Total 6 job vacancies by Prestige Biopharma Limited

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.

Job Description:

·      Ensure clinical trial processes and procedures are conducted in accordance with GCP, relevant regulations, guidelines, protocol, and quality management system

·      Conduct quality risk assessment and ensure appropriate mitigation of risks

·      Manage document control of quality management system

·      Review and update SOPs and associated documents

·      Prepare and conduct internal process audits, study specific audits, site audits, vendor audits and relevant audit reports

·      Perform Incident/CAPA lifecycle management including root cause analysis, impact analysis and provide suitable recommendations for improvements

·      Perform computerized system validation where required

·      Assist in the conduct of quality management review meetings

·      Keep up to date with regulatory guidelines and legislations and utilize relevant documents to interpret for guidance

·      Conduct vendor qualification

·      Review of relevant clinical trial documents

·      Management of QMS-related and study-specific training

·      Other duties as assigned by line manager/HOD

Requirements/Skills:

·      Bachelor’s degree or equivalent in basic sciences

·      Experience in pharmaceutical industry with knowledge of EU, US and other relevant international regulatory standards and GxP guidelines for the conduct of clinical trials

·      Experience in clinical/regulatory auditing desirable

·      Effective oral and written communication skill

·      Strong analytical and problem-solving skill

·      Good computer skills, inclined to adapt to technology efficiently

·      Results-oriented, multi-tasking, quick learner

About the Role 

We are seeking a highly motivated and analytical Market Research Analyst to support our commercial and business development activities in the global biosimilars market. This role sits at the intersection of market intelligence, strategy, and execution, providing critical insights to guide pipeline prioritization, partner selection, and commercialization strategies. 

The ideal candidate will have a strong life sciences background, combined with business acumen in market analysis, finance, and deal support. 

Key Responsibilities 

Market Intelligence & Analysis 

• Conduct in-depth analysis of the global biosimilars market, including market size, growth trends, regulatory landscape, and competitive dynamics 

• Track and evaluate competitor pipelines, product positioning, and commercialization strategies 

• Analyze pricing trends, reimbursement environments, and access dynamics across key markets (EU, US, APAC, etc.) 

• Develop market models and forecasts to support internal decision-making 

Business Development Support 

• Identify and evaluate potential co-development, licensing, and commercialization partners globally 

• Support business development initiatives by preparing market reports, competitor benchmarking, and opportunity assessments 

• Respond to inbound business inquiries (LinkedIn, email, etc.) in a timely and professional manner 

• Prepare briefing materials, presentations, and financial summaries for management discussions 

Partner & Stakeholder Coordination 

• Interface with regional sales and commercialization partners to gather market insights and validate assumptions 

• Coordinate cross-functionally with internal teams to gather input on capabilities, pipeline progress, and operational strengths to support company-level strategic assessments, including SWOT analysis, competitive positioning, and differentiation. 

Data Room & Documentation Management 

• Populate and maintain virtual data rooms for due diligence and partnership discussions 

• Ensure accuracy, organization, and timely updating of key documents and datasets 

Events & Meetings Coordination 

• Support planning and coordination of meetings with partners at trade shows and industry conferences 

• Assist in scheduling, preparation of materials, and follow-up actions from meetings 

Requirements 

Education & Experience 

• Bachelor’s or Master’s degree in Life Sciences (e.g., Biology, Biotechnology, Pharmacy, or related field) 

• 3–6 years of experience in market research, consulting, business development, or commercial roles within the biopharma industry 

• Prior exposure to biosimilars or biologics is highly preferred 

Skills & Competencies 

• Strong analytical and critical thinking skills, with the ability to synthesize complex data into actionable insights 

• Good understanding of pharmaceutical markets, pricing, and reimbursement mechanisms 

• Basic financial literacy (e.g., understanding of revenue models, pricing strategies, and deal structures) 

• Excellent written and verbal communication skills 

• Proficiency in PowerPoint, Excel, and data analysis tools 

• Ability to manage multiple tasks and work independently in a fast-paced environment 

Preferred Attributes 

• Experience supporting licensing or partnership deals 

• Hands-on experience with industry databases such as GlobalData, IQVIA, or similar 

• Familiarity with regulatory pathways for biosimilars (EMA, FDA, etc.) 

• Strong organizational skills and attention to detail 

• Proactive, resourceful, and collaborative mindset 

What We Offer 

• Opportunity to work in a dynamic and growing biopharma company 

• Exposure to global markets and strategic decision-making 

• Collaborative and international working environment 

당사는 한국 유가증권시장(KOSPI)에 상장된 싱가포르 국적의 바이오제약사입니다.

K-IFRS 기반 재무보고 및 공시, 기업지배구조 관련 업무를 수행할 대리~과장을모집하고 있습니다.

