Head of Process Chemistry, Synthetic Molecule Process Development応募後で応募 求人ID R0106275 掲載日 09/11/2023 Location:Cambridge, Massachusetts
About the role:
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.
The Process Chemistry (PC) group within Synthetic Molecule Process Development (SMPD) is responsible for the development and execution of robust and cost-effective processes for the manufacture of new synthetic molecule Drug Substance (DS), along with methods for achieving and controlling high standards of purity and quality, from hand-off from the Process Research team at Ph1 through PPQ and transfer to Commercial.
The successful candidate for Head Process Chemistry TMA group will manage his/her staff with accountability for performance and results including: the development and characterization of chemical processes with a focus on robustness, sustainability and COGS, technical transfer to manufacturing sites, oversight of cGMP manufacture, and representation on CMC teams. They will develop their staff to deepen their expertise in disruptive route scouting utilizing innovative synthetic approaches, subsequent process development and process characterization and PPQ support. As a leader within the global synthetic molecule process development department, the successful candidate will contribute his/her technical expertise across multