Regulatory Affairs Principal Engineer

For over 170 years, Leica Microsystems has helped shape the future by developing groundbreaking optical and digital solutions. As a global leader, we’re driven by continuous improvement to excite our customers and to create the best work environment for our people. Customer focus, innovation, and teamwork are at the core of our culture and the foundation...

Job Summary:We are seeking a highly experienced Regulatory Affairs Specialist to join our team at JUNION LABS PTE. LTD. The successful candidate will have a strong background in FDA regulations and experience with drug development and registration.The Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies for...

**Location** - Singapore, East**Job Type** - Permanent**Salary** - $7,000 - $14,000 Per Month**Date Posted** - 5 hours agoAdditional Details **Job ID** - 99804**Job Views** - 1Roles & Responsibilities **Key Job Purpose**: - Dossier preparation & product registration submission to HSA, leading to timely introduction of new products and responsible for...

**Position Snapshot** Location: Singapore Company: Nestle R&D Center, Singapore Type of contract: Permanent **Position Summary** Joining Nestlé means you are joining the largest Food and Beverage Company in the world. At our very core, we are a human environment - passionate people driven by the purpose of enhancing the quality of life and contributing...

At **Epista**, we are redefining what excellence looks like in the life science industry. As trusted advisors to some of the world’s leading pharma, biotech, and medtech companies, we combine regulatory insight with deep domain expertise to drive performance. Our mission? To **define and deliver process, technology, and compliance excellence**—empowering...

Roles & Responsibilities Key Responsibilities Regulatory Strategy Develop and implement regulatory strategies for U.S. drug approvals (IND, NDA, etc.) in alignment with company objectives.Provide expert advice on FDA regulations, guidance documents, and best practices to cross-functional teams (R&D, Clinical, Quality, Manufacturing). Submission Management...

Roles & ResponsibilitiesKey Responsibilities Regulatory Strategy Develop and implement regulatory strategies for U.S. drug approvals (IND, NDA, etc.) in alignment with company objectives.Provide expert advice on FDA regulations, guidance documents, and best practices to cross-functional teams (R&D, Clinical, Quality, Manufacturing). Submission Management...

With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced CMC Regulatory Affairs Associate Director to join the Autolus team to work on innovative and pioneering products across Autolus’ cell and gene therapy portfolio. The Regulatory Affairs Associate Director will be part of the CMC regulatory affairs team with...

Regulatory Affairs Expert:We are seeking a highly experienced Regulatory Affairs Expert to join our team at JUNION LABS PTE. LTD. The successful candidate will have a strong background in FDA regulations and experience with drug development and registration.The Regulatory Affairs Expert will be responsible for developing and implementing regulatory...

**Job Summary**: - To supervise the activities of scientific and operational staff responsible for method development/validation projects and analysis of samples. - Serves as Principal Investigator for research studies. Take on overall responsibility for the technical conduct of a study, analytical direction, review, documentation and reporting of...

Leica Microsystems has helped shape the future of microscopy for over 170 years by developing groundbreaking optical and digital solutions. As a global leader, we’re driven by continuous improvement to excite our customers and to create the best work environment for our people. Customer focus, innovation, and teamwork are at the core of our culture and the...

Roles & ResponsibilitiesBring more to life.Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Leica Microsystems, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.You'll thrive in a culture of...

To perform and supervise the activities of scientific and operational staff responsible for method development/validation projects and analysis of samples. - Serves as a Study Director / Principal Investigator / Responsible Scientist for research studies. Take on overall responsibility for the technical conduct of a study, analytical direction, review,...

Job ID: **ENG-SITE-PLANNING** **Job Type**: **Full Time** Job Classification: **Assistant / Manager** Department: **Engineering** Function: **Engineering** **Location**: **Jurong, Singapore** Years of Experience: **3** Job Responsibilities/Requirements: **Responsibilities**: - To acquire premises’ Mobile Installation Space (MIS), including HDB...

1. Process mechanical engineering CD plans 2. Conduct regulatory site inspection 3. Provide CD specialist engineering advice **_Responsibilities _** - You will process mechanical engineering CD plans (ACMV, Plumbing & Sanitary and Fire Protection Systems) of Civil Defence shelters in MRT stations submitted by consultants, conduct regulatory off-site and...

**General Manager**: **Responsibilities** 1. Develop and implement the strategic business plan. 2. Develop rapport and work with SSG, CPE and related government agencies to develop short and mid-term strategies. 3. Manage the Institute’s business and operation in compliance with SSG’s CPE’s and PDPC’s requirements. 4. Manage the Institute's...

**About us**: At DHL, people mean the world to us. That’s why our goal has always been to attract and retain the best talent over the world. We provide challenge and opportunity for personal and professional development. We recognize the difference you bring to our business, and together we share the pride of building THE logistics company for the...

**Responsibility**: - Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: - entry of safety data onto adverse event database(s) and tracking systems - review of adverse events for completeness, accuracy and appropriateness for expedited...

Roles & ResponsibilitiesJob Summary: The Regulatory Affairs & QA Executive is responsible for ensuring compliance with local and international food safety regulations, managing regulatory submissions, and supporting quality assurance initiatives. This role involves coordinating with internal teams to maintain regulatory compliance, supporting product...

**About Lubrizol** **ACCOUNTABILITY**: To influence government authorities & officials and trade associations to advance Lubrizol's business strategies and goals, and ensure Corporate Social Responsibility (CSR) governance to comply with Lubrizol’s guidelines on charitable donations and align with corporate standards and requirements in Asia...