Biotech Jobs in Rahway, New Jersey

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189 Rahway, NJ Biotech jobs found on Monster.

Jobs 1 to 20 of 189
· 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...
Senior Manager Regulatory Affairs Location: Iselin, NJ Duration: 6 months Requirements: -At least a Bachelor’s degree in Life Sciences (preferably a Master’s degree) -Minimum of 10 years general Regulatory industry experience, with the preponderance of experience being in the area of Regulatory advertising and promotion review. Responsibilities: Promotional material (75%): -Collaborate wit...
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...
Our client – a growing company in central NJ, is looking for an executive level professional with extensive regulatory affairs experience in the pharmaceutical industry. Excellent salary + Bonus + relocation. Job Posting #: 1535 Job Title: Sr. Director – VP – Regulatory Affairs Overnight Travel: 5 % Location: Edison, NJ Relocation: YES – Sign on bonus to cover relocation expenses Compensatio...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Responsibilities · Propose annual financial goals and upon management approval, review quarterly performance and make necessary adjustments to ensure accomplishing the yearly goals · Develop research partnership in therapeutic proteins including both biobetter and bioinnovative entities. · Reach out to customers and connect their demands of in vitro and in vivo pharmacology to GenScript’s high ...
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...
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,...
Job Purpose: Maintains product quality by conducting microbiologic tests; communicating results. Duties: * Organizes work by confirming product specifications. * Maintains clean and safe work environment by maintaining aseptic methods and protocols; following standards and procedures; complying with legal regulations. * Prepares cultures by obtaining in-process and finished product samples. ...
Industry: Pharmaceutical Must have: - BS Life Sciences/Engineering - Experience supporting clinical trials/programs - Experience with Microsoft Project - Experience with Clinical Trial Management Systems such as Spectrum or Impact Responsibilities: · The Clinical Project Specialist will be responsible for supporting and managing the Early Stage Clinical Development functional area planning ...
Requirements: -Educated to degree level (biological science, pharmacy, or other health-related discipline preferred), equivalent nursing qualification or other equivalent experience (degree is not required) -Min 5 yrs experience within biotech/CRO or smaller company (can’t just have big pharma exp), would consider experience over degree but depends on background, (high exp working in house, they...
Peak Environmental Inc. is looking to add staff members to our environmental consulting company to address our expanding workload in the areas of environmental site assessments, investigation and remediation. This is a unique opportunity for growth at any level. Entry level candidates will find a wide variety of interesting projects to participate in; mid level candidates will find increased proje...
Please email resumes to ***** or call me at 732 429 1850. Job Title:- Clinical Research Associate II (CRA II) Location:- South Plainfield, NJ · 2 position available in NJ for Regional CRA's. with a Pharmaceuticals company · Client is looking for blood (hematology) or neurology related therapeutic study experience with 50% +/- travel. DUTIES: · Manage the study conduct of assi...
Job Description Responsibility: Responsible for the validation of stability-indicating analytical methods applicable to specific active pharmaceutical ingredients and pharmaceutical drug products Work Performed: • Perform methods development and validation using analytical techniques such as HPLC, GC, UV and FT-IR. for • API in drug substances • API, Preservatives and related degradation pro...
Responsibility: Responsible for the development and validation of In Vitro methods for Semi-solid pharmaceutical drug products. Work Performed: • Independently manage the development and validation of In Vitro methods for Semi-solid pharmaceutical drug products using Franz Cell • Technically supervise and coach junior chemists in validation and generation of IVRT data for Semi-solids • Perform...
Kerlo Research Inc. is a privately held company based in Plainsboro, New Jersey and is a specialist provider of clinical research services. In collaboration with DM Clinical Research based in Houston, TX, we are looking for a reliable, dedicated and a motivated Clinical research coordinator. We have an urgent need to fill this position as we have ongoing studies with a good number of patients enr...
Job description JOB TITLE: Associate Manager, Biologics Development LOCATION: Edison, NJ JOB DESCRIPTION AND RESPONSIBILITIES: The successful candidate will be responsible for biologics processdevelopment by working with CMO for multiple development and technology projects, providing both technical oversight and strategic guidance in a fast-paced environment. Develops high-performing cell cult...
Admera Health is an advanced molecular diagnostics company focused on personalized medicine and non-invasive cancer testing. Our goal is fulfill unmet medical needs with cost-effective tests and accurate analysis to guide patient care by utilizing next generation sequencing technologies and advanced bioinformatics to redefine disease screening, diagnosis, treatment, monitoring, and management. It ...
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...
Supervise and reports of overall product development activities to Sr.VP of R&D.Issues of meeting time line ,enhancement of personal step up activities. Analysis and resolutions for projects progression blocks of specifically of ANDA and generally other projects in lines of R&D layer out. Duties requirements encompasses solid dosage a must soft gel plus. Preformulation and as well as formulation...

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