Job Description
Company description: WuXi Biologics is a world-class biologics services provider (from discovery, through to commercialisation) with global clients in the biopharmaceutical and healthcare industries. Our mission is to accelerate and transform discovery, development and manufacturing in the fast growing field of biologics to benefit patients worldwide. The company has sites/offices in China, US, EU, Asia and Israel. The company currently employs over 5,000 employees worldwide, and are providing services to over 200+ clients globally, including 13 of the top 20 biopharmaceutical companies. Job description: QA Validation Engineer Based within the QA department, the QA Validation Engineer will be responsible for providing the company with technical and quality resources to manage the quality deliverables on projects, coordinate the necessary activities for ensuring the timely closure of internal/external quality issues and ensuring an effective quality system. Organization Description WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. Were one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. We enable our clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing. Our mission is to accelerate and transform discovery, development, and manufacturing in the rapidly growing field of biologics to benefit patients worldwide. We have sites/offices in China, the US, the EU and Asia. We currently employ over 10,000 people and provide services to more than 200 customers worldwide, including 13 of the top 20 biopharmaceutical companies. Department Description As QA Validation Engineer youll be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives.In this role youll be reporting to the QA Validation Lead. Your Responsibilities Quality review and approval of qualification/validation documentation and associated data for conformance to regulations, Standard Operating Procedures (SOPs), specifications and other applicable acceptance criteria. Work in conjunction with Engineering Departments to co-develop design verification & validation protocols for new products and for changes on existing products, review and approve protocols/studies, and perform general oversight responsibilities for the validation process (both equipment and processes). Ensure all equipment and processes are safe, effective and qualified in compliance with industry standards and regulatory expectations. Active member of the QA review board to provide overall quality direction and oversight for key functional areas (i.e. PEV, QC, Supply Chain, Engineering, CSV), ensuring that programs, policies and procedures are robust and in keeping with regulatory and client expectations. Act as a Quality point of contact and support decision making during New Product Introductions, Technology Transfer and Process Validation activities whilst ensuring that all activities meet client and regulatory expectations. Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations. Perform all activities in compliance with client safety standards and SOPs. Assist in implementation of global standards and procedures into the site Quality Systems. Provide regular reporting for KPIs, metrics, dashboards and other efforts. Participate in other projects/duties as assigned. Perform all duties in accordance with GMP requirements, SOPs and controlled documents. Flexibility to take on additional tasks and responsibilities at the discretion of the QAV Lead. Will act as a role model for the Quality function and also the wider organisation in adherence to the WuXi corporate core values and PROUD culture. Your Profile: The ideal candidate for this position will have the following: Education: A third level degree in a scientific/technical discipline (e.g. biochemistry, chemistry, engineering) would be an advantage. Knowledge/Experience: Robust experience in a Quality Engineering/Quality Assurance role for biologics, medical device or pharmaceutical manufacturing. Knowledge of Statistical Process Control and Six Sigma methodologies (Greenbelt Certification would be advantageous). Demonstrated knowledge of GxP regulations (e.g. EU-GMP, FDA, ISO). Understanding of principles of Validation and New Product Introduction and be familiar with Computerised System Validation, Method Validation, Shipping Validation, Cleaning Validation and Process Validation. Experience in change control, non-conformance, corrective and preventative actions, and validation practices. Personal skills: Ability to operate across functional boundaries, both internal and external. Independent, self-motivated, organized, able to multi-task in project environments and skilled in communication and collaboration. Prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making. Critical thinking skills. Mobility in regard to domestic & international travel is a prerequisite. As we extend our global reach, we need colleagues interested in change, in challenge, and in building a new future together. Reach beyond yourself and discover your true potential! If you have the ability to thrive in a dynamic and fast-paced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our mission - Any drug can be made, and any disease can be treated - dont miss out on this opportunity to join us and reach beyond yourself and discover your true potential. Apply now! Would you like to know more before you apply? Please visit us at or contact us via WuXi Biologics is an equal opportunities employer. Skills: Problem Solving Analytical skills Attention to Detail Benefits: Bonus Parking Pension Staff discount VHI