Patient Safety Manager Western Balkans at SANDOZ INC

, , Serbia -

Full Time

Start Date

Immediate

Expiry Date

02 May, 26

Salary

0.0

Posted On

01 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Patient Safety, Regulatory Knowledge, Leadership, Communication, Audit and Inspection, Innovative Thinking, Planning, Negotiation, Organizational Skills, Interpersonal Skills, Technical Proficiency, Databases, Employee Training, Reporting, Safety Science

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape! Job Description We are looking for curious, perseverant, and purpose driven candidates for the position of Patient Safety Manager Western Balkans (Bosnia-Herzegovina, Serbia, N. Macedonia, Montenegro, territory of Kosovo, Albania), Local Responsible Person for Pharmacovigilance Serbia for a fixed term contract – replacement for maternity leave. As a Patient Safety Manager Western Balkans, you will lead and oversee pharmacovigilance activities within the local Affiliate(s), ensuring alignment with the Sandoz Pharmacovigilance (PV) System, Patient Safety (PS) organization and operating model, and associated Quality systems. This role is pivotal in guaranteeing that local safety procedures are comprehensive, effective, compliant, and seamlessly integrated within the cross-functional and global-regional-local framework. As a key member of the local Affiliate(s) organization, you play a pivotal role in promoting a comprehensive understanding of the PV system and ensuring adherence to local safety requirements. Your high visibility within the organization enables you to effectively advocate for the local Affiliate’s needs at local, regional and global levels, ensuring robust support for all safety requirements Your Key Responsibilities: Your responsibilities include, but not limited to: • Lead pharmacovigilance activities in the Sandoz affiliate, in the context of the Sandoz Pharmacovigilance System, patient safety operating model, and associated quality system, to ensure that local safety procedures are comprehensive, effective, compliant and well embedded in the cross-functional and global-regional-local environment. This includes management of local Safety information like Adverse Events, PSURs, local literature and support of business to correctly set up programs and market research. • Single point of contact: As defined by local regulations act as the National/Local Qualified Person or Local Contact Person for Pharmacovigilance in the country and act as the single point of contact with the Local Health Authority on a 24-hour basis • Establish or participate in oversight mechanisms on safety activities, specifically those outsourced to vendors on behalf of the affiliate (local activities, such as in patient-oriented programs as well as core safety activities, and core safety activities, such as case handling and periodic report generation). • Ensure the seamless flow of safety relevant information, within the affiliate, with local business partners and with regional hubs and 3rd party vendor in accordance with the Sandoz patient safety operating model. • Maintain awareness on safety profiles of Sandoz products and provide safety expertise and support for all marketed and investigational products - drugs and combination products - to other functions in the affiliate including local implementation of RMP measures. • Influence the affiliate organization as a key member of the affiliate organization with high visibility, to promote a thorough understanding of the pharmacovigilance system, adherence to safety requirements for local activities. • Participate in the maintenance of the local quality management system, including training, records management, regulatory intelligence, audit and inspection readiness, in collaboration with local, regional and global functions, business partners and vendors. • Deputize, The Manager Country Patient Safety Responsible can act as a temporary delegate for CPSR in other countries, in the context of a documented delegation plan, where the start, end and handover are described. What you’ll bring to the role: Minimum Requirements: Education: Professional qualification in Health Care Sciences (Medical Doctor, Pharmacist, Dentist) is a must. Resident of Serbia Work Experience: • Experience: Minimum 3-5 years in drug safety or pharmacovigilance (preferred) • Leadership: Demonstrated leadership and achievement in all aspects of patient safety within a local/matrix environment in the pharmaceutical industry. • Regulatory Knowledge: Extensive understanding of local and regional pharmacovigilance requirements, with the ability to address complex regulatory issues. • Process Knowledge: Proficient in pharmacovigilance processes, including compliance, databases, procedures, quality assurance, and training. Proven ability to critically evaluate and integrate data from diverse areas/domains. • Communication: Effective communication skills with various stakeholders. • Audit and Inspection: Experience in pharmacovigilance audits and inspections is strongly preferable. • Innovative Thinking: Demonstrated ability for innovative and big picture thinking. • Skills: Strong planning, negotiation, organizational, and interpersonal skills. • Technical Proficiency: Computer/IT systems literacy. Languages : • Proficiency in English: Fluent level of written and spoken English. • Proficiency in Serbian: Fluent level of written and spoken Serbian. Why Sandoz? Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! Join us! Commitment to Diversity & Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. #Sandoz Skills Desired Databases, Employee Training, Pharmacovigilance, Reporting, Safety Science, Waterfall Project Management Our Purpose here at Sandoz is pioneering access for patients. As the global leader in 'off-patent' high quality medicines, we are able to make medicine more affordable and accessible. Our broad global portfolio comprises of approximately 1,300 quality biosimilar and generic medicines, enabling us to provide more than 900 million patient treatments across 100+ countries per year, and while we are proud of this achievement, we have an ambition to do more! Powered by our talented and ambitious colleagues, who, in return for dedication and skills, experience a flexible, collaborative & inclusive culture where diversity of thought is welcomed and where personal growth is nurtured!

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Responsibilities

Lead and oversee pharmacovigilance activities within the local Affiliate(s), ensuring alignment with the Sandoz Pharmacovigilance System and associated Quality systems. Act as the single point of contact for Pharmacovigilance with local health authorities and maintain safety information flow within the affiliate.