Biotherapeutics Study Director, Pharma Discovery, New Taipei City

  • Wugu District, New Taipei City, Taiwan 248
  • Full-time

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 55,000 staff across a network of more than 1000 independent companies in over 50 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.  In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

1.     Develop method and perform testing on large molecule drug candidates using mass spectrometry, HPLC/UPLC, CE, SPR, and DSF

2.     Draft experiment SOP and ensure accurate data management and reporting with the highest integrity; manage quality control on project data and reports

3.     Take ownership of research projects with minimal supervision

4.     Develop client and stakeholder relationships through technical leadership and collaboration

5.     Support client service team in generating proposals, study plans and scope of work. Assists pricing team in completing custom pricing and cost analysis

6.     Manage client projects in all phases of study life cycle, from study design to reporting

7.     Provide training to colleagues and external end users

8.     Perform other duties as assigned

9.     Flexible on working hours and working day schedule

Required skills:

1.     Experience in drug discovery process and biophysical assessment of large molecules

2.     Scientific expertise in biophysical assessment of large molecules, such as mass spectrometry, HPLC/UPLC, CE, SPR, and DSF

3.     Experience in qualifying and maintaining equipment used in biophysical assays

4.     Ability to trouble-shoot technical problems and literature research on the relevant publication

5.     Experience in drafting and executing equipment and method validation in a non-GLP environment

6.     Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations

7.     Experience in CRO business and abilities to develop client relationships, support technical correspondence, and present scientific proposals to clients are highly desirable

8.     Ability to support project management, plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources

9.     Experience with leading and influencing effective cross-functional team collaboration, including lab operations, business development, marketing, and outsourcing stakeholders

Qualifications

1.     Experience in drug discovery process and biophysical assessment of large molecules

2.     Scientific expertise in biophysical assessment of large molecules, such as mass spectrometry, HPLC/UPLC, CE, SPR, and DSF

3.     Experience in qualifying and maintaining equipment used in biophysical assays

4.     Ability to trouble-shoot technical problems and literature research on the relevant publication

5.     Experience in drafting and executing equipment and method validation in a non-GLP environment

6.     Excellent interpersonal, verbal and written skills, including ability to prepare detailed scientific reports and group presentations

7.     Experience in CRO business and abilities to develop client relationships, support technical correspondence, and present scientific proposals to clients are highly desirable

8.     Ability to support project management, plan and coordinate multiple projects simultaneously, with appropriate allocation of available resources

9.     Experience with leading and influencing effective cross-functional team collaboration, including lab operations, business development, marketing, and outsourcing stakeholders

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