2 jobs found in Dundee

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    • dundee, dundee
    • contract
    • £15.00 - £18.80 per hour
    • full-time
    My client, a medical device business has an exciting requirement for a Validation Engineer to join their site in Dundee on a 12 Month contract. Responsibilities include:* Prepare and manage validation activities, including document approval and protocol implementation.* Author validation documentation including, but not limited to, Installation, Operational and Performance Qualification protocols and reports, Process Validation protocols and reports, and Protocol Discrepancies and Addenda; IQ/OQ/PQ.* Ensure Standard operating procedures are adhered to in relation to current regulatory requirements/guidelines.* Create reports surrounding progression and escalating any issues effectively.* Keep current on regulatory and quality requirements for regulated testing, qualification, and validation activities.Requirements:* Degree level qualification in engineering or relevant scientific discipline.* Ideally a minimum of 1 year industry experience within medical devices. Although, this is not essential.* Experience of drafting and executing validation protocols and reports.* High attention to detail.* Excellent problem solving skills.12 Month PAYE contract. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    My client, a medical device business has an exciting requirement for a Validation Engineer to join their site in Dundee on a 12 Month contract. Responsibilities include:* Prepare and manage validation activities, including document approval and protocol implementation.* Author validation documentation including, but not limited to, Installation, Operational and Performance Qualification protocols and reports, Process Validation protocols and reports, and Protocol Discrepancies and Addenda; IQ/OQ/PQ.* Ensure Standard operating procedures are adhered to in relation to current regulatory requirements/guidelines.* Create reports surrounding progression and escalating any issues effectively.* Keep current on regulatory and quality requirements for regulated testing, qualification, and validation activities.Requirements:* Degree level qualification in engineering or relevant scientific discipline.* Ideally a minimum of 1 year industry experience within medical devices. Although, this is not essential.* Experience of drafting and executing validation protocols and reports.* High attention to detail.* Excellent problem solving skills.12 Month PAYE contract. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    • dundee, dundee
    • contract
    • full-time
    Do you have a scientific background with an understanding of process validation principles and procedures? Are you comfortable working as an individual and as part of a team? We are looking for a Manufacturing Scientist to join a pioneering organisation focused on the development and manufacturing of important and innovative in vitro diagnostic tests for use in clinical laboratories.The successful candidate will be working in a technical operations environment, the Manufacturing Scientist will be responsible for safely ensuring the on-time production of materials which conform to current best practices and quality standards, and is aligned to the expectations set by the Product Leads. This role is offered on a contract basis, initially for 5 months with the potential for extension. We have multiple roles available, across various shifts: M-F 8am-4pm or 4pm-12am. Responsibilities:Conducting all activities in accordance with the Health & Safety culture. Enthusiastically assuming responsibility for personal workload.Planning and coordinating all aspects of personal workload for specified job assignments, e.g. raw material testing, bulk reagent production, in-process testing, QC release testing, protein purifications, high-performance liquid chromatography (HPLC), etc. Performing Enterprise Resource Planning (ERP) transactions as part of works order management.Work with peers and colleagues to ensure on-time delivery of the production schedule which meets all requirements of both internal and external customers.Working to develop in-depth understanding of products, processes and procedures.Taking full accountability for personal workload, ensuring quality documentation is completed to a high standard and mistakes are rectified in a timely manner. Proactively contributing to continuous improvement initiatives and other general housekeeping duties.Taking a self-motivated approach to continuous professional development and engaging with site training initiatives/requirements. Developing excellent relations with the department team and wider Operations group. Proposing ideas for new opportunities to improve communication and productivity.Leveraging skills and experience, providing local leadership, coaching and mentoring to peers and colleagues in the Technical Operations group.Being aware of the policies as set out in the Dundee Employee Handbook and able to enact them as appropriate.Qualifications: Undergraduate/bachelor's degree in Life Sciences, Biological Sciences or Chemical Sciences.Background: A demonstrable technical understanding of the function and performance characteristics of the products and materials produced within the Technical Operations environment.A detailed knowledge of production process control procedures and best practices.An ability to navigate Electronic Document Management Systems (EDMS) and execute document control procedures. An understanding of and ability to apply Statistical Process Control (SPC) techniques, including generating trend reports.A basic appreciation for Enterprise Resource Planning (ERP) costs and how to influence them.An understanding of Corrective and preventative Action (CAPA) and Change Control principles with the ability to process records within the respective databases/systems.An ability to employ state-of-the-art Root Cause Analysis (RCA) tools, including A3/DMAIC.An understanding of and ability to contribute to Risk Assessment activities, Risk Management/Control exercises, and Failure Mode Effect Analyses (FMEA).An understanding of Process Validation principles and procedures with the ability to execute. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    Do you have a scientific background with an understanding of process validation principles and procedures? Are you comfortable working as an individual and as part of a team? We are looking for a Manufacturing Scientist to join a pioneering organisation focused on the development and manufacturing of important and innovative in vitro diagnostic tests for use in clinical laboratories.The successful candidate will be working in a technical operations environment, the Manufacturing Scientist will be responsible for safely ensuring the on-time production of materials which conform to current best practices and quality standards, and is aligned to the expectations set by the Product Leads. This role is offered on a contract basis, initially for 5 months with the potential for extension. We have multiple roles available, across various shifts: M-F 8am-4pm or 4pm-12am. Responsibilities:Conducting all activities in accordance with the Health & Safety culture. Enthusiastically assuming responsibility for personal workload.Planning and coordinating all aspects of personal workload for specified job assignments, e.g. raw material testing, bulk reagent production, in-process testing, QC release testing, protein purifications, high-performance liquid chromatography (HPLC), etc. Performing Enterprise Resource Planning (ERP) transactions as part of works order management.Work with peers and colleagues to ensure on-time delivery of the production schedule which meets all requirements of both internal and external customers.Working to develop in-depth understanding of products, processes and procedures.Taking full accountability for personal workload, ensuring quality documentation is completed to a high standard and mistakes are rectified in a timely manner. Proactively contributing to continuous improvement initiatives and other general housekeeping duties.Taking a self-motivated approach to continuous professional development and engaging with site training initiatives/requirements. Developing excellent relations with the department team and wider Operations group. Proposing ideas for new opportunities to improve communication and productivity.Leveraging skills and experience, providing local leadership, coaching and mentoring to peers and colleagues in the Technical Operations group.Being aware of the policies as set out in the Dundee Employee Handbook and able to enact them as appropriate.Qualifications: Undergraduate/bachelor's degree in Life Sciences, Biological Sciences or Chemical Sciences.Background: A demonstrable technical understanding of the function and performance characteristics of the products and materials produced within the Technical Operations environment.A detailed knowledge of production process control procedures and best practices.An ability to navigate Electronic Document Management Systems (EDMS) and execute document control procedures. An understanding of and ability to apply Statistical Process Control (SPC) techniques, including generating trend reports.A basic appreciation for Enterprise Resource Planning (ERP) costs and how to influence them.An understanding of Corrective and preventative Action (CAPA) and Change Control principles with the ability to process records within the respective databases/systems.An ability to employ state-of-the-art Root Cause Analysis (RCA) tools, including A3/DMAIC.An understanding of and ability to contribute to Risk Assessment activities, Risk Management/Control exercises, and Failure Mode Effect Analyses (FMEA).An understanding of Process Validation principles and procedures with the ability to execute. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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