General Duties & Responsibiliti...
Chilly-Mazarin, IDF, 91380
Responsable des Documents Qualité Le Responsable des Documents Qualité sera responsable de la rédaction de documents qualité en conformité avec les normes requises par les autorités réglementaires et les bonnes pratiques cliniques. Ce poste est à plein temps de septembre à décembre 2014 (avec possibilité d’extension jusqu’à juillet 2015), et sera basé chez notre client (laboratoire pharmaceutique)...
Requisition ID 23864BR Title Site Specialist, Medical Reviewer Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the management and verification of medical consistency checks (MCC), management of the requirements for reporting events for adjudication (EA), and surveillance of titration of patients within clinical trials to ensure...
Executive Medical Director- (Physician); Dermatology / Auto-immune - Strategic Leadership Role –Top 5 Global Pharmaceutical Industry Leader-[RETAINED SEARCH] Position Summary: This person will work very closely with the Hiring Manager to establish development strategies for Early programs in Dermatology & Auto-Immunity and for transitioning these programs from Phase IIa to Phase IIb and into Late-...
Johnson & Johnson companies are equal opportunity employers. Principal Engineer, Polymer Processing-7177140124 Description Ethicon, Inc., now part of the Global Surgery Group of the Medical Device and Diagnostics sector of Johnson & Johnson is recruiting for a Principal Engineer - Polymer Processing, located in Somerville, NJ. The Global Surgery Innovation organization has recently integrated in 2...
Johnson & Johnson companies are equal opportunity employers. Sr. Engineer, Polymer Processing-7137140124 Description Ethicon, Inc., now part of the Global Surgery Group of the Medical Device and Diagnostics sector of Johnson & Johnson is recruiting for a Senior Engineer - Polymer Processing, located in Somerville, NJ. The Global Surgery Innovation organization has recently integrated in 2012 to su...

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