3 of 3 Contract Quality Management Jobs in the East of England

Morson have a great opportunity at our defence client based in Cambridge. The client is seeking an experienced Senior Quality Engineer to manage all aspects of quality within current projects. Responsibilities: Understand Quality and Project requirements. Identify quality risk and work to mitigate, manage and escalate. Oversee the process of product sign-off on completion of … the delivery process to give the customer assurance their requirements have been met. Provide quality input and advice through the product lifecycle (attend appropriate milestone/gate reviews). Identify root cause and instigate permanent corrective actions for product quality issues. Work with internal and external stakeholders to resolve quality issues that arise as quickly and efficiently … as possible to prevent compromising quality and safety standards. Liaison with Quality representatives at suppliers and subcontractors to ensure that all deliverables meet the approved specification. Review and acceptance of Supplier Quality Plans ensuring they meet contractual conditions as applicable. Support assessment of the capability and competence of potential suppliers for the customer needs Tasks: Compile and More ❯

Stevenage Hybrid work available after training 6 Month Contract - maternity cover Role Purpose As a QA Specialist in the Biopharmaceuticals Testing Laboratory (BioCTL), you will ensure full compliance with Quality Management Systems (QMS) and all relevant regulatory standards. Your work will directly support the generation, testing, and approval of laboratory data, playing a key role in the timely … document control activities, including controlled printing, reconciliation, and archiving. Assist in audit and inspection preparation and participation. Author GMP documents and maintain high documentation standards. Initiate and participate in quality events, including deviation investigations and change controls. Participate in GEMBA walks and process confirmations to drive compliance and efficiency. Scope & Accountability Direct Reports: None Indirect Reports: None Budget/… Skills & Experience Education: Bachelor of Science (or equivalent experience) in Science, Engineering, or a technical discipline. Experience: 2 years previous experience in a regulated environment, ideally GMP, in a Quality or Manufacturing support role. Laboratory experience is advantageous. Skills: Strong analytical and data interpretation skills. Proficiency in Microsoft Office. Excellent written English. Carbon60, Lorien & SRG - The Impellam Group STEM More ❯

Stevenage Hybrid work available after training 6 Month Contract - maternity cover Role Purpose As a QA Specialist in the Biopharmaceuticals Testing Laboratory (BioCTL), you will ensure full compliance with Quality Management Systems (QMS) and all relevant regulatory standards. Your work will directly support the generation, testing, and approval of laboratory data, playing a key role in the timely … document control activities, including controlled printing, reconciliation, and archiving. Assist in audit and inspection preparation and participation. Author GMP documents and maintain high documentation standards. Initiate and participate in quality events, including deviation investigations and change controls. Participate in GEMBA walks and process confirmations to drive compliance and efficiency. Scope & Accountability Direct Reports: None Indirect Reports: None Budget/… Skills & Experience Education: Bachelor of Science (or equivalent experience) in Science, Engineering, or a technical discipline. Experience: 2 years previous experience in a regulated environment, ideally GMP, in a Quality or Manufacturing support role. Laboratory experience is advantageous. Skills: Strong analytical and data interpretation skills. Proficiency in Microsoft Office. Excellent written English. Carbon60, Lorien & SRG - The Impellam Group STEM More ❯