Stevenage, Hertfordshire, South East, United Kingdom
Russell Taylor Group Ltd
for qualitymanagement, quality assurance, and quality auditing tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPA and change control for which you are the owner are progressed in a compliant and timely manner and all other items are … a timely manner in line with company procedures. Participate and/or host internal and external audits inclusive of customer and regulatory audits. Competent to author and approve routine QMS activities. Performing Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the … site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required. Ensure customer or supplier complaints are satisfactorily investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review More ❯
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Role Overview: This role is joining our dynamic team in Manufacturing Technology (Process & Manufacturing Engineering) where you will be supporting the More ❯
matters. Assist with third-party and customer audits, including the implementation of corrective actions. Manage the internal audit programme, perform internal audits, and oversee corrective actions. Maintain the QualityManagementSystem, including inspection and test data and quality records. Support resolution of customer complaints in collaboration with the Quality team. Create and maintain Quality Plans to ensure compliance with contract … technical drawings and specifications. Familiarity with Geometric Dimensioning & Tolerancing is a plus. Good understanding of manufacturing processes and quality control systems. Required Experience: Working knowledge of ISO 9001 QualityManagementSystem standards and practices. Familiarity with mechanical inspection equipment; experience with CMM or FARO arm is a plus. Experience managing calibration systems and document control. Competence in developing and applying More ❯
Job Title: Senior QA Specialist Salary: £38,000 - £45,000 Location: Greater Manchester SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all More ❯
a key role within the Quality team, reporting to the Quality Manager and responsible for leading a team of QA professionals while maintaining and developing the site's QualityManagementSystem in line with customer, legal, and audit requirements. Key Responsibilities: Oversee and improve the QualityManagementSystem, ensuring compliance with customer and legal standards Lead investigations into complaints and … improvement initiatives What We're Looking For: Degree in a food-related discipline or minimum 5 years' QA experience within FMCG Strong knowledge of BRC standards, internal auditing, and QMS implementation Proficient in Microsoft Office, with strong attention to detail and reporting skills Experience in team leadership or coaching is desirable Previous involvement in third-party or customer audits is More ❯
third party surveillance and customer audits, including corrective actions that arise. Manage the internal audit programme, perform internal audits and manage corrective actions that arise. Maintenance of the QualityManagementSystem, including maintaining inspection and test data across local Qualitysystem records. Assist the Quality Director and Quality Manager in resolving customer complaints. Produce Quality Plans to ensure compliance with … others. Ability to read technical drawings and specifications. Geometrical Dimensioning & Tolerancing knowledge is an advantage. Thorough knowledge of fundamental manufacturing processes and control systems. Experience required in: ISO9001 QualityManagementSystem requirements and maintaining a QMS. Mechanical measuring and inspection equipment. CMM or FARO arm experience would be an advantage. Calibration systems and control. Documentation systems and control. Raising and More ❯
This approach is fully embraced throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our qualitymanagementsystem ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its obligations to act responsibly, ethically More ❯
Inverness, Inverness-Shire, Scotland, United Kingdom
DPS Group
This approach is fully embraced throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our qualitymanagementsystem ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its obligations to act responsibly, ethically More ❯
experience with deep understanding of GxP regulations, FDA 21 CFR Part 11 compliance, and validation methodologies •? Design and develop complex integration flows connecting S/4HANA with LIMS, MES, QMS, and regulatory reporting systems using REST, SOAP, OData, IDoc, RFC protocols •? Lead and mentor team of 6-10 integration developers while collaborating with functional consultants and business stakeholders •? Ensure regulatory More ❯
for purpose managementsystem is in place covering, quality, safety, security, health and environmental issues. Facilitate the implementation of the QSSHE management system. Support the maintenance of the QualityManagementSystem utilised within the office. Provide leadership to the SNS organisation on quality issues. Support SNS QSSHE Team in the delivery of day-to-day activities such as Total Risk More ❯
qualitysystem to ISO 13485 standards and associated product certification. As a Quality Systems Engineer, you will: Support the maintenance and continuous improvement of our ISO 13485 compliant QualityManagementSystem with activities including document control, training management and change management. Draft and update procedures, work instructions, and quality documentation. Collaborate closely with Engineering (Software and Hardware) and Customer Support More ❯
for a Quality Assurance Manager to join an industry leading baker of a variety of delicious treats and cakes. You will be accountable for the implementation of the QualityManagementsystem site policies and procedures. Driving for compliance to site standards and continuous improvement of food safety/product quality/legality and food safety culture. Key accountabilities as QualityMore ❯