We are a Singapore-based biopharmaceutical company listed on the Korea Exchange (KOSPI). We are seeking a Senior Finance Executive/ Assistant Finance Manager to support key financial reporting, regulatory disclosures, and corporate governance activities in compliance with K-IFRS and KRX requirements.

Position: Senior Finance Executive / Assistant Finance Manager
Employment Type: Full-Time
Department: Finance
Location: Global Headquarters, Singapore
Reporting To: Finance Manager

Key Responsibilities

Financial Reporting & Consolidation (K-IFRS)

• Support the preparation of quarterly and annual financial statements, including audit coordination and disclosure notes
• Review consolidated financial statements to ensure accuracy and compliance with K-IFRS
• Perform reconciliation between English and Korean financial reports

Regulatory Reporting & Disclosures (KRX)

• Prepare and ensure timely submission of periodic disclosures, including annual, semi-annual, and quarterly reports
• Coordinate with internal stakeholders to gather and validate disclosure information
• Manage disclosure timelines and ensure compliance with regulatory deadlines
• Prepare and review XBRL filings in accordance with KRX requirements

Corporate Governance & Board Support

• Provide administrative and coordination support for Board of Directors (BOD), Audit Committee (AC), and Annual General Meetings (AGM)
• Assist in the preparation of board materials, resolutions, and meeting minutes

Ad Hoc & Cross-Functional Support

• Collaborate with internal departments on finance-related matters
• Support various finance projects and ad hoc assignments as required

Requirements

• Strong understanding of accounting principles and financial reporting standards
• Experience with K-IFRS consolidation and KRX disclosure reporting is highly preferred
• Proactive mindset with a strong interest in understanding the business and its operations
• Advanced proficiency in Microsoft Office (Excel, PowerPoint, Word)
• Bilingual in English and Korean, with strong written and verbal communication skills

Qualifications& Experience

• Bachelor’s degree in Finance, Accounting, Business, Economics, or related field
• Minimum 3–5 years of relevant experience in finance or accounting roles
• CPA or equivalent professional qualification is an advantage

Why Join Us

• Exposure to regional and listed company reporting requirements (KRX)
• Opportunity to work closely with senior management and governance bodies
• Dynamic and collaborative international 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.

Role Overview

We 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 Responsibilities

1. Financial Reporting & Compliance

• Oversee the full spectrum of financial accounting and reporting functions in compliance with IFRS/K-IFRS
• Manage monthly, quarterly, and annual financial closing processes
• Prepare consolidated and standalone financial statements, including notes and disclosures
• Coordinate external audits and respond to audit queries
• Ensure 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 level
• Develop rolling cash flow forecasts and monitor daily cash positions
• Conduct variance and performance analysis (monthly, quarterly, annual)
• Support business planning, including pipeline and market analysis
• Provide actionable insights to support strategic decision-making

3. Tax & Treasury Management

• Oversee all tax matters including corporate income tax, GST, and other statutory requirements
• Ensure compliance with local tax regulations and timely submissions
• Manage cash flow, working capital, and creditor payment cycles

4. Internal Controls & Process Improvement

• Establish, implement, and continuously improve internal controls and financial processes
• Identify control gaps, risks, and inefficiencies, and implement corrective actions
• Drive SAP and finance system improvements
• Strengthen governance and compliance frameworks across the organization

5. Team Leadership & Cross-functional Collaboration

• Lead and develop the finance team, including task delegation and performance management
• Collaborate with cross-functional teams to manage financial and operational risks
• Support Board of Directors and Audit Committee reporting requirements
• Partner with business units to improve financial performance and accountability

6. Corporate & Ad Hoc Responsibilities

• Support corporate governance, board reporting, and audit committee matters
• Assist other departments on financial-related matters
• Undertake special projects and ad hoc assignments as required

Requirements

Qualifications & Experience

• Chartered Accountant (CA), CPA, or equivalent professional qualification
• Minimum 10 years of relevant experience in finance and accounting
• Experience in group reporting, consolidation, and regulatory reporting preferred

Technical Skills

• Strong knowledge of IFRS / K-IFRS
• Experience with SAP or similar ERP systems
• Advanced proficiency in Microsoft Excel and MS Office tools
• Strong analytical and data interpretation skills

Core Competencies

• Strong business acumen and strategic thinking ability
• High attention to detail with strong problem-solving skills
• Ability to identify risks and implement effective controls
• Excellent communication and stakeholder management skills
• Proven leadership and team management capability

Additional Advantage

• Ability to communicate in Korean is a plus (for interaction with Korean-speaking stakeholders)

Why Join Us

• Opportunity to play a key role in a growing, dynamic organization
• Exposure to regional/group-level finance operations
• Collaborative and performance-driven work environment