Skip to main content

Biotech Quality Assurance Specialist Jobs

Currently, there are no Biotech Quality Assurance Specialist jobs available which match this search. You may wish to explore similar job titles on the Biotech jobs page or view related jobs below.
Here are some related jobs:
Job title: Biotech - On the floor Manufacturing - QA Specialist (JP 2410) Location: Rhode Islands,RI Contract Type: Contract Duration: 5 months + extensions Shift 2 (4 days a week Tuesday through Friday 10 hrs per day 2pm - 12am) 3Key Consulting Inc. is looking for a Specialist QA for a leading bio-pharmaceutical company. Job Details: Amgen’s Quality Assurance On the Floor Program shift 2 ...
Job title: Biotech - On the floor Manufacturing - QA Specialist (JP 2410) Location: Rhode Islands,RI Contract Type: Contract Duration: 5 months + extensions Shift 2 (4 days a week Tuesday through Friday 10 hrs per day 2pm - 12am) 3Key Consulting Inc. is looking for a Specialist QA for a leading bio-pharmaceutical company. Job Details: Amgen’s Quality Assurance On the Floor Program shift 2 ...
My client, a global innovator in speciality Biopharmaceuticals, is seeking a Quality Assurance Specialist II to join their Internal QA team as part of the Human Genetic Therapies Quality Assurance Department. As a member of the team charged with overseeing internal manufacturing, responsibilities include: support of commercial QA compliance and operations; high level deviation review and trending;...
Senior Specialist, Clinical Quality Assurance Operations Position Summary This position’s main responsibility is to support internal Study Management Teams, conduct internal and external GCP audits and to support internal Quality Assurance activities. Essential Duties & Responsibilities Conduct document reviews and audits of protocols, informed consents, clinical study reports, Investigator Br...
A growing Biopharma Co. needs a Contract – QA Specialist – for a 5 month assignment at their plant. Excellent pay rate + Travel expenses + Per diem Job Posting #: 1789 Job Title: Contract – Quality Assurance Specialist Location: Smithfield, RI Pay Rate: $30 - $50 per hr + OT 1.5X (Paid weekly via direct deposit) + Travel Expenses + per diem Contract Duration: 5 months – could be extended base...
QA Specialist IV, QA Engineering Reports to: Associate Director, QA Engineering & Validation Location: Smithfield, RI Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with devastating and rare disorders. Alexion developed and commercializes Soliris® (eculizumab), the first and only approved complement inhibitor to treat ...
TechData is looking for HEOR (Outcome Research Biostatistician),Outsourcing Manager, Biostatistician/SAS Programmer/Statistical Programmer (Some can be telecommuting), Quality Control Operations Associate, Clinical Research Scientist/Associate, also Medical Writer, Clinical Database Programmer, Sr. Study Manager, Drug Safety Associate, Clinical Data ManagerinNorthern and Central NJ.Please see belo...
Primary Role: This role is in the QA Raw Materials team of Shire Lexington Site Quality Assurance. This team includes oversight of Shire Lexington Site Warehouses, Materials Management Planning, Procurement and Warehouse operations, Raw Material batch release and Raw Material Supplier Quality on behalf of Shire. This individual will have oversight of Materials Management Warehouse Operations and...
Sr Quality Assurance Specialist - QA Raw Materials 14034BR Technical Operations Quality Regular SRPR I United States - MA - North Reading Quality Assurance Primary Role: This role is in the QA Raw Materials team of Shire Lexington Site Quality Assurance. This team includes oversight of Shire Lexington Site Warehouses, Materials Management Planning, Procurement and Warehouse operations, Ra...
Primary Role Routine management & coordination of GMP compliance systems and policies for Internal Manufacturing (MA Site). Monitors policies, processes, procedures and controls ensuring that performance and quality of products conform to established standards and agency guidelines to ensure lasting customer satisfaction. Review of production records for compliance. Assures cGMP’s and company pro...
QA Specialist II - QA Ops W-S 13608BR Technical Operations Quality Regular PROF II United States - MA - Lexington Quality Assurance Primary Role Routine management & coordination of GMP compliance systems and policies for Internal Manufacturing (MA Site). Monitors policies, processes, procedures and controls ensuring that performance and quality of products conform to established standard...
Description Responsible for executing and maintaining programs overseen by the QA Facility Support group. This includes Environmental QA (EQA), Equipment Return to Service Program (RTS) and new product launch (LCP) readiness. Additional function includes supporting a robust and sustainable Facilities Support program/strategy that will provide assurance that Oceanside facility/clean utilities and ...
Manager Quality-POS_70022464-1 Description Sanofi Genzyme focuses on developing specialty treatments for debilitating diseases that are often difficult to diagnose and treat, providing hope to patients and their families. Genzyme Corporation (a Sanofi company) and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualifie...
Novavax, Inc. (Nasdaq: NVAX) is a clinical-stage vaccine company committed to delivering novel products to prevent a broad range of infectious diseases. Our recombinant nanoparticles and adjuvant technology are the foundation for groundbreaking innovation that improves global health through safe and effective vaccines. Our product pipeline targets a variety of infectious diseases with vaccine cand...
Novavax, Inc. (Nasdaq: NVAX) is a clinical-stage vaccine company committed to delivering novel products to prevent a broad range of infectious diseases. Our recombinant nanoparticles and adjuvant technology are the foundation for groundbreaking innovation that improves global health through safe and effective vaccines. Our product pipeline targets a variety of infectious diseases with vaccine cand...
QA Specialist IV, Supplier Quality Reports to: Director, Quality Assurance Operations Location: Smithfield Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with devastating and rare disorders. Alexion developed and commercializes Soliris® (eculizumab), the first and only approved complement inhibitor to treat patients wi...
Novavax, Inc. (Nasdaq: NVAX) is a clinical-stage vaccine company committed to delivering novel products to prevent a broad range of infectious diseases. Our recombinant nanoparticles and adjuvant technology are the foundation for groundbreaking innovation that improves global health through safe and effective vaccines. Our product pipeline targets a variety of infectious diseases with vaccine cand...
Novavax, Inc. (Nasdaq: NVAX) is a clinical-stage vaccine company committed to delivering novel products to prevent a broad range of infectious diseases. Our recombinant nanoparticles and adjuvant technology are the foundation for groundbreaking innovation that improves global health through safe and effective vaccines. Our product pipeline targets a variety of infectious diseases with vaccine cand...
Job Description: QUALITY ASSURANCE SPECIALIST- Simply Biotech OVERVIEW Immediate opening for an Quality Assurance Specialist in San Diego, CA who possesses:BA or BS required in life sciences, physical sciences, engineering or other applicable technical fieldTechnical experience and knowledge in developing and coordinating quality systems compliant with FDA’s QSRsA minimum of 3-5 years in Quality ...
We are seeking a Quality Assurance Specialist III to perform a variety of activities to ensure the Safety, Quality, Identify, Purity and Strength (SQuIPS) of raw material used for cGMP manufacture of commercial and clinical products. Responsibilities include but are not limited to: Review and release of raw materials used for cGMP manufacture o Review primary data and results for raw material e...