Job Description QASpecialist - Project Support - 12 month Fixed Term Contract Our Client is looking to recruit a QASpecialist with at least 5 to 10 years expertise within a clinical environment. Reporting to and with the guidance of the Head of QualityAssurance … knowledge of EMA and FDA regulatory environments and requirements. Familiar with global standards related to quality e.g. ISO 9001. Experience working as a QualitySpecialist or equivalent in biologics and preferably cellular and/or gene therapies. Ability to manage multiple and varied tasks and prioritize workload with more »
QualityAssuranceSpecialist is required by a medical device manufacturers based at Oxford Science Park, Oxford, OX4. As QualityAssuranceSpecialist you will be responsible for providing qualityassurance, regulatory guidance across the business including manufacturing, supply chain and engineering. Other responsibilities as QualityAssuranceSpecialist … a fast-paced environment with minimal supervision Keywords: QualityAssuranceSpecialist, QASpecialist, Regulatory Specialist, QualityAssurance 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 QASpecialist We're seeking a Senior QASpecialist 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 QualityAssurance team are currently recruiting for a QASpecialist - 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 »
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 »
Loughborough, Leicestershire, East Midlands, United Kingdom Hybrid / WFH Options
Almac Group (Uk) Ltd
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 »
Maidenhead, England, United Kingdom Hybrid / WFH Options
SRG
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 QualityAssuranceSpecialist 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 QualityAssuranceSpecialist 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 QualitySpecialist (or equivalent) in biologics and preferably cellular and/or gene therapies. Previous exposure experience in delivering continuous improvement activities to develop GMP more »
Senior QualityAssuranceSpecialist The Senior QualityAssuranceSpecialist 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 QualityAssuranceSpecialist contributes significantly to the generation of Key Quality Performance Indicators for my client's Quality Systems. Qualifications Bachelor’s degree (preferred) 3+ years more »
Tewkesbury, Gloucestershire, South West, United Kingdom Hybrid / WFH Options
L3Harris Technologies UK Ltd
Job Title QualityAssuranceSpecialist 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 »