Analytical Development Manager

**The Opportunity**

Esco Lifesciences Group provides enabling technologies, products and services to the life sciences and healthcare industries, supporting academic research and scientific discoveries, clinical practice, as well as biopharmaceutical R&D and manufacturing. Headquartered in Singapore, Esco has an extensive sales network in over 100 countries, direct sales and service offices in over 24 countries, 8 manufacturing and R&D hubs in the US, Europe, the UK, China, Singapore, Indonesia, and over 1500 employees worldwide.

Esco is poised to benefit from the sustained growth of the healthcare and biopharma industries in Asia and globally. Esco has achieved market leadership in China, and globally, in multiple categories within some of the fastest-growing segments — with China being its largest and fastest growing market. As a Singapore-headquartered company, Esco is a nexus of East and West, bridging technologies, products and talent across the world, with global operations spanning the US, Europe and Asia.

**Who we’re looking for**

**Physical/Mental Requirements/Work Environment**
- Ability to read, analyze and interpret scientific data and publications.
- Ability to author or review protocols, technical reports and technology transfer documents.
- Ability to author or review standard operating procedures and other related documents.
- Ability to define problems, collect data, establish facts, and draw conclusions.
- Ability to focus.
- Repetitive motions due to certain laboratory techniques.
- Ability to adapt and keep up with rapid changes in a fluid and dynamic environment as this is a rapidly evolving space.

**The Scope**

Primary work location: Ayer Rajah Crescent, Singapore.

**Responsibilities**:

- To conduct experimental procedures to establish, optimize and qualify analytical methods for in-process control samples and for product release.
- To participate in new product technology transfer, and lead assay qualification and validation activities.
- To support the technology transfer of analytical methods to downstream teams, such as QC department or applicable operating department, including provision of necessary training.
- To prepare high-quality technical protocols, reports, summaries, and quantitative analysis, for dissemination to project teams, and for regulatory agency submissions.
- To interface with regulatory and testing organizations to achieve projects deliverables within the specified timeline.
- To perform analysis of experimental data using statistical approaches.
- To work collaboratively with other groups to ensure Analytical Development activities are fully supported and aligned with other functional groups such as Process Development, Drug Product Development and Quality Assurance.
- To provide expertise to support function scientists, third parties, and other functions, to achieve the project goals and priorities.
- To troubleshoot, propose and implement resolutions to technical problems/issues.
- To write and maintain accurate, complete, and timely data in laboratory notebooks and experimental records.
- To develop new related analytical methods or improve current methods.
- To provide expertise and support other departments to achieve project milestones.
- To exercise scientific creativity and independent thought in research & process development.
- To perform tasks in accordance with applicable regulations and site safety requirements.
- To undertake other tasks as assigned based on project needs.

**Requirements**:

- PhD with 2-4 years of experience or a Masters/Bachelor degree with 4-8 years of experience in Biochemistry, Immunology, Molecular Biology or similar discipline.
- Experience with development of molecular assays for biological/vaccine products.
- Possess strong practical knowledge of molecular biology techniques such as RT-PCR, qPCR and/or NGS. Strong experience with flow cytometry is a plus.
- Familiarity with biological assays (Western blotting, SDS gels, PCRs, ELISA, protein assays etc) and analytical techniques (UV/IR/Raman Spectroscopy, HPLC, LCMS) is desired. Strong experience with flow cytometry is a plus.
- Experience in a GMP quality control environment preferred.
- Experience in analytical and QC testing of biologics is desirable.
- Previous experience with statistics and assay variability analysis, as applied in an industrial biopharmaceutical environment will be a distinct advantage.
- Experience with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) will be an advantage.
- Ability to plan and perform experiments in an interdisciplinary environment independently and efficiently.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently, self-starter, self-motivated and task oriented.
- Excellent written and verbal communication skills.
- Strong team player, develop positive relationship with a strong set of interpersonal skills.
- During the start-up phase of the teaM/Facil