.365 days a year, our global manufacturing and supply network works to ensure our patients have the treatments they need to live longer, healthier lives.
ESO QMS Manager ensures implementation, maintenance and continuous improvement of Global ESO QMS processes, procedures and respective tools to drive standardisation and harmonization and meet applicable Novartis internal requirements and external regulations.
The ESO QMS Manager also ensures to have QA governance and oversight on document and record management activities in ESO organization and maintains knowledge with current industry trends, Health Authority expectations.
This is a temporary position for maternity leave.
Major AccountabilitiesSupports the development, implementation, and continuous improvement of NTO ESO QA processes, procedures and standards to ensure compliance with cGMP/ICH, Regulatory Authority, Novartis Quality Modules and Directives related to Supplier management.Support the Development of ESO Quality management systems.Document Management: ESO procedures governance, SOP Manager, SOP Master List, simplification initiatives, Subject Matter Expert and Single Point of Contact for standard Document Management Systems such as ESOPS D2 or CONDOR.Responsible for all necessary records regarding the Global Standard implementation as well as supporting the ESO document authors to implement the requirements described in the Global Standards.Establish strong partnership with key stakeholders.Act as a QMS representative and liaison partner in other initiatives, boards, meetings as necessary.Maintain knowledge of current industry trends and Health Authority expectations.Commitment to Diversity & InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum RequirementsThorough knowledge of cGMP.At least 5 years' experience in pharmaceutical industrial Quality and Compliance related activities or strong proved background and knowledge in GMP operations (e.G.
Manufacturing and Science).Strong analytical skills and understanding of risk management fundamentals/tools.Background in Quality and Supply Management is a must.English written, spoken and read.Good organizational, intercultural communication, and interpersonal skills.Definitive and authoritative decision-making ability, team and consensus builder, and negotiation skills.Desirable RequirementsSupplier management oversight background.Quality Risk Management experience.Experience working in a global matrix organization preferred.You'll ReceiveCompetitive salary, annual bonus, pension scheme, health insurance, flexible working arrangements, subsidized dining facilities, employee recognition scheme.
Why Consider Novartis?769 million.
That's how many lives our products touched in 2020.
#J-18808-Ljbffr