that arise; communicate and escalate as required Deliver the quality message around site through team training, presentations and tool box talks Support the monitoring and compliance of the QualityManagementSystem as it applies to site Operations Plan, conduct and review inspections for all areas as per the inspection plan. Communicate findings and work with areas leads to implement corrective More ❯
that arise; communicate and escalate as required Deliver the quality message around site through team training, presentations and tool box talks Support the monitoring and compliance of the QualityManagementSystem as it applies to site Operations Plan, conduct and review inspections for all areas as per the inspection plan. Communicate findings and work with areas leads to implement corrective More ❯
This approach is fully embraced throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our qualitymanagementsystem ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its obligations to act responsibly, ethically More ❯
communication with internal employees, managers, and customers, as needed. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's QualityManagementSystem policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to work on a mobile device More ❯
root cause analysis investigations for internal non-conformances. Support continuous improvement teams for quality improvement and waste reduction. Support the QC manager in ensuring standards defined within the qualitymanagementsystem are maintained and reflect the correct standards to match customer expectation. To highlight inconsistencies and errors within QC documentation and processes Ensure these are recorded in an appropriate manner More ❯
We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the QualityManagementSystem (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯
Leighton Buzzard, Bedfordshire, South East, United Kingdom
1TECH STAFFING LIMITED
We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the QualityManagementSystem (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯
Manchester, North West, United Kingdom Hybrid / WFH Options
Genedrive
Regulatory Affairs Specialist to join their QA/RA team on a 12-month maternity cover contract. Key Responsibilities: Lead and support continuous improvements within the QualityManagementSystem (QMS) Collaborate with all departments and external stakeholders to maintain regulatory compliance Provide QA/RA expertise throughout product development and change control processes Guide risk management and post-market surveillance … Review SOPs, software development documents, and regulatory submissions Deliver training to ensure quality and regulatory understanding across the business Perform internal and supplier audits and support external inspections Validate QMS-related software and manage eQMS platforms Assist in compiling and maintaining technical and regulatory documentation Benefits At Genedrive, youll be part of a passionate and expert team, making a tangible More ❯
to identify areas for reliability and quality improvement; initiating and facilitating actions to implement improvements effectively using problem-solving techniques (8D, 5Why, etc.). Responsibility for the maintenance of QMS, ensuring compliance with all regulatory requirements and standards adopted by the company. Formulate, develop, and promote policies, processes, procedures, objectives, and measures for the continued operation of QMS (e.g., Quality … instructions for company processes and procedures. Organise and conduct internal and external audits to ensure adherence to regulations and standards. Collate and deliver performance data as part of the QMS review to senior management. Identify training needs and implement company-wide compliance training. Train and coach staff regarding quality and environment functions. Establish quality contracts with customers and suppliers. Act More ❯
for improvement and develop actionable solutions. Willing to gain further qualifications in operational business management. Good knowledge of budgeting, forecasting, and financial reporting as it relates to operational management. QMS or process-driven system creation/management of document systems and control systems. We are an equal opportunities employer, and we welcome applicants no matter what their ethnicity, gender, sexuality More ❯
progress, co-ordination and feedback Responsible for the production, review and monitoring of construction methodology documentation including RAMS and ITP's to ensuring compliance with the company's qualitymanagementsystem and the employers requirements. Responsible for production of as-built documentation from site. Responsible for materials forecast, procurement and reconciliation. Help collate and site data for inclusion in Daily More ❯
communication skills to team, peers, and all levels of management Desired Characteristics NPI process knowledge/experience Test Systems Sustainment process knowledge/experience Familiar with highly regulated QualityManagementSystem(s) Good people skills and a firm interest in developing engineers. An appetite to drive Continuous Improvement initiatives and invest in process development/refinement. GE supports and encourages More ❯
Review and sign off all direct reports’ timecards and expenses. Authorise Holiday requests of direct reports. Maintain register and carry out technical audits on projects as required. Ensure QualityManagementSystem ISO 9001and 14001. Preferred Skills and Experience Excellent presentation and communication skills. Extensive experience, especially in designing and managing projects, minimum 10 years’ experience within a design consultancy working More ❯