GlaxoSmithKline
Team Lead TA Quality
GlaxoSmithKline, Collegeville, Pennsylvania, United States, 19426
Site Name:
USA - Pennsylvania - Upper Providence, Durham Blackwell Street, UK - Hertfordshire - Stevenage, UK – London – New Oxford Street, USA - Massachusetts - Cambridge, USA - Massachusetts - WalthamPosted Date:
Oct 31 2024Team Lead, TA Quality
Job PurposeThe position is responsible for leading a team of Quality Business Partners that deliver independent quality expert support to stakeholders. The incumbent is a member of the QBP Therapeutic Area LT and provides input into the quality strategy of this function. The position is responsible for ensuring that quality is designed into programs and projects across therapeutic areas and for defining quality activities that ensure submission and inspection readiness.Key Responsibilities
Functional Expertise:Continually evaluate the strategic approach, drive changes in R&D QuRE processes and modify the quality strategy and plan to meet the changing needs to the organization, regulatory requirements, and industry best practices.Identify and drive continuous quality improvements as a consequence of risk assessments, audits, inspections, trends/metrics and root cause analysis.Provide input into global audit plan based on identified signals/trends/risks/gaps.Ensure rapid communication of critical quality risks and issues, including potential misconduct to business partner and QuRE management.Drive Quality by Design implementation on an asset level.Support the preparation, execution and close out of health authority inspections.Demonstrate implementation of quality strategy to health authorities.Participate/provide expertise in Due Diligence (in-licensing activities) as applicable.Leadership/People ManagementLead a team of QBP that provides experienced quality support for development (and life-cycle projects).Responsible for talent development, career development, and performance management to ensure resources are appropriately attracted, developed and deployed to deliver the quality strategy.Support the development of annual goals and objectives supporting the strategy.Contribute to the review and revision of the R&D Quality and Risk Management strategy.Lead and/or support functional initiatives as assigned.OtherMaintain the highest level of awareness, expertise in international GLP, GCP and GVP regulations, and internal policies and SOPs.May influence the external environment through interactions with regulators, trade associations or professional societies.WHY YOU?
Basic QualificationsBachelor’s degree or equivalent in scientific or quality-related field or equivalent combination of education, training and experience.Experience in pharmaceutical industry and/or quality assurance.Demonstrated ability to work in an international environment leading global quality team; with previous supervisory/management experience.Knowledge of principles and concepts of quality assurance, (quality) risk management, and quality by design.Knowledge of GLP, GCP, pharmacovigilance/drug safety and regulatory requirements, as well as analytical, organisational, and planning skills.Knowledge in the areas of oncology, immunology, respiratory, and vaccine.Other Experience / QualificationsExperience in supporting regulatory authority inspections.Knowledge of Risk-based quality management, root cause analysis and quality narrative/briefs concepts and methodology.Digital savviness, experience with AI/ML and data analytics.Ability to work effectively in an international multicultural matrix organization.Effective communication/negotiation skills and customer management skills.Experience with Veeva QMS, CTMS and Doc.
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USA - Pennsylvania - Upper Providence, Durham Blackwell Street, UK - Hertfordshire - Stevenage, UK – London – New Oxford Street, USA - Massachusetts - Cambridge, USA - Massachusetts - WalthamPosted Date:
Oct 31 2024Team Lead, TA Quality
Job PurposeThe position is responsible for leading a team of Quality Business Partners that deliver independent quality expert support to stakeholders. The incumbent is a member of the QBP Therapeutic Area LT and provides input into the quality strategy of this function. The position is responsible for ensuring that quality is designed into programs and projects across therapeutic areas and for defining quality activities that ensure submission and inspection readiness.Key Responsibilities
Functional Expertise:Continually evaluate the strategic approach, drive changes in R&D QuRE processes and modify the quality strategy and plan to meet the changing needs to the organization, regulatory requirements, and industry best practices.Identify and drive continuous quality improvements as a consequence of risk assessments, audits, inspections, trends/metrics and root cause analysis.Provide input into global audit plan based on identified signals/trends/risks/gaps.Ensure rapid communication of critical quality risks and issues, including potential misconduct to business partner and QuRE management.Drive Quality by Design implementation on an asset level.Support the preparation, execution and close out of health authority inspections.Demonstrate implementation of quality strategy to health authorities.Participate/provide expertise in Due Diligence (in-licensing activities) as applicable.Leadership/People ManagementLead a team of QBP that provides experienced quality support for development (and life-cycle projects).Responsible for talent development, career development, and performance management to ensure resources are appropriately attracted, developed and deployed to deliver the quality strategy.Support the development of annual goals and objectives supporting the strategy.Contribute to the review and revision of the R&D Quality and Risk Management strategy.Lead and/or support functional initiatives as assigned.OtherMaintain the highest level of awareness, expertise in international GLP, GCP and GVP regulations, and internal policies and SOPs.May influence the external environment through interactions with regulators, trade associations or professional societies.WHY YOU?
Basic QualificationsBachelor’s degree or equivalent in scientific or quality-related field or equivalent combination of education, training and experience.Experience in pharmaceutical industry and/or quality assurance.Demonstrated ability to work in an international environment leading global quality team; with previous supervisory/management experience.Knowledge of principles and concepts of quality assurance, (quality) risk management, and quality by design.Knowledge of GLP, GCP, pharmacovigilance/drug safety and regulatory requirements, as well as analytical, organisational, and planning skills.Knowledge in the areas of oncology, immunology, respiratory, and vaccine.Other Experience / QualificationsExperience in supporting regulatory authority inspections.Knowledge of Risk-based quality management, root cause analysis and quality narrative/briefs concepts and methodology.Digital savviness, experience with AI/ML and data analytics.Ability to work effectively in an international multicultural matrix organization.Effective communication/negotiation skills and customer management skills.Experience with Veeva QMS, CTMS and Doc.
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