Biotech Quality Assurance Specialist Jobs

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143 Biotech Quality Assurance Specialist jobs found on Monster.

Jobs 1 to 20 of 143
Sr. Manager/Manager, Global QA Operations: Innovative, Stable Biotech Co., NJ/NYC area Summary: Our client is a truly innovative and cutting-edge Publicly-traded Biotech that has continued to explode with growth over the past several years. This opportunity offers the best of both worlds given that you will work for a true Biotech (creativity, dynamic culture, growth opportunity, flexibility, gro...
Senior Manager, Quality Systems: Attractive and Growing Biotech., NJ/NYC area Summary: We are working with a very attractive Biotech that is rapidly growing and stable. They have a newly created opening for a Senior Manager, Quality Systems. Given that this is a smaller organization, you will not be pigeon-holed and will have the opportunity to handle a diverse amount of Quality Systems responsib...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Job Details If you are a Regulatory Affairs and Compliance Associate with 3+ years of submitting drug master files, please read on...
Quality Assurance Specialistneeded for acontractopportunity with Yoh's client located inHolly Springs, NC. The Big Picture - Top Skills Should You Possess: - Quality Assurance - cGMP - Manufacturing What You'll Be Doing: - QA Shop Floor resource for primary manufacturing - Duties will include on floor batch record review concurrent to completion of manufacturing operations in real time - P...
Manager, Documentation, Global QA: Attractive and Growing Biotech., NJ/NYC area Summary: Our Biotech client has a newly created opening for a Manager, Documentation, Global QA. Given that this is a smaller organization, you will not be pigeon-holed and will have the opportunity to handle a diverse amount of QA Documentation responsibilities with the clear ability to prove yourself and take on mor...
Sr. Manager/Manager, QC, Raw Materials Innovative, Stable Biotech Co., NJ/NYC area Summary: Our client is a truly innovative and cutting-edge Publicly-traded Biotech that has continued to explode with growth over the past several years. This opportunity offers the best of both worlds given that you will work for a true Biotech (creativity, dynamic culture, growth opportunity, flexibility, ground-...
Our client a global leader in the pharmaceutical industry is looking for a Shop Floor QA Specialist - 1st shift to join the Holly Springs, NC location. DUTIES: *Hours are 6am - 3pm, Monday-Friday* Perform real time batch record/logbook review concurrent with manufacturing operations. Perform routine quality audits in Manufacturing. Support quality systems related to QA for in-process sampling...
Job Title: Shop Floor QA Specialist - 1st shift Location: Holly Springs, NC Job Description: *Hours are 6am - 3pm, Monday-Friday* Perform real time batch record/logbook review concurrent with manufacturing operations. Perform routine quality audits in Manufacturing. Support quality systems related to QA for in-process sampling and controls, and all aspects of shop floor QA. Act as quality r...
Quality Assurance Specialist II/III (Needham, MA) Overview: The QA Specialist II/III supports Quality Assurance functions focused on GMP manufacturing operations. The position will review/audit complex documents including batch records and QC data; ensure compliance to defined Quality System procedures; conduct moderate level information analysis; assure compliance to specifications and standard...
Job Title: QA Specialist Location: Holly Springs, NC Job Description: *QA Specialist I* Job Purpose Performs batch record and QC data review to support batch release in Primary QA Disposition. Supports the development and maintenance of quality procedures and systems related to Quality Assurance oversight. Provides technical support for the US FCC site in all cGMP compliance related matters, ...
Company Confidential Silver Spring, MD, 20901
QA Operations Specialist Objective: QA Operations Specialist will ensure GMP compliance with an emphasis on lot release and facility operations by providing review, organization, and oversight of records generated for GMP manufacturing use. Responsibilities: Reviewing utility and facility monitoring records Reviewing production batch lot files including batch records and supporting data Inte...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Quality Systems Specialist Nashville, TN Full-Time $70,000 - $80,000 Apply Apply Quality Systems Specialist Nashville, TN Full-Time $70,000 - $80,000 Apply Job Details Are you looking for tremendous career growth and incredible stability with an industry leader?? Based just outside of Nashville...
Kelly Services South San Francisco, CA
Documentation Specialist - Biotech Location: South San Francisco Contract: 10 months Summary: • The Documentation Specialist will support the Methods Transfer, Monitoring and External QC teams and participate in ensuring documentation is accurate, traceable and conforms to applicable SOPs and regulatory requirements. The role is designed to support data compilation, organization of information...
Description CSC has an immediate position for a Computer Validation Specialist within the DOC systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
Description CSC has an immediate position for a Computer Validation Specialist within the DOC Systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
DOCS Global Durham, NC
Summary: Expedite contract negotiation and execution by acting as a resource and liaison for the Contracts and Grants group to streamline requests to law department and avoid duplication of efforts among Contract & Grants Analysts (CGAs) and CGA management. Act as main point of contact with legal department to resolve complex legal issues while ensuring compliance with company process and strateg...
Planet Pharma Durham, NC
Planet Pharma is working with a client in Durham to hire a Site ID Specialist for contract that will last at least 6 months. This position is with for someone with at least 2 years of clinical research experience as a CRC or CTA. MUST have a Bachelor's degree. Pay is around the $20s/hour. If unable to submit here, please contact me directly at *****. RESPONSIBILITIES Take inde...
Novavax, Inc. (Nasdaq: NVAX) is a clinical-stage biopharmaceutical company creating novel vaccines to address a broad range of infectious diseases worldwide. Using innovative virus-like particle (VLP) and recombinant nanoparticle technology, as well as new and efficient manufacturing approaches, the company produces potent vaccine candidates to combat diseases, with the goal of allowing countries ...
Target HR Raritan, NJ
Company DescriptionTarget HR is associate with Target Human Resources, Inc. a Full Service Recruiting and Staffing Organization serving major companies in the New Jersey area for over Years.Job Description MAJOR BIOTECH COMPANY located in New Jersey is in immediate need of a Quality Assurance Specialist with records management experience.This is a Long Term Contract position in their Modern Resear...
Senior QA Specialist Requisition ID-00432403 Description Position Summary The primary responsibility of this position will be to ensure compliance to the Roche Pharmaceutical Quality System (PQS) quality assurance directives, global policies and standards. This role will be responsible for the development and implementation of QA review and monitoring processes to document on-going GBQC PQS c...

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