Search Results: 67 vacancies
...validation plans, protocols and final reports to cGMP standard.
* Review / approval of all protocols and final reports.
* Management of... ...systems requiring validation and ensuring that this activity is documented, actioned and resolved.
* This position impacts on product...
...cGMP standards.
* Generation of validation investigations and implementation of corrective actions.
* Creation, review and approval of various quality documents and test data.
* Management of validation exception events and change control processes.
* Maintenance and...
£ 43 - 56 per hour
...* Writing RCE's, placing orders, Project Management & Design review meetings.
* Working to the ASME BPE 2019 Standard and relevant... ...Acceptance Testing program.
* Coordination of all equipment documentation requirements.
* Commissioning of equipment and Engineering support...
...initial eight-month contract.
The successful individual will conduct quality-related activities such as preparing compliant documents & records; review & approval of quality records, product labels and product specification documents; and will help to support implementation...
...establish and maintain compliant product specifications
Quality review of process validation plan, protocols, and reports
Co-... ...maintaining QMS
Conduct internal audits and compilation of associated documentation
Support and assist in the preparation for customer and...
...meetings, multi-disciplinary team meetings, case conferences and review meetings as deemed appropriate.
Ensure the privacy and... ...information within the relevant staff team.
Ensure records and documentation are maintained to a high standard and storage of files is in line...
...proposals which contain technical content and designs ensuring that these are presented in a professional and concise manner.
Review and revise documents prepared by others and coordinate the preparation of those materials in a completed bid document Determine the scope and...
...Related to the product or process.
Ensure all Quality System documentation is thorough, complete, and compliant.
Audit the quality... ...Management Process including Product and Quality System document review and updates.
Generate and Providing metrics for inclusion in...
...and Regulatory standards. Responsibilities include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation . This individual contributor role requires a self-starter with expertise in QA and validation , facilitating...
€50k - €60k per annum
...on QA and compliance topics.
Manage assigned areas of the Quality Management System (QMS) for GMP compliance.
Review and approve validation documentation related to facility, equipment, and utilities.
Contribute to technology transfers and new product introduction...
...Key Responsibilities:
Prepare, execute and report on CQV documentation
Complete field verifications during static and dynamic (functional... ...necessary
Interaction with vendors for project planning
Reviewing and approving project documentation, ensuring technical...
...Stakeholder Engagement, and environmental planning application documentation)
Input into the design stage of various projects from an environmental... ...professional development, training, and periodic performance reviews to develop your career within the company.
To apply, please...
...completing computer applications
Ensure compliance with all documentation and Good Manufacturing requirements
Train new employees and... ...duties with minimal supervision
Formal goals and performance reviews conducted annually
For a confidential discussion and more information...
...impact assessments.
Maintain accurate and detailed project documentation.
Qualifications:
Bachelor's or Master's degree in Ecology... ...continued professional development, training, and periodic performance reviews to develop your career within the company.
To apply, please...
...reports for funders, stakeholders, and the board of directors, documenting achievements, challenges, and future plans.
~Become familiar with... ...~Ensure that the work of the Centre is regularly planned, reviewed, and evaluated.
~Present monthly work / progress reports to the...
...Skills Brief
Managing & coordinating the preparation, review & approval of Validation Master Plans
Generate, execute and review... ...protocols & reports
Managing & coordinating validation documentation (risk assessments, traceability matrices)
Managing & coordinating...
...establish and maintain compliant product specifications.
• Quality review of process validation plan, protocols, and reports.
• Co-... ....
• Conduct internal audits and compilation of associated documentation.
• Support and assist in the preparation for customer and surveillance...
£42.8k - £47.1k per annum
...* Support of all commissioning and validation activities during project start-up.
* Development and update of batch and cleaning documentation for NPIs
* Preparation of feasibility studies and operating budgets for future product introductions.
* Identification and process...
£ 43 - 56 per hour
...lifecycle.
* Provide technical support to all control system related issues. Tasks include, daily trouble shooting, optimisation, and documentation control.
* Leadership of control system validation activities during project start-up.
* Life cycle management of the on site...
...stages
Issuing proceedings predominantly in the Circuit and High Courts, and progressing cases to judgment
Preparing court documentation, instructing doctors, barristers, engineers etc.
The perfect candidate for this role will have experience working in Litigation...