Develop compelling and effective marketing copy for various communication materials, including brochures, presentations, website content, and other marketing collateral.
Write, edit, and optimize SEO-driven articles and website content to improve search visibility and support digital marketing objectives.
Collaborate with cross-functional teams, including research & development, product, and design, to ensure consistent brand messaging across all communication channels.
Ensure all written materials align with the company's brand voice, tone, and communication guidelines.
Stay up-to-date with content marketing, SEO, and digital communication best practices to continuously enhance content effectiveness.
Review, proofread, and edit content to maintain accuracy, clarity, and quality before publication.
Have a strong background in Marketing Communications or a related field, with a minimum of 2 years of professional experience. Experience in the life sciences or related industries is highly preferred.
Proven experience in developing and executing integrated marketing communication plans that drive audience engagement and measurable business impact.
Demonstrated ability to create high-quality marketing and educational content, including brochures, articles, website content, presentations, and multimedia assets.
Creative thinker, continuously exploring innovative marketing strategies and tools.
Ability to translate complex scientific, technical, or healthcare-related information into clear, engaging, and audience-friendly content.
Strong understanding of content marketing, digital marketing, SEO principles, and multi-channel communication strategies.
Strong attention to detail with the ability to maintain content accuracy, quality, and brand consistency.
Able to manage multiple projects simultaneously and work effectively in a fast-paced environment while meeting deadlines.
Advise the leadership team on legal and compliance matters critical to the growth of the business, with a strong understanding of the company’s business model and cross-departmental needs.
Anticipate and plan for all legal risks and develop strategies to mitigate those risks, aligned with business objectives.
Lead, manage, and delegate tasks effectively within the legal and regulatory team to ensure reliable and timely execution of day-to-day activities.
Act as a business partner to internal stakeholders by understanding requests from various departments and translating them into actionable legal strategies and support.
Draft, review, recommend revisions as needed across a range of legal documents and agreements, and/or negotiate contracts with external partners, covering both Indonesia and Singapore jurisdictions.
Apply relevant laws and regulations in Indonesia and Singapore in day-to-day operations, including legal review, user/stakeholder advisory, and consultation to management.
Conduct legal research pertaining to the company’s business operational activities to ensure the company is up-to-date with the latest legal and regulatory developments.
Develop and implement legal procedures, policies, and workflow management systems, including proper documentation and archiving to ensure all legal documents are well-organized and easily searchable (e.g., via Google Drive, Notion).
Manage and collaborate with external law firms or legal counsel to support business needs effectively.
Represent the company in legal proceedings, working with outside counsel when required.
Bachelor’s degree in law (having a master's degree is an advantage).
5-8 years’ experience as a corporate lawyer at a reputable private practice firm and/or in-house legal.
Strong understanding of business processes and ability to act as a strategic business partner in translating cross-departmental needs into legal solutions.
Demonstrable legal analytical skills, strong business acumen, and sound judgment in decision-making.
Excellent legal drafting and writing skills (both in Bahasa Indonesia and English), with the ability to simplify complex legal matters for non-legal stakeholders.
Proven experience in advising senior management and leadership team, including providing practical and actionable legal recommendations.
Ability to manage multiple priorities, structure workflows, and ensure proper documentation and archiving systems (e.g., Google Drive, Notion).
Strong project management skills with attention to detail and accuracy.
Strong interpersonal and influencing skills to work well within the legal team and internal/external stakeholders.
Lead the implementation, maintenance, and continuous improvement of the Company’s Quality Management System (QMS), including ISO 9001, ISO 17025, ISO 13485, and ISO 15189 scopes as required by business needs.
Ensure effective document and record control through the Document Management System (DMS), including SOPs, policies, forms, and quality records.
Oversee quality assurance processes including risk management, change control, deviation handling, CAPA management, and internal audit programs to ensure compliance and process consistency.
Ensure compliance with applicable regulations, quality standards, and customer requirements, and maintain readiness for internal and external audits.
Coordinate with regulatory bodies, certification agencies, auditors, and clients regarding audits, inspections, and corrective action follow-ups.
Monitor and analyze Quality KPIs, non-conformities, audit findings, and improvement initiatives to support management review and decision-making.
Collaborate with cross-functional teams to ensure quality requirements are effectively implemented across company operations.
Lead and develop the QA team through performance management, competency development, coaching, and training programs.
Drive continuous improvement initiatives to enhance quality systems, operational efficiency, and compliance effectiveness.
Bachelor’s degree in Biology, Biomedical Science/Engineering, Pharmacy, Chemistry, Chemical/Industrial Engineering, or other related disciplines.
Minimum 4 years of experience in Quality Assurance, Quality Management System, or laboratory operations, with at least 2–3 years in a supervisory or lead role.
Experienced in implementing and maintaining ISO 9001 and/or ISO 17025 systems, including audit preparation and certification processes.
Familiar with regulatory licensing and compliance requirements under relevant government institutions such as the Ministry of Health and other related authorities.
Good understanding of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and risk-based quality management principles.
Proficient in Google Workspace (Sheets, Docs, Slides) and/or Microsoft Office (Excel, Word, PowerPoint), and familiar with project management or quality management tools.
Strong leadership, communication, interpersonal, and coordination skills, with the ability to work effectively in a cross-functional environment.
Highly organized, detail-oriented, proactive, and able to manage multiple priorities effectively.
Possess strong analytical thinking and problem-solving skills.
Demonstrate high integrity, honesty, and accountability in daily work activities.
Only shortlisted candidates will be contacted.
Jakarta
14 September 2026
1
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Manufacturing Biotechnologist
Looking for
S1
Executing production activities and preparing production reports in a strict adherence to Standard Operating Procedures.
Ensuring all workplace activities comply with Standard Safety and Quality guidelines.
Drafting and updating Work Orders (WO), forms, and other documents related to the document management system, particularly within the Technical Operations scope.
Occasionally carrying out research and additional inspections related to improvements in production processes, products, or analytical methods, with the aim of enhancing the quality, safety, and efficiency of products or operational processes.
Bachelor's degree in Biology, Pharmacy, Chemistry, Chemical/Industrial Engineering, or other related fields.
Experience in laboratories related to molecular biology, especially micropipette handling. Fresh graduates are welcomed to apply.
Experience in Laboratory Operations, as well as Quality and Laboratory Management Systems and molecular biology techniques, is a plus.
Demonstrates high integrity, honesty, a dynamic attitude, and excellent attention to detail. Experience with GMP, GLP, CPAKB, ISO 9001, ISO 13485, and ISO 17025 is a plus.
