10 of 10 Permanent Quality Management Jobs in Scotland

Piramal Pharma is a world-leading developer and manufacturer of high-quality biological reagents and is seeking a Quality Assurance officer to join their growing team in our QA department in Grangemouth. The Quality Assurance officer will act as the Quality Assurance representative for campaign projects, ensuring accuracy and compliance of procedures, quality management … Be the QA representative for new products and for change projects, dealing with aspects including review/approval of process instructions, change controls, deviations, investigations, validation, customer audits/quality requests, and material and product disposition. The QA officer is expected to identify, escalate and work to address any GMP/GxP issues with potential impact to product quality or quality compliance. Together we offer fantastic opportunities for committed employees to learn and develop their career with us. At Piramal , we research, develop, and supply Biopharma products and services that impact the lives of millions of people each day to make life better, and keep us safer. Your health and well-being matters to us and that More ❯

year. At Soapworks, we do more than make soap - we craft a wide range of personal care products, including hair and body cleansers and aromatic oils. We produce high-quality, sustainable soap products for leading global brands. We're looking for an experienced Quality Manager with a strong background in BRC and ISO audits to lead our Quality function, supporting our business goals and maintaining the highest standards across all aspects of quality and our management systems. The Role at a Glance: Quality Manager Glasgow - Hybrid £45,000 - £50,000 per annum + 33 days holiday, rising with service Plus Excellent Benefits Package Including Pension, Income Protection Benefit, Access to Help@Hand (EAP, GP … with a global customer base whose products Featured In: British Vogue, GLAMOUR, Elle, GQ, Beauty Bay, Stylist Magazine, HELLO! And More... Your Background/Skills: Experience of managing a quality team, experience of running BRC audits as well as the ISO audits. Quality Management, Internal & external audit management. Quality assurance for in-process and finished goods More ❯

Quality Assurance Officer (BioTech) Location: Office based, Alva, Clackmannanshire - FK12 5DQ Salary: £28,711 - £33,702 per annum, DOE plus benefits Contract: Permanent, Full time Hours: Monday - Friday 9am-5pm At AccuBio Ltd. , we don't just manufacture in vitro medical devices - we help shape the future of diagnostics and patient care. If you're passionate about quality, compliance and making a real-world impact, we want you on our team. Why this role matters: As our Quality Assurance Officer, you'll be the heartbeat of our quality operations. You won't just tick boxes - you'll elevate standards, drive innovation and embed excellence into everything we do. This is your chance to influence how … will be dynamic, purposeful and full of opportunities to grow. Key responsibilities include: Reviewing documentation for completeness, accuracy and data integrity Partnering with sourcing and operations to implement supplier quality requirements Maintaining and improving our Quality Management System into a best-in-class framework Leading CAPA, change control and non-conformance processes Measuring the success of quality More ❯

supporting a global financial services partner in sourcing an experienced Data Analyst to join a large-scale data governance and control programme. The roles will focus on improving data quality, control frameworks, and governance standards across multiple business areas while supporting functional testing and reporting activities. Assignment Details Initial Duration: 6 months (likely extension given scope) Location: Hybrid … in Business and Data Analysis , working with large datasets to identify trends, issues, and improvement opportunities Good understanding of data governance and control frameworks , including data lineage, metadata, and quality management Experience supporting functional testing (UAT/data validation) and preparing test scenarios and evidence Familiarity with data management principles across regulatory or risk environments Competent with More ❯

portfolio. Drive portfolio growth and profitability in alignment with Relm's risk appetite and business plan to ensure annual and strategic goals are achieved. Provide strong leadership, mentorship, and management to the Bermuda underwriting team, fostering a high-performance culture and supporting the professional development of junior underwriting and administrative staff. Build and maintain strong relationships with brokers, clients … as appropriate. Collaborate across teams and geographies to achieve company-wide goals, identify cross sell opportunities, and promote knowledge sharing. Support strategic underwriting planning by developing and maintaining high quality management information to evaluate portfolio performance and inform decision making. Ensure compliance with all internal and external underwriting standards, regulatory obligations, and applicable legal requirements in Bermuda and … refining policy wordings, endorsements, and underwriting guidelines. Exceptional analytical and decision making skills, with the ability to assess complex risks and design innovative insurance solutions. Excellent organisational and time management abilities, capable of managing multiple priorities in a dynamic environment. Creative problem solver with strong critical thinking skills and a proactive, diligent approach to execution. Skilled communicator-confident and More ❯

