Career

The Role

As the Chief of Staff of the company, this role will be closely working with the Management  Team and proactively managing and contributing to the company's strategies, and growth  initiatives i.e R&D strategies, financing, commercialization strategies, critical project  management; building

relationships with key stakeholders internally and externally to  achieve desired outcomes and deliverables.

Main Responsibilities and Duties：

Lead the development of understanding of industry trends and the competitive  landscape, perform quantitative and qualitative analysis on core strategic issues,  and generate outputs for executive feedback and approval. He/she should focus on identifying key value-added initiatives for Full-Life’s growth through a solid understanding of biotech business with a comprehensive view and strength in  business analytics. e.g., help the company to develop in-depth understanding on radiopharmaceutical market worldwide and gain insights into the market size, future  trends, key players, government policies; evaluate global radiopharmaceutical new product pipeline/technology and identify high priority opportunities, provide actionable business recommendations enabling management team to make  informed decisions.

Support CFO to connect with VCs and Funds to support the subsequent rounds of  financing.

Support CFO and Management Team to connect with external partners for potential  M&A or partnership.

Consolidate cutting-edge technology and market information, evaluate on market  trends, key players’ strategies, new initiatives, identify new opportunities to drive  business growth.

Collaborate with BD team and pro-actively scout potential partnerships to enrich  company’s capabilities。

Align with R&D team on company product portfolio strategy and priorities, identify  best practices from a portfolio management perspective from within and outside,  and surfacing opportunities for improvement。

Drive and track on company strategic project implementation.

Qualification

Ph.D. or MSc. in Bio/ Chem/ Pharma Science or related discipline.  

At least 2 years related experiences in management consulting, BD, investors or inhouse strategic role within Pharma industry and 5+ years working experience in  Pharma industry, additional biotech strategic planning experience is a plus.

A strategic thinker who can quickly understand new market trend and its driving  forces.

Extensive strategic project management and implementation experience.

Strong logical abilities, data sourcing and analysis skills, able to deliver reports.

Excellent communication and interpersonal skills, fluent both in English and  Chinese, work in cross-cultural work environment.

Good team player, work efficiently in matrix environment.

The Role

The radiochemist is responsible for providing contribution to the radiochemistry of Full-Life products, to support research, lead scaleup and automation of processes, and enhance capabilities in radio-labelling and radioanalytical measurements and separations.

Main Responsibilities and Duties :

Develop, review, conduct and interpret pharmaceutical and chemical production procedures for use in preclinical and clinical studies.

Provide technical support (or source appropriate advice) to radiochemistry and radiopharmaceutical process development and new product implementation.

Lead the planning, coordination and active management of all radiochemistry and radiopharmaceutical activities conducted by external vendors as analytical method qualifications,analytical method validations, technology transfers, manufacturing process validations.

Management of complex projects, including overall planning of experimental progress, identification and effective resolution of potential problems, tracking of project progress and ensuring timely and high-quality completion of projects.

Review technical content of regulatory documents for IND’s, IMPD’s and other regulatory submissions.

Manage outsourced activities and tracking of expenditure to ensure delivery on time and budget.

Ability to work closely with multiple company departments to ensure successful completion of projects.

Qualification

Master or PhD in chemistry, organic chemistry, medicinal chemistry or relevant discipline with knowledge of organics synthesis, peptide synthesis and ADC.

Strong knowledge of chemistry and analytical skills (including HPLC, ITLC, GC and radiometric assays)

Proven ability to effectively manage technical projects conducted by external vendors and contract manufacturers.

Experience in radiochemistry is preferred (preferrable with experience in commercial drug development and production)

Proven ability to multitask and coordinate parallel activities in a busy drug development program.

Forward-thinking, proactive, and creative. Natural problem-solver and team player.

The Role

The Program Management organization is the strategic backbone of F-L global R and D and MFG ; The Project Manager (PM) role within China organization has a great degree of impact on the business results that comes with matching accountabilities. She/he will cover projects of various scopes including pipeline monitoring, product development, continuous improvement, and large-scale strategic initiatives. And serve as a liaison between line managers, project teams, and management, as need. She/he will be a globally oriented innovator with ability to work across continents at the highest levels of innovation.

Main Responsibilities and Duties :

Adapt scientific knowledge to plan, design, conduct and interpret studies for target discovery and lead analysis.

Implement, coordinate and active manage of all activities to achieve the set goal through cooperation of external vendors and research collaborators and ensure delivery on time and budget.

Review technical content of regulatory documents for IND’s, IMPD’s and other regulatory submissions.

Keep a thorough understanding of cutting-edge science in potential target discovery and lead analysis to constantly improve relevant skills.

Contribute to regular project meetings and providing verbal or written feedback to inform the team or management of progress.

Qualification

5+ years’ working experience with Master Degree or relevant background

Experience in project management regards to biologics in CRO or Biotech setting (Preferrable with experience on ADC development)

Demonstrated track record or know-how for IND registration with NMPA (Preferrable with experience on oversea regulatory authority ie TGA/EMA/FDA)

Proven ability to effectively manage technical projects conducted by external vendors and research collaborator.

Project management skills including contracting, budget tracking/control and timeline management.

Proven ability to multitask and coordinate parallel activities in a busy drug development program.

Effective communication and reporting with excellent Chinese and English written/presentation skills.

Forward-thinking, proactive, and creative. Natural problem-solver and team player.