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 »
BioTalent have partnered up with a pioneering biotechnology company focused on developing novel cell and gene therapies, on their search for a Senior Clinical QASpecialist based at their London site. As a Senior Clinical QASpecialist 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 »
Job Summary QASpecialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities Provide day-to-day support and 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 »
JOB TITLE: Senior QualityAssuranceSpecialist Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality … Clinical stage biotech company who're a market leader in autoimmune diseases and we're on the hunt for a Senior Clinical QualityAssuranceSpecialist to join a well established QA function. KEY RESPONSIBILITIES: Coordinating the implementation of the company's quality management system pertaining to Good … findings. Delivering training to laboratory teams as needed. Experience Needed: Minimum 4+ years of experience in the pharmaceutical/biotechnology industry in a GCP QA role, with experience in providing quality support to clinical laboratories. Experience in providing quality support for Cell or Gene Therapy programs is highly desirable. more »
supplied to retailers, food service, B2B, and Wholesale. Due to exciting growth in the UK, the business is now looking for a QualityAssuranceSpecialist to join them at their site in Hertfordshire. On offer: Salary is £30,000 - £35,000 doe 25 days holiday Company pension Working more »
QASpecialist Moreton, GB (Hybrid) 12 Month Contract – Likely Extensions/permanency £20 per hour Function PDQ Good Manufacturing Practice (GMP) serves as the QualityAssurance Unit overseeing manufacture, testing and distribution of clinical supplies (investigational products) to assure quality and compliance with Good Manufacturing Practices (GMP 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 »
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 »
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 »
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 »
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 »