Job Description
We are seeking a QC Shared Services Senior Manager - QC Projects. Reporting to the Quality Control Shared Services Associate Director, this position has responsibility for the learning & development management, QC Trending Management and execution of Continuous Improvement projects.Why you should apply:You will help patients in their fight against serious diseases.You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 26.5 days annual leave, life assurance, on-site gym and gain-sharing bonus.Key Responsibilities:Leadership of QC Shared Projects team to support manufacture, testing and release of Drug Substance and Sterile Drug Product.Responsible for the Site Trending Program for Quality Control.Deliver the QC Project portfolio in line with the overall QC Strategic Objectives.Deliver continuous improvement initiatives to facilitate ongoing cost saving and performance excellence.Develop a technical training structure and associated program to facilitate ongoing and consistent learning & development across the QC organization in line with the QC Network Strategy.Ensure audit readiness, both internal and external.Ensure the QC Projects Team operates in compliance with company policies and directives, evolving Health Authority regulations and expectations.Build and foster strong relationships within the biologics quality and global quality network to drive compliance, strengthen quality systems and support company objectives.Keep abreast of current corporate and industry requirements and compliance trends as they pertain to QC.Coach, develop staff and complete performance appraisal reviews.Inspire transformative thinking and motivate employees to deliver benchmark performance.Support QC planning and scheduling activities as required.Prioritize safety in every aspect of the role.Lead by example in exemplifying safety behaviours.Qualifications & Experience:Bachelor/Masters in Science or Science related discipline with a minimum of 6 years’ experience in the Pharmaceutical Industry.Deep understanding and experience of the principles of GMP / GDP.Proven success as an accomplished people manager with the ability to motivate and develop departmental staff through effective feedback and coaching.Proven leadership skills to manage a team of professionals through changing business needs.Experience interacting with regulatory agencies.Knowledge of US and EMA GMP regulations and guidance.Demonstrated leadership, interpersonal, communication, and motivation skills.Understanding of test methods and instrumentation associated with the testing of biopharmaceutical processes including chemistry and microbiological testing.Planning and organizing skills to manage resources against timelines and project commitments; able to adjust to changing priorities and a dynamic work environment.Strong leadership and people/project management abilities with proven decision-making skills.Ability to interact with a broad range of disciplines and exert positive influence within internal matrix teams across various functions. #J-18808-Ljbffr