12 QA Specialist Jobs

Job Description QA Specialist - Project Support - 12 month Fixed Term Contract Our Client is looking to recruit a QA Specialist with at least 5 to 10 years expertise within a clinical environment. Reporting to and with the guidance of the Head of Quality Assurance … knowledge of EMA and FDA regulatory environments and requirements. Familiar with global standards related to quality e.g. ISO 9001. Experience working as a Quality Specialist or equivalent in biologics and preferably cellular and/or gene therapies. Ability to manage multiple and varied tasks and prioritize workload with more »

Quality Assurance Specialist is required by a medical device manufacturers based at Oxford Science Park, Oxford, OX4. As Quality Assurance Specialist you will be responsible for providing quality assurance, regulatory guidance across the business including manufacturing, supply chain and engineering. Other responsibilities as Quality Assurance Specialist … a fast-paced environment with minimal supervision Keywords: Quality Assurance Specialist, QA Specialist, Regulatory Specialist, Quality Assurance Manager, QA Manager, ISO9001, ISO 13485 Bond Williams Professional Recruitment are an equal opportunity employer and operate as an Employment Business and Recruitment Agency more »

Senior QA Specialist We're seeking a Senior QA Specialist to join an esteemed pharmaceutical contract services provider, known for its impressive growth and global reach. As an exclusive partner, we're excited to add a key member to their team in this pivotal … like batch review and production liaison to broader activities such as auditing, supplier management, and QMS implementation. Crucially, you'll also serve as Deputy QA Manager, with some immediate line management duties and close collaboration with the QA Manager to meet the growing demands of the site. This … to step into a senior leadership role within a fast-paced pharmaceutical environment, apply now to become part of a dedicated team. Keywords: Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change control, operations, senior, leader, supervisor more »

threats. Please find a link to our corporate video for a quick insight into Valneva Our Quality Assurance team are currently recruiting for a QA Specialist - Operations to We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical … Identify, investigate and report quality issues, escalating to management as required Participation in cross-functional projects Develop, implement and monitor Continuous Improvement activities Provide QA coaching/guidance for cross-functional groups to ensure compliance with KPI targets including functional QA if required Co-ordinate and provide training … across functional groups in Quality Procedures, cGMP requirements and QA concepts Trend and report batch review and QMS data Provide support to management during third-party audits Perform internal housekeeping, in-process visits and quality audits Perform external quality audits, supporting Livingston and other Valneva sites Implement and maintain more »

QA Specialist Moreton, GB (Hybrid) 12 Month Contract – Likely Extensions/permanency £20 per hour Function PDQ Good Manufacturing Practice (GMP) serves as the Quality Assurance Unit overseeing manufacture, testing and distribution of clinical supplies (investigational products) to assure quality and compliance with Good Manufacturing Practices (GMP more »

BioTalent have partnered up with a pioneering biotechnology company focused on developing novel cell and gene therapies, on their search for a Senior Clinical QA Specialist based at their London site. As a Senior Clinical QA Specialist you will be responsible for ensuring the … and external laboratories Provide guidance on GCP/GCLP/GLP to clinical project teams You will bring the following: Previous experience in GCP QA role, as well as working in Clinical laboratories Experience in Biologics, Steriles, CGT, or ATMP is highly desirable In depth knowledge of GCP and more »

Borehamwood, Office based | Wholesale The successful candidate will be responsible for ensuring all processes under Good Manufacturing and Good Distribution Practices are maintained and supporting and deputising in the absence of the Responsible Person for import (RPi)To support the more »

Hours : 37.5 hours per week Salary : Competitive Ref No : HRJOB9568 Business Unit : Pharma Services Location : Loughborough, Leicestershire Open To : Internal and external candidates Please note this is a re-advertisement, if you have applied for this position within the past more »

Job Title : QA Officer – Supply Chain Salary: Highly competitive with 8% annual bonus (dependent on experience) Location : Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well … established Quality team, focusing on the supply chain. We are seeking a detail-oriented and experienced QA officer with a background in pharmaceuticals (GMP) and an understanding of Good Distribution Practice (GDP). The ideal candidate will ensure compliance with regulatory standards, optimize supply chain processes, and uphold company … recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary more »

The Quality Assurance Specialist will be responsible for ensuring the standards of the Quality Management System (QMS) at CGT Catapult Stevenage are maintained in a fit for purpose state of control, and improved, for a multi-purpose, multi-client facility. This will involve maintenance and improvement of associated … develop the measures and governance structures to be employed to maintain visibility on the processes and interactions within and across them. The Quality Assurance Specialist will also be responsible for managing the Quality interactions between CGT Catapult and our Collaborators and will be the primary Quality point of … experience in interacting with the regulatory authorities (Desirable). Experience in interacting with clients and Collaborators (Desirable). Demonstrable experience working as a Quality Specialist (or equivalent) in biologics and preferably cellular and/or gene therapies. Previous exposure experience in delivering continuous improvement activities to develop GMP more »

Senior Quality Assurance Specialist The Senior Quality Assurance Specialist plays a pivotal role in fostering a culture of audit readiness within the Quality team. Responsible for overseeing Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) activities within the BioA department, this specialist is … s Audit program. Interfacing with business and functional leaders in regulated operational areas, they actively promote and support compliance. Furthermore, the Senior Quality Assurance Specialist contributes significantly to the generation of Key Quality Performance Indicators for my client's Quality Systems. Qualifications Bachelor’s degree (preferred) 3+ years more »

Job Title Quality Assurance Specialist Job Location Tewkesbury, UK Flexible, condensed or reduced working hours considered and hybrid working where possible. Job ID 8990 About this opportunity and L3Harris UK From 12 UK sites, our team of over 1,400 people deliver unique capabilities across air, land, sea more »