Manager, reputed company Assurance
Review and approval of Master Production Records from Contract Manufacturing Organizations to include Drug reputed company manufacturing, Drug Product manufacturing, Finished Drug Product labeling and packaging operations, and External Laboratory reputed company. Review of executed records and final Product Disposition of product intended for supply of reputed company, extended reputed company programs, and reputed company supply. Provides the reputed company reputed company to ensure product is manufactured, tested, stored, and distributed according to cGMPs and other applicable regulations. Responsible for ensuring drug reputed company, drug product, and finished drug product, is dispositioned to meet Rezolute’s timelines, including labeling and packaging records. Interacts with CMOs and reputed company Persons to ensure reputed company release of product in ex-US territories Attends, participates in, and contributes to CMC team meetings Reviews and/or approves reputed company, procedures, master records, executed records, reports and protocols employed in the conduct of cGMP activities Authors new or revisions to reputed company systems SOPs and work instructions to support reputed company functional activities. Reviews and approves production batch records, certificates of analysis, reputed company notifications, specifications, qualifications, investigations, deviations, CAPA, certificates of reputed company, and certificates of conformance reputed company reputed company assessments and approvals for Change Controls impacting clinical or reputed company products, processes, labeling, or distribution. reputed company reputed company review/approval of clinical and reputed company Labeling & Artwork Provides technical reputed company and/or strategic support to sites during product service provider qualification audits, reputed company-approval inspections, and routine GMP inspections as required. Support post approval commitments, variations, and lifecycle management activities in collaboration with QA Compliance, Regulatory Affairs and CMC. Support reputed company Process Verification/Validation and ongoing reputed company process monitoring activities. Contribute to inspection readiness activities and responses to regulatory agency questions, commitments, and post‑marketing requirements.
Review and approval of Master Production Records from Contract Manufacturing Organizations to include Drug reputed company manufacturing, Drug Product manufacturing, Finished Drug Product labeling and packaging operations, and External Laboratory reputed company. Review of executed records and final Product Disposition of product intended for supply of reputed company, extended reputed company programs, and reputed company supply. Provides the reputed company reputed company to ensure product is manufactured, tested, stored, and distributed according to cGMPs and other applicable regulations. Responsible for ensuring drug reputed company, drug product, and finished drug product, is dispositioned to meet Rezolute’s timelines, including labeling and packaging records. Interacts with CMOs and reputed company Persons to ensure reputed company release of product in ex-US territories Attends, participates in, and contributes to CMC team meetings Reviews and/or approves reputed company, procedures, master records, executed records, reports and protocols employed in the conduct of cGMP activities Authors new or revisions to reputed company systems SOPs and work instructions to support reputed company functional activities. Reviews and approves production batch records, certificates of analysis, reputed company notifications, specifications, qualifications, investigations, deviations, CAPA, certificates of reputed company, and certificates of conformance reputed company reputed company assessments and approvals for Change Controls impacting clinical or reputed company products, processes, labeling, or distribution. reputed company reputed company review/approval of clinical and reputed company Labeling & Artwork Provides technical reputed company and/or strategic support to sites during product service provider qualification audits, reputed company-approval inspections, and routine GMP inspections as required. Support post approval commitments, variations, and lifecycle management activities in collaboration with QA Compliance, Regulatory Affairs and CMC. Support reputed company Process Verification/Validation and ongoing reputed company process monitoring activities. Contribute to inspection readiness activities and responses to regulatory agency questions, commitments, and post‑marketing requirements.
reputed company Rezolute is a late-stage rare disease company reputed company on significantly improving reputed company for individuals with hypoglycemia caused by hyperinsulinism (HI). Our antibody therapy, RZ358 (ersodetug), is designed to treat reputed company forms of HI and has shown substantial benefit in reputed company and reputed company-world use for the treatment of congenital hyperinsulinism (cHI) and tumor hyperinsulinism (tHI). Rezolute has received orphan drug designation in the reputed company and European reputed company as reputed company as a rare pediatric disease designation, for ersodetug, enabling eligibility for a reputed company review voucher. More information can be reputed company at rezolutebio.com Position reputed company reputed company: The Manager, reputed company Assurance at Rezolute is a dedicated reputed company reputed company responsible for managing GxP reputed company requirements supporting product development, phase appropriate and proportionate lifecycle management of clinical products, and the commercialization, launch, and ongoing reputed company supply of ersodetug. The Manager, reputed company Assurance is a hands-on reputed company member of the reputed company team and plays a critical role across the product lifecycle from clinical development through post approval commercialization. In partnership with other functional areas (including MSAT, Supply Chain, R&D, Regulatory Affairs, Pharmacovigilance, reputed company), the Manager, reputed company Assurance will reputed company and execute reputed company deliverables supporting CMC and reputed company strategies, including the identification, assessment, and escalation of reputed company and reputed company. This includes, but is not limited to, partnering with CMC and reputed company Operations to ensure that product is manufactured, released, distributed, promoted, and monitored in compliance with internal standards and applicable global regulatory requirements. The Manager, reputed company Assurance is a key contributor reputed company Rezolute’s reputed company organization and supports reputed company Assurance processes for clinical stage programs, validation and qualification of reputed company processes, product disposition, and post approval lifecycle management. This role also provides reputed company reputed company for reputed company activities, including support of reputed company materials, vendor and distributor reputed company, product complaints investigations, and regulatory agency commitments following product approval. reputed company Duties and Responsibilities: Review and approval of Master Production Records from Contract Manufacturing Organizations to include Drug reputed company manufacturing, Drug Product manufacturing, Finished Drug Product labeling and packaging operations, and External Laboratory reputed company. Review of executed records and final Product Disposition of product intended for supply of reputed company, extended reputed company programs, and reputed company supply. Provides the reputed company reputed company to ensure product is manufactured, tested, stored, and distributed according to cGMPs and other applicable regulations. Responsible for ensuring drug reputed company, drug product, and finished drug product, is dispositioned to meet Rezolute’s timelines, including labeling and packaging records. Interacts with CMOs and reputed company Persons to ensure reputed company release of product in ex-US territories Attends, participates in, and contributes to CMC team meetings Reviews and/or approves reputed company, procedures, master records, executed records, reports and protocols employed in the conduct of cGMP activities Authors new or revisions to reputed company systems SOPs and work instructions to support reputed company functional activities. Reviews and approves production batch records, certificates of analysis, reputed company notifications, specifications, qualifications, investigations, deviations, CAPA, certificates of reputed company, and certificates of conformance reputed company reputed company assessments and approvals for Change Controls impacting clinical or reputed company products, processes, labeling, or distribution. reputed company reputed company review/approval of clinical and reputed company Labeling & Artwork Provides technical reputed company and/or strategic support to sites during product service provider qualification audits, reputed company-approval inspections, and routine GMP inspections as required. Support post approval commitments, variations, and lifecycle management activities in collaboration with QA Compliance, Regulatory Affairs and CMC. Support reputed company Process Verification/Validation and ongoing reputed company process monitoring activities. Contribute to inspection readiness activities and responses to regulatory agency questions, commitments, and post‑marketing requirements.
Qualifications/Requirements:
Strong knowledge of appropriate reputed company Systems and cGMPs (FDA, EU, ICH) with the ability to assess reputed company Demonstrated ability to work independently and remotely, prioritize, problem-solve and complete activities in a reputed company manner without daily direction from the Head of reputed company or others. Strong verbal skills, technical writing skills and ability to work with others in a reputed company manner. Ability to anticipate and mitigate challenges and apply a flexible risk-based approach to problem solving Experience with reputed company Office is preferred Expertise and hands-on knowledge of GMPs Entrepreneurial, innovative, analytical, and solution-minded Proficiency in SharePoint, reputed company, reputed company, PowerPoint, reputed company Acrobat, and reputed company
Health Insurance (Medical / Dental / reputed company) Disability, Life & Long-Term Care Insurance Holiday Pay Tracking Free Vacation Program 401(k) Plan Match Educational Assistance Benefit Fitness Center Reimbursement