The Senior Program Manager, Sterile NPI, will lead the end-to-end product development and launch processes for sterile pharmaceutical products and facilities, ensuring timelines, budgets, and quality standards are met, supporting both the VP, Innovation and embedded within the Operations & Innovation Program Management Office (PMO). This role involves managing teams remotely and on-site, requiring up to 25% travel.
Your main duties will revolve around on-site audit of our clients’ factory. Conduct food safety audits, summarize and evaluate inspection/audit findings, and communicate findings/results with client site management. Develop effective work plans for the completion of assigned inspections/audits within a determined timeframe.
The Validation Specialist is responsible for ensuring systems, equipment, processes, and software used in the manufacture, storage, and distribution of pharmaceutical products, or the management of clinical trial services, meet regulatory and internal quality standards, including key GxP-impacting computerised software. The role involves planning, executing, and documenting validation and qualification activities.
The Lead Certification Auditor performs third-party audits per SGS Certification procedures and the requirements of the applicable standards. They are responsible to make relevant decisions regarding the audit process and informs SGS CBE on issues resolution outside the audit process. The PCPC Auditor collects and analyzes sufficient information to provide a recommendation for certification.
Responsible for leading the Quality Assurance Department, you will bring deep expertise in the dietary supplement and cosmetic categories and have strong knowledge in establishing QA GMP and processes and procedures. This expertise will enable Nutrafol to continue to grow as a competitive business. As Director of QA, you will execute end-to-end QA support that will help grow and protect the business.