23 QA Engineering Jobs in Reading, United Kingdom

Role highlights

• As Project Quality Engineer, you are responsible for developing and implementing project quality plans that meet business, customer and con…
• Work with project, production and process teams to improve operating processes, product yields and overall quality performance.

Role highlights

• As Project Quality Engineer, you are responsible for developing and implementing project quality plans that meet business, customer and con…
• Work with project, production and process teams to improve operating processes, product yields and overall quality performance.

Role highlights

• The role: As Quality Control Engineer , you will proactively pursue continuous quality improvement activities, provide QC engineering/techn…
• As Quality Control , you will have the following: Key skills and experience: Degree or OMC/HNC equivalent Working knowledge of…

Role highlights

• Previous experience in clinical quality assurance or compliance within the pharmaceutical, biotechnology, or CRO industry.
• Conducting quality reviews of clinical trial documentation, protocols, and study reports to identify areas for improvement and ensure adher…

Role highlights

• Previous experience in clinical quality assurance or compliance within the pharmaceutical, biotechnology, or CRO industry.
• Conducting quality reviews of clinical trial documentation, protocols, and study reports to identify areas for improvement and ensure adher…

Role highlights

• Job Function: Quality Job Sub Function: Clinical Quality Job Category: Professional All Job Posting Locations: Allschwil, Basel-Country, Sw…
• Independently leads and manages the domain-specific compliance audit programs as laid down in a comprehensive audit schedule, through plann…

Role highlights

• You will be responsible for: Lead safety evaluations including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)…
• LI-Hybrid Required Skills: Preferred Skills: Clinical Operations, Compliance Management, Compliance Risk, Data Reporting, Medicines and Dev…

Role highlights

• Regulatory & Scientific Expertise Demonstrated technical knowledge and understanding of CMC drug development science(s), drug substance and…

Role highlights

• Provide high quality and consistent input to development teams and product teams to support clinical development and life cycle management…
• Work with the Systems and Operations teams to develop and continuously maintain and improve effective systems to ensure single cases…

Role highlights

• Lead the vendor lifecycle: due diligence, qualification, quality agreements, risk-based monitoring, issue management and continuous improve…
• About the role Own quality oversight of external partners supporting nonclinical and GLP activities (CROs, laboratories, test facilities).

Role highlights

• Purpose : Deliver high quality relevant Clinical Pharmacology & Pharmacometrics (CPP) documents (e.g. population PK/PD data transfer plans,…
• Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents an…

Role highlights

• You will be responsible for: Lead safety evaluations including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)…
• Provide support for Health Authority interactions regarding safety and risk management, both written and verbal.

Role highlights

• LI-Hybrid Required Skills: Medical Writing, Regulatory Writing, Submission Management Preferred Skills: Business Writing, Clinical Research…
• Coaching or mentoring more junior staff on document planning, processes, content, and provide peer review as needed; overseeing the work…

Role highlights

• Experience in interacting with cross-functional teams such as Clinical Development and Regulatory.
• Collaborate with Global Safety Officers and Safety MDs on investigational programs, including clinical trial activities and safety committe…

Role highlights

• Experience interacting with regulatory authorities and site start-up teams.
• Strong knowledge of ICH/GCP guidelines, RA, IRB/IEC regulations, and start-up processes .

Role highlights

• Prioritizes, plans and monitors allocated projects against defined timelines Develops and maintains a thorough understanding of the regulat…
• Collects and evaluates information on regulatory requirements for quality, preclinical and clinical data to meet applicable regulations.

Role highlights

• Purpose: Deliver high quality relevant Clinical Pharmacology & Pharmacometrics (CPP) documents (e.g. population PK/PD data transfer plans,…
• Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents an…

Role highlights

• Pharmaceutical industry experience in European Regulatory strategy development and regulatory procedures (including CP/DCP/MRP).
• Ensures planned drug development activities comply with Area guidelines and if they do not, provide a critical analysis of the…

Role highlights

• Support and lead process improvement and implementation across BPH. *.
• YOUR TASKS AND RESPONISIBILITIES * Leading product groups responsible for ongoing BRM and/or leading BRM activities for products of strateg…