UK's largest cooked and sliced meat producers, supplying some of the country's largest supermarkets nationwide, with ambitious plans for the future. We supply an extensive range in quality cooked meats, ranging from poultry, pre-sliced and whole joints of cooked meat to convenience foods and a variety of delicatessen. It is an exciting time at Browns Manufacturing … as we continue our Scottish pork processing journey. We are currently looking for an experienced Technical Manager , to drive the technical resource of the business forward whilst supporting the management decisions of the business as a whole. As Technical Manager you will ensure the BRC standard, legislation and customer requirements are met and maintained at all times, maintain the … Quality Management System, ensuring trends are identified, reported and corrective action implemented and will also work on continuous improvement projects within the business. Reporting to the Group Technical Director, you will be responsible for ensuring the integrity of the food safety and quality of our product range and ensure that it fulfils the requirements of all customer More ❯

fermentation KPIs that can be used to identify opportunities for improvement Lead and support optimisation initiatives to increase yield, reduce cycle time, reduce costs and enhance safety and product quality Collect and analyse process data statistically and build models to support process decisions and continuous improvement. Provide subject matter expertise in aseptic design and SIP and CIP systems to … results and SOPs; contribute to IP capture and patent support. Consistently demonstrate a strong commitment to both lab and process safety. Adhere to and promote biosafety, hygienic design and quality management standards (e.g. BSL-2, GMP, FSMA, HACCP, ISO food-grade). What you can bring to the role Ideally PhD qualified in Biochemical Engineering, Biological Engineering, Fermentation More ❯

is an exciting opportunity to work across the full software development lifecycle - from defining requirements and architecture through to implementation, testing, and ongoing product enhancements - all within a collaborative, quality-driven environment. Skills & Experience Essential: Proven experience in embedded software development using C. Strong understanding of real-time systems, RTOS, and multi-threaded environments. Experience with 16/… IP), and peripheral interfaces. Experience producing technical documentation, specifications, and verification plans. Proficient with version control (Git), Jira, and unit testing frameworks (Unity, Ceedling, CMock). Knowledge of code quality standards such as MISRA. The Role Design, develop, and maintain embedded C software for medical devices to rigorous quality and regulatory standards. Define and implement technical requirements, architecture … and interface design documents in line with quality systems and design controls. Lead and participate in software reviews, ensuring best practice and high-quality output. Perform risk and impact analysis, ensuring compliance with IEC 62304 and other relevant standards. Develop and maintain low-level drivers for microcontroller peripherals (UART, SPI, I2C, etc.). Collaborate closely with hardware, systems More ❯

is an exciting opportunity to work across the full software development lifecycle - from defining requirements and architecture through to implementation, testing, and ongoing product enhancements - all within a collaborative, quality-driven environment. Skills & Experience Essential: Proven experience in embedded software development using C. Strong understanding of real-time systems, RTOS, and multi-threaded environments. Experience with 16/… IP), and peripheral interfaces. Experience producing technical documentation, specifications, and verification plans. Proficient with version control (Git), Jira, and unit testing frameworks (Unity, Ceedling, CMock). Knowledge of code quality standards such as MISRA. The Role Design, develop, and maintain embedded C software for medical devices to rigorous quality and regulatory standards. Define and implement technical requirements, architecture … and interface design documents in line with quality systems and design controls. Lead and participate in software reviews, ensuring best practice and high-quality output. Perform risk and impact analysis, ensuring compliance with IEC 62304 and other relevant standards. Develop and maintain low-level drivers for microcontroller peripherals (UART, SPI, I2C, etc.). Collaborate closely with hardware, systems More ❯

is an exciting opportunity to work across the full software development lifecycle - from defining requirements and architecture through to implementation, testing, and ongoing product enhancements - all within a collaborative, quality-driven environment. Skills & Experience Essential: Proven experience in embedded software development using C. Strong understanding of real-time systems, RTOS, and multi-threaded environments. Experience with 16/… IP), and peripheral interfaces. Experience producing technical documentation, specifications, and verification plans. Proficient with version control (Git), Jira, and unit testing frameworks (Unity, Ceedling, CMock). Knowledge of code quality standards such as MISRA. The Role Design, develop, and maintain embedded C software for medical devices to rigorous quality and regulatory standards. Define and implement technical requirements, architecture … and interface design documents in line with quality systems and design controls. Lead and participate in software reviews, ensuring best practice and high-quality output. Perform risk and impact analysis, ensuring compliance with IEC 62304 and other relevant standards. Develop and maintain low-level drivers for microcontroller peripherals (UART, SPI, I2C, etc.). Collaborate closely with hardware, systems More ❯