1 to 25 of 55 QMS Jobs with Remote Work Options

of the relevant regulations Provide reports to management to enable them to monitor system performance. Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. Identify and collaborate in the implementation of changes more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

management and loss prevention initiatives in order to safeguard pharmaceutical products, streamline operations, and minimise risks. KEY RESPONSIBILITIES Develop and oversee a robust quality management system in line with pharmaceutical industry regulations, including Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP). Establish quality policies, procedures, and guidelines to more »

programme Maintain network of external audit providers to support CMC, pre-clinical and clinical activities. Support the management, implementation, and maintenance of the Quality Management System to support clinical development activities. Support senior management in providing direction and leadership to staff to ensure a quality mindset is embedded in the more »

the development and validation of biomarker assays and Precision Medicine Solutions. Facilitate/participate in projects to deliver improvements to the clinical laboratory Quality Management System through collaboration with R&D Understand the business needs of PM departments, with respect to technology infrastructure, third party work and human biological sample more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

Manager. Familiarize Yourself with ISO 9001 Project Plan Identify Responsibilities, Policies, and Objectives of the Project Develop Your Project Documentation Up to Launch Quality Management System Review Performance Register for Certification Continual Improvement activities Key Responsibilities – Project Manager Quality Systems Promote Health and Safety in the workplace above everything else more »

facilities in the UK and abroad Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required experience Experience of working in a similar technical engineering role related to electrical networks, solar, battery storage more »

Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in accordance with the relevant processes (e.g. Quality Management System) To monitor project and/or support activities to ensure systems are fit for purpose, that significant risks are identified and mitigated, and that more »

all work complies with current UK legislation for work with ionizing radiation (IRR 1999, IRMER 2017) and the Trusts ISO 9001:2008-compliant Quality Management System for the provision of radiotherapy. 1.5. The post holder will be expected to prioritise and manage their own work on a day-to-day more »

and assist production team with machinery assembly, to include working overtime as and when required. · Actively support continuous improvement. · Adherence to ISO 9001 Quality Management System compliance. · Be prepared to learn a diverse set of products from differing brands and continually improve your product knowledge. Required Skills: · Experience in a more »

What You Bring In-depth understanding of continuous improvement, agile, and lean techniques to the level of Black Belt or Master Black Belt. Quality Management System ownership and development experience in line with regulatory requirements Management experience in both project and manufacturing environments. A BSc and/or MSc in more »

background in manufacturing (electronic & I or mechanical engineering). Must be familiar with and have a working knowledge of the following standards: ISO 9001 (QMS), ISO 14001 (Environmental), ISO 80079/34 (Explosive standard) Excellent communication skills Experience in leading a team If you're excited about this opportunity and more »

team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMS system Able to manage non-compliance issues and escalate when needed Have experience in the management of recalls Deal with customer, supplier, and vendor approvals more »

gather and collate that data to produce monthly and annual reporting and ad hoc reports as needed. Formalise and maintain the company’s Quality Management System for emissions and sustainability data, ensuring that there are clear written processes and standards governing the generation and collection of data. (This accountability involves more »

parent company for Eyelit, MESTEC and Optessa who are leaders in Manufacturing Execution (MES), Advanced Planning and Scheduling (APS), Manufacturing Operations (MOM), Quality Management (QMS) and Factory Automation solutions. Eyelit Technologies has delivered unmatched results for a global customer base in the manufacturing industry using cutting edge technology and advancements more »

legal & project delivery teams, as required · Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required Experience · Experience of working within a similar senior technical design role, managing multiple projects · Experience in system more »

your line manager at least every 6 months for review, making updates and amendments as necessary. • Read and Understand all assigned SOPs via the QMS system in the timeframe specified. • Ensure confidential information pertaining to the company is not divulged to 3rd parties with appropriate legal framework or permission. • Use more »

collect information for the client handover pack to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required experience network commissioning experience on renewables and utility scale projects engineers in electrical substation environments of undertaking more »

activities of outside design firms or consultants to confirm design/sizing will meet technical requirements for the contract. Ensures compliance to RJM’s QMS procedures. Prepares purchase orders for contract equipment. Reports the progress of all project activity, including significant milestones, and any conditions that would affect project cost more »

eg GC, KF, UV-Vis, FT-IR. The use of a Chromatography Data System such as Empower in a regulated laboratory. Significant experience leading QMS driven aspects of a cGMP laboratory, Laboratory error investigation, OOS investigation, Deviation investigation and CAPA. Experience scheduling and planning workloads, resource and equipment including developing more »

compliance with MRP Regulations and AS9100/AS9110 standards by conducting internal audits every 12 months. Quality Management: Establish and maintain a robust quality management system to uphold Our client Fixed Wing approvals to MRP and third-party certified requirements. Supplier Collaboration: Collaborate with Our client Supplier Quality Assurance (SQA more »

policies, processes, systems and procedures. Define the approach for the management of safety and compliance through the definition of arrangements within the Company Quality Management System Act as a customer-focused individual. Network across the Company to collaborate, leverage broader capability and the sharing of best practice Develop and support more »