- Merck & Co. (Millsboro, DE)
- Job DescriptionThe Quality Assurance Director will provide compliance leadership and direction to our Company and contract manufacturing operation (CMO) sites that ... vaccine drug substances and finished products. As Director, you will support Quality audits and health authority inspections and ensure any resulting corrective and… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Clinical Quality Assurance Professional (QAP) position is responsible for design, delivery and execution of ... the global Clinical Quality Assurance (CQA) strategy including audit and inspection management,...and inspection management, issue management and oversight of the Quality management system. This role is responsible for Good… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionIn partnership with the Clinical Quality Operations Lead (CQOL and Head of CQO, the CQOM is accountable for the execution of operational quality ... activities within the assigned therapeutic area.- This includes operational quality management and inspection management activities.The CQOM will oversee… more
- Repligen (Waltham, MA)
- OverviewWe are seeking a Supplier Quality Engineer to join our growing Supplier Quality team. You will a key role in ensuring the quality , compliance, and ... collaborative professionals responsible for managing supplier qualification, risk mitigation, and quality performance. The team plays a key role in driving supplier… more
- Insmed Incorporated (San Diego, CA)
- …and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director of Clinical Quality Assurance (CQA) ... serves as a strategic leader managing quality and regulatory compliance related to GCPs, acts as quality lead on the gene therapy clinical development team, and… more
- Repligen (Waltham, MA)
- OverviewWe are seeking an experienced Director of Quality candidate to lead Repligen's Waltham, MA facility which has proven experience in the biotechnology ... industry. This leader will be responsible for managing the site quality assurance team which includes all day-to-day activities for product manufacture, test and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Quality Systems Lead as part of the Quality team based in Raritan, ... Lead role is an exempt level position with responsibilities for supporting the quality systems processes within a cell therapy manufacturing facility to support both… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for ... design, delivery and execution of the North America (NA) Clinical Quality Assurance (CQA) strategy including audit and inspection management and oversight of the … more
- Aequor (Irvine, CA)
- …are implemented to address the root cause of trending issues. Supports quality functions pertaining to manufacturing line support and maintenance, including SAP. ... and coordinate product/process improvements through collaboration with cross-functional teams ( Quality , Manufacturing, R&D, Supply Chain, Finance, etc.). Ensure compliance… more
- Aequor (Fort Worth, TX)
- Job Description: Job title: Associate I, Quality Control Lab - Microbiology Location: Fort Worth, TX (Onsite) Duration: 12 months Interviews: 2Job Description:Years ... for production. Conducts and analyzes in-process and final product quality analyses/inspection in compliance with standards and regulatory requirements Identifies… more
- Aequor (Thousand Oaks, CA)
- …weekend (1x/ month this is a rotation)The ideal candidate for this MCS Associate, Quality Control role will hold a bachelor's degree in Biology, Microbiology, or a ... related discipline, and bring hands-on exposure to aseptic techniques and microbiology practices, whether through academic research, internships, or industry settings. This is an onsite position requiring flexibility to occasionally work weekends or overtime,… more
- Aequor (Thousand Oaks, CA)
- …Ability to adhere to regulatory requirements, written procedures and safety guidelines Ability to evaluate documentation/data according to company and regulatory ... 1-year contract (possible extension) 100% Thousand Oaks Schedule: Monday - Friday, 8 AM - 5 PM, fully on-site The ideal candidate for this role is: A recent graduate (or early-career professional) with a Bachelor's in Biology, Chemistry, Biochemistry, or… more
- Aequor (West Greenwich, RI)
- …Science related background, lab experience Bachelor's degree OR Associate's degree and 4 years of experience OR High school diploma / GED and 6 years of experience ... 100% onsite At the Rhode Island facility Shift is Sat, Sun, Mon, Tue 6:45 AM- 5:15 PM 12 months duration with possible extension. Looking for local candidates local to the New England area, exclusively as the EW will be coming onsite to the Rhode Island (USRI)… more
- Aequor (Thousand Oaks, CA)
- …? Ability to adhere to regulatory requirements, written procedures and safety guidelines? Ability to evaluate documentation/data according to company and regulatory ... The role is 100% onsite in Thousand Oaks and follows a standard Monday-Friday 8 AM - 5 PM schedule. The ideal candidate will have a bachelor's degree in a scientific discipline and prior academic or industry laboratory experience. They should be familiar with… more
- Merck & Co. (Rahway, NJ)
- Job Description Global Quality Large Molecule Analytical Sciences (GQ- LMAS) - Analytical Transfer Team Our Manufacturing Operations teams are the people that make ... our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role OverviewThe QA Shop Floor ... Specialist is an exempt level position responsible for the floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …multiple myeloma.Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Investigation Lead is an ... Investigation Excellence Team. The QA Investigations Lead is responsible for providing quality oversight and guidance during the investigation of events that occur… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Affairs QA is responsible for providing strategic leadership and comprehensive quality oversight across all Medical Affairs programs. This role involves deputizing ... for the Sr. Director, representing the Quality organization at senior levels. The Director plays a...of excellence and compliance and working toward building a quality mindset with Medical Affairs.Support the Sr. Director's Medical… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …myeloma.Legend Biotech is seeking QA Validation Specialist I as part of the Quality team based in Raritan, NJ. Role OverviewThe QA Validation Specialist role is ... an exempt level position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …external vendors to ensure studies are conducted according to the timeline, budget and quality measures set forth by the Study teams. This leader will also ensure a ... as our Network sites) and drive the CRO to quality , cost, and shortened timelines wherever possible. The ED...support of clinical activities within the Development organization.Ensure a " Quality Mindset" is in place across the organization by… more
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