2 of 2 Quality Management Jobs in Stevenage

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 ❯