Biotech Jobs in Princeton, New Jersey

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172 Princeton, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 172
Job description Head of Formulation Development These positions are responsible for independently creating and implementing formulation development strategies. Formulation leader within team based structure and provides direction for the progress of team projects. The person functions as a subject matter expert in dealing with government agencies and external contract research organizations. Co-or...
Theradex® is an international contract reserach organization providing complete professional services for the clinical research and development of pharmaceutical compoounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex® conducts studies which lead to marekting approval of significant advances; and has built a reputation on a...
Senior Drug Safety Specialist - Great Stable Company – Tremendous Growth! Our client, a multi-therapeutic pharmaceutical organization is seeking a Drug Safety Specialist/Senior Drug Safety Specialist to join their team. This is the perfect time to join this organization as the company is building their Safety team to support a robust pipeline of compounds in clinical trials. This is an immediate n...
Responsibilities: Conduct and/or assist with the conduct of audits of the Company’s projects, processes, systems and vendors as assigned and in accordance with the Annual Audit Plan with minimal supervision Facilitate or assist with facilitation of client audits and regulatory inspections Prepare audit reports Follow up to resolution of Corrective and Preventive Actions Maintain audit status up to...
Our client, one of the major pharmaceutical companies located in Princeton, NJ, is seeking a Data Analyst for a 6 month contract assignment. Primary Job Description and Responsibilities: The Pricing & Reimbursement group provides Medicaid, Chargeback, Rebate Processing, and Government Reporting services for the US Pharmaceutical business. The team is working on various projects including a major s...
Job Responsibilities: · Assist Senior Quality Management in the strategic planning, implementation and oversight of the Company's Quality program and processes · Lead the implementation of strategic initiatives within the Quality function · Assist in the development of the Annual Audit Program · Act as Subject Matter Expert in assigned Quality area(s) · Manage, supervise and mentor assigned Qualit...
Seeking Ph.D. in biochemistry, toxicology, bioanalytics or similar field and 10 + years of experience managing pharmaceutical development bioanalytics projects using Contract Research Organizations. Must have thorough knowledge of scientific operations, management, technical and administrative functions of the laboratory. Shall: * Sources, qualifies, hires and directs CRO core activities, includin...
HR Employee Services Coordinator The HR Employee Services Coordinator will be responsible for providing excellent customer service support in the area of Human Resource transactions, policies and processes to all employees through multi-channel support (i.e., phone, online, email, etc.) etc. This role is within the Human Resources Employee Services Center and provides support to employees, HR Busi...
POSITION SUMMARY: Xcenda is a premier, full-service consultancy and leading managed markets agency. For more than 2 decades, global biopharmaceutical companies as well as emerging pre-commercialization phase firms have turned to Xcenda for strategic insights, health economics and outcomes research expertise, and reimbursement support. We help manufacturers successfully commercialize innovative med...
McLane Environmental is currently seeking a staff scientist/groundwater modeler with strong data analysis and ground water modeling skills for our Princeton, New Jersey office. Applicants must have an MS degree (or BS with experience) in Geology, Hydrogeology, Environmental Science, or Environmental Engineering (or other related field) with specialization in quantitative hydrogeology and modeling....
Company Confidential Princeton, NJ, 08540
The Clinical Trial Manager is accountable for providing oversight to the site management activities outsourced to CROs for a number of phase II- IV clinical studies from planning and site feasibility through study close-out, in compliance with Sandoz processes and regulatory requirements. -Recognize potential challenge within the protocol and operational aspects of the trial and escalate to Clinic...
McLane Environmental is currently seeking a staff scientist/groundwater modeler with strong data analysis and ground water modeling skills for our Princeton, New Jersey office. Applicants must have an MS degree (or BS with experience) in Geology, Hydrogeology, Environmental Science, or Environmental Engineering (or other related field) with specialization in quantitative hydrogeology and modeling....
Job Responsibilities: Provide regulatory consultation for in-house clinical projects or stand­alone regulatory projects Compile and submit INDs/CTAs and NDAs/MAAs Maintain proficiency in current knowledge of all applicable regulatory guidelines and regulations including those regarding submissions May supervise junior regulatory staff Job Requirements: Bachelor's Degree, preferably in a life scien...
Manager, Regulatory Affairs (Labeling) Perm Opportunity Our Client a Global Pharmaceutical Company is seeking a Manager, Regulatory Affairs (Labeling) to join their team. In this critical role, you will ensure regulatory compliance in relation to Labeling and Promotional Review submissions and initiatives. Position offers competitive compensation combined with comprehensive benefits and relocation...
Our client, a pharmaceutical company, is seeking an Editor for about 4 months. Compensation $50 an hour plus benefits. Medical, Legal, Regulatory Review Process Editor Job Role: o Copyedits marketing and educational materials in accordance with AMA. o Ensures accuracy of spelling, grammar and consistency, clarity of style usage o Ensures consistency across similar material, guiding agencies and ad...
Requirements: - Associate degree or its equivalent - 1-2 years pharmaceutical industry experience in transaction processing activities - Computer proficient, strong excel and word skills. - Excellent verbal and written skills. Responsibilities: - Primarily responsible for the processing, management, follow up and filing for vendor invoices in Documentum. - Initiate payments to vendors through SAP...
Executes downstream manufacturing of clinical and commercial products. Executes pre and post processing activities such as: Clean-in-place (CIP) and Steam-in-Place of production equipment (stainless steel tanks and piping), including the operation of automated chromatography/Tangential Flow Filtration (TFF) skids. Follow Standard Operating Procedures (SOP) and Master Batch Records (MBR) as require...
Experience: Must have Oncology experience. An RN (registered nurse) is preferred. Must have an understanding of CRO/vendor management, clinical study design, CRF design, project management and familiarity with data handling. Serves as the coordinator for implementation of all clinical trial activities and management of the clinical trial in conjunction with the CRO Oversees/coordinates site visits...
Our Global Manufacturing Client is looking for a talented Senior Manager to do the following: -• Support and Manage U.S. Post-Approval regulatory activities. Track/evaluate all upcoming ANDA Annual Reports Provide monthly updates for approaching Annual Reports, to Regulatory colleagues in both Over Seas and Princeton, prioritize projects in-line with upcoming anniversary dates and assign/delegate...
Compliance Manager Pharma (Regulatory & Quality) Our Client, a Global Pharmaceutical Company is seeking a Compliance Manager to join their team. In this critical role, you will ensure regulatory compliance in relation to any field alerts and recalls; evaluate product quality complaints with regards to filing FARs and ensure compliance with Federal and State regulations. This role reports to the VP...
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