Biotech Jobs in Trenton, New Jersey

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140 Trenton, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 140
FORMULATIONS ASSOCIATE Position Summary: This role will be to design and execute formulation development related studies for ANDA submission. Accountable for formulation and process development from project inception through transfer to commercial process validation, the Formulation Associate will work under and in coordination with the Product Development Specialist Essential Job Functions: •...
QUALITY CONTROL ANALYTICAL CHEMIST Bio-Pharm Inc. is a leading manufacturer and supplier of generic pharmaceutical formulations. Reporting directly to the Quality Control Manager, the Analytica Chemist will coordinate with other Quality Control chemists, R&D researchers and formulation specialists and other manufacturing departments to ensure high quality standards are always met. Major Tasks, K...
Job Title: Documentation Coordinator Position Description Knowledge of biotech bulk and finished product manufacturing, analytical testing is preferred. Knowledge of US and EU cGMP regulations and guidance. Knowledge of SAP, LIMS, Trackwise, Smartlab are a plus Position Responsibilities Releases raw materials, in-process materials, and finished product Investigates and resolves deviations a...
Job Title: Clinical Program Manager Position Description Clinical Program Management Leader (CPML) for the Neuroscience PMO Experience in multiple areas is preferred. Experience with Phase 1-3 clinical programs and a non-traditional drug development model is preferred. Experience with working with external partners is preferred. Demonstrated track record of cross-functional/matrix team manag...
Johnson & Johnson companies are equal opportunity employers. Senior Manager - Incentive Compensation Design-1754141208 Description Janssen Pharmaceuticals, Inc. is recruiting for a Senior Manager, Incentive Compensation Design, to be located in Titusville, NJ. Janssen Pharmaceuticals, Inc., a pharmaceutical company of Johnson & Johnson, provides medicines for an array of health concerns in sev...
POSITION SUMMARY: Under general direction of the Director, Clinical, the Assistant Director will be a primary contributor to the development and management of scientific and medical writing projects, including US and global product dossiers, publications and research protocols. The candidate will also serve as a clinical resource across business functions. PRIMARY DUTIES AND RESPONSIBILITIES: D...
Associate Director, Quality Assurance and Document Review System One has engaged with a Top Client in a search for a Associate Director of Quality Assurance (Document Control) In this critical role you will be required to check and ensure the quality and accurateness of all pre-submission documentation for FDA approval. This critical task must be accompanied by and audit trail in paper or electr...
Hi, We currently have An excellent opening for an Engineer - Degree Optional I in PRINCETON, New Jersey but we also have other opportunities so don't let this description stop you from SENDING ME YOUR RESUME and calling me so we can talk about what would be the perfect career move for you. I have several openings and new opportunities come in all the time so please don't hesitate to ask me what i...
At Dr. Reddy’s, a global pharmaceutical company, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a differenc...
Serve as a lead on FDA Regulations governing Labeling of Rx and OTC pharmaceutical products, as well as, Cosmetic products. Provide leadership and guidance to employees on commonly practiced procedures while being responsible for coordinating, reviewing and finalizing submission ready product labels in applicable formats to support the submission and approval of products. In addition, assist with ...
Sr Associate Regulatory Affairs (CMC) Our client a global pharmaceutical organization is seeking a Regulatory Affairs Senior Associate to join their team. This is an exciting time to join this organization as they recently brought several new products to market. Great full-time permanent opportunity! Position offers tremendous growth, competitive compensation, comprehensive benefits and a reward...
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 reloca...
POSITION SUMMARY: This isa full-time or contract position responsible for overseeing all clinical trial activities from start to finish for US and International studies. This includes trials necessitated by R&D, Regulatory and Marketing. ESSENTIAL DUTIES AND RESPONSIBILITIES: Manage clinical study monitors and interact with investigational sites. Oversee and Manage Contract Research Organizati...
inVentiv Health – Transforming Promising Ideas into Commercial Reality Job Title: Sr. Clinical QA Auditor Job Description: · 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 inspectio...
KVK-TECH is a leading American developer, manufacturer and marketer of specialty pharmaceuticals. KVK-TECH’s 110,000 square ft. state of the art facilities are located in Newtown, Pennsylvania. These facilities are organized to accommodate the company’s entire business operation including product development, manufacturing, packaging/labeling, quality control, and sales and marketing. The company...
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...
Intellisphere, LLC a Princeton, NJ-area medical publisher is looking for an experienced professional with clinical and communications experience to provide support and oversight for editorial projects covering a wide variety of publication properties. Projects span a variety of therapeutic areas including cardiology, endocrinology, oncology, psychiatry and others. Additionally, this position assis...
Company Confidential East Windsor, NJ
Aprecia Pharmaceuticals is hiring a Materials Manager. The ideal candidate will be responsible for the planning, controlling, purchasing, and the storing of raw materials and finished goods, all while maintaining cGMP Compliance. Description of Duties: Position will be effectively planning, managing and purchasing all raw materials, components, and processed goods as well as controlling all phar...
Have a passion for science, technology, engineering or math? Ever consider a career in teaching? We can help. The Woodrow Wilson Teaching Fellowship recruits the nation’s best and brightest recent college graduates and career changers in STEM fields (science, technology, engineering, or math) with a $30,000 stipend to complete an intensive one-year master's degree program in teaching at one of o...
RESEARCH SCIENTIST FOR SMALL AND MILLAMOLECULE TESTING REQUIREMENT #14-01345 RECRUITER: JESSICA CLARK JOB LOCATION: LAWRENCEVILLE, NJ DECEMBER 17, 2014 Project Description: In addition to chiral purification support for lead optimization and in-process scale up of small molecules, demand for SPS activities at the client site is at an all-time high. This is due to physicochemical characterizat...

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