Associate Director, Process Engineering, Synthetic Molecule Process Development (SMPD)

募集要項

仕事内容

Accountabilities：

Leads and manages a group of Engineers, providing technical guidance, mentoring, and performance management to ensure the team's success and professional growth.

Develops project and/ or significant technical strategy and leverages technical skill(s) as a resource/expert within the department.

Collaborates closely with cross-functional teams, including process chemistry, analytical development, drug product development, manufacturing, quality assurance, and regulatory affairs, to develop and implement effective process engineering strategies.

Drives process optimization initiatives to improve sustainability, process efficiency, yield, quality, and cost-effectiveness, utilizing expertise in process chemistry and fundamental engineering principles.

Oversees process scale-up activities from laboratory to pilot plant and commercial-scale production, ensuring smooth technology transfer and process validation.

Has full accountability for all engineering aspects for multiple pipeline projects.

Initiates complex projects with extraordinary technical challenges and applies strong technical risk assessment skills.

Owns a discipline/technical skill in its entirety and continues to develop expertise in other key technical skills.

Contributes significantly to develop, drive and set the vision and direction of departmental activities, management of resources, time, personnel and financial resources. Maintains ownership of overall vision of scientific platform.

Communicates and coordinates implementation of technology/scientific improvement to senior management, across therapeutic and scientific areas.

Conducts analysis of technical and conceptual risk through robust process characterization, failure mode analysis, and risk assessment methodologies, identifies trends and defines and champions process or scientific strategies.

Incorporates novel manufacturing, technologies and industry trends as a key aspect of scientific strategy development.

Maintains complete technical responsibility for program(s)/initiative(s) within the department.

Leverages cross functional knowledge to guide pharmaceutical sciences teams on potential impact of actions across projects, particularly in technical aspects.

Ensures effective project management of all plans and projects within area of responsibility, linking all scientific efforts to company, program and functional goals.

Leads small working groups as appropriate to address knowledge gaps in programs linking departmental strategy to strategies of other relevant functions.

Identifies topics for initiatives and leads local/global initiatives on behalf of senior staff.

Recognized as a technical leader/resource by the group and fosters development of technology skill sets within department and among junior staff.

Contributes to departmental strategy around scientific improvement and new capabilities.

Makes proposals regarding sourcing/consultancy strategy.

Coordinates and leads technology transfer to internal or external manufacturing sites or vendor

Communicates with senior management of other functions on implementation of infrastructure, technology, work processes, or business processes.

Responsible for authoring relevant sections of regulatory documents, validation plans, development reports, process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), process descriptions and peer reviewed manuscripts.

Defines outsourcing strategy for department in conjunction with senior staff.

Proactively identifies vendors and builds relationships to gain access to technologies as needed to deliver against pipeline goals.

Manages key vendor relationships across multiple projects as appropriate, and proactively affects resolution of issues arising at vendors.

Represents and is an active member on pre-competitive collaborations with academic and industrial partners.

経験・資格

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Education and Experience:

Required:

A Ph.D. degree with academic or pharmaceutical industry experience; an MS degree with pharmaceutical industry experience; or a BS degree with pharmaceutical industry experience. Degrees in chemical engineering required

Extensive experience in the use of mathematical, both statistical and first principle, models as well as advanced process control systems preferred.

Extensive experience in building reaction kinetic models as well as process models preferred.

Extensive experience in building laboratory and pilot plant equipment preferred.

Experience in crystallization process development and scale-up with an emphasis on polymorph, purity and particle size control a plus.

Experience in the use and scale-up of milling technologies (both dry and wet) for particle size control preferred.

Experience managing staff preferred.

Experience in the use of process analytical technologies (FT-IR, NIR, FBRM, UV-vis, etc.) required.

Experience in building chemometric models preferred.

Experience in developing continuous processes a plus.

Sound knowledge of current Good Manufacturing Practices (cGMP).

Experience working in a pilot plant a plus.

Previous experience with the use of contract facilities and managing technical transfers.

Experience in working in a multi-disciplinary team environment.

Significant technical and strategic leadership and accomplishments

Previous experience contributing to regulatory filings, preferably experience will late stage filings.

Proven scientific track record through presentations at scientific conferences and publication of pier reviewed manuscripts.

Knowledge and Skills:

Analytical and Problem Solving Skills - Able to troubleshoot critical issues or problems using appropriate information and, determine causes and possible solutions

Teamwork -- Ability to work well on global cross-functional teams.

Communication Skills -Able to express oneself clearly and concisely within team; documents issues and/or concerns concisely with colleagues; adjusts communication style as appropriate for the audience; timely and effectively communicates with senior management; technical writing skills to support authorship and approval of internal technical documents

Organization - Exercises good time management and prioritization skills to balance multiple project and departmental objectives

Technical - Subject matter expertise in a specific scientific area or areas. Demonstrated ability to successfully contribute across multiple scientific endeavors

Knowledge Sharing - Ability to capture knowledge within the organization; improves solutions, processes, and deliverables through use of information; improves information capital by contributing experience, theories, deliverables, and models for others to use

Resource Management -Project management skills; ability to manage one’s time within individual, departmental, and corporate goals and timelines; management of internal and external resources (vendors)

External Involvement - Demonstrated involvement in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events. Interacts with external vendors for projects

Leadership Skills - Develops and uses knowledge and interpersonal skills to appropriately influence and guide others towards the accomplishment of department/function goals and objectives.

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勤務地

神奈川県藤沢市

Recruiting No.

02000762000788

企業情報

社名

国内大手製薬メーカー

事業内容

医薬品の研究開発・製造・販売