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Prestige Biopharma Group Prestige Biopharma Prestige Biologics
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  • Role OverviewWe are seeking a highly capable and hands-on Finance Manager to lead the company’s financial operations, reporting, and internal controls. This role will be responsible for ensuring full compliance with IFRS/K-IFRS standards, driving financial planning and analysis, and supporting strategic decision-making across the organization.The ideal candidate combines strong technical accounting expertise with business acumen, leadership capability, and a proactive approach to process improvement.
    Key Responsibilities1. Financial Reporting & ComplianceOversee the full spectrum of financial accounting and reporting functions in compliance with IFRS/K-IFRSManage monthly, quarterly, and annual financial closing processesPrepare consolidated and standalone financial statements, including notes and disclosuresCoordinate external audits and respond to audit queriesEnsure timely and accurate regulatory filings (e.g., KRX disclosures, periodic reports)Perform reconciliation between different reporting standards (e.g., English F/S vs Korean F/S)
    2. Financial Planning & Analysis (FP&A)Lead budgeting, forecasting, and long-term financial planning at Group levelDevelop rolling cash flow forecasts and monitor daily cash positionsConduct variance and performance analysis (monthly, quarterly, annual)Support business planning, including pipeline and market analysisProvide actionable insights to support strategic decision-making
    3. Tax & Treasury ManagementOversee all tax matters including corporate income tax, GST, and other statutory requirementsEnsure compliance with local tax regulations and timely submissionsManage cash flow, working capital, and creditor payment cycles
    4. Internal Controls & Process ImprovementEstablish, implement, and continuously improve internal controls and financial processesIdentify control gaps, risks, and inefficiencies, and implement corrective actionsDrive SAP and finance system improvementsStrengthen governance and compliance frameworks across the organization
    5. Team Leadership & Cross-functional CollaborationLead and develop the finance team, including task delegation and performance managementCollaborate with cross-functional teams to manage financial and operational risksSupport Board of Directors and Audit Committee reporting requirementsPartner with business units to improve financial performance and accountability
    6. Corporate & Ad Hoc ResponsibilitiesSupport corporate governance, board reporting, and audit committee mattersAssist other departments on financial-related mattersUndertake special projects and ad hoc assignments as required

    RequirementsQualifications & ExperienceChartered Accountant (CA), CPA, or equivalent professional qualificationMinimum 10 years of relevant experience in finance and accountingExperience in group reporting, consolidation, and regulatory reporting preferred
    Technical SkillsStrong knowledge of IFRS / K-IFRSExperience with SAP or similar ERP systemsAdvanced proficiency in Microsoft Excel and MS Office toolsStrong analytical and data interpretation skills
    Core CompetenciesStrong business acumen and strategic thinking abilityHigh attention to detail with strong problem-solving skillsAbility to identify risks and implement effective controlsExcellent communication and stakeholder management skillsProven leadership and team management capability
    Additional AdvantageAbility to communicate in Korean is a plus (for interaction with Korean-speaking stakeholders)
    Why Join UsOpportunity to play a key role in a growing, dynamic organizationExposure to regional/group-level finance operationsCollaborative and performance-driven work environment

  • Job Responsibilities
    Project support: Oversee and drive project management activities by translating process development (PD) milestones (e.g., scale-up, process characterization, validation) into actionable CMC timelines. Manage comprehensive planning, timeline monitoring, and budget tracking for regulatory submissions.Project monitoring: Track and report project status to internal and external stakeholders. Leverage your hands-on process development expertise to technically evaluate CMO/CDMO manufacturing activities, proactively identifying scale-up risks, yield variations, and equipment bottlenecks.Documentation management: Manage, maintain, and critically review technical project documentation, specifically focusing on tech transfer protocols, process characterization reports, master batch records, SOPs, and meeting minutes. Facilitate the rapid collection of technical data from internal process engineers and external vendors.Stakeholder management: Act as the primary technical bridge between internal team and external partners. Coordinate collaborations, manage agreements, and oversee the scientific quality of deliverables from CMOs, CDMOs, and other vendors.Sample and logistics coordination: Handle highly sensitive project logistics, including the coordination of tech transfer materials, analytical sample shipments, and clinical drug sourcing.Regulatory support: Assist in drafting the Quality Section of dossiers for clinical trial and marketing authorization applications. Accurately translate complex PD and analytical data into regulatory documents, ensuring strict alignment with agency expectations.CMC support: Offer strategic and scientific guidance to technical teams on CMC regulatory requirements. Utilize your prior process or analytical development expertise to negotiate, troubleshoot, and resolve complex CMC-related bottlenecks.
    Job Requirements
    A Bachelor's, Master, or PhD degree in a relevant scientific discipline (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences).Proven track record in biologics Process Development, including upstream/downstream process design, optimization, scale-up, and technology transfer.In-depth knowledge and understanding of Chemistry, Manufacturing, and Controls (CMC) regulatory requirements and processes, particularly in the authoring or management of Quality sections of dossiers for clinical trial and marketing authorization applications of biologics drug.Strong collaborative skills, with the ability to work effectively with cross-functional teams, vendors, and alliance partners.Meticulous in reviewing technical documents to ensure accuracy, compliance, and completeness.Knowledge of bioprocessing, functional assays and physiochemical characterization of monoclonal antibody is a plus.

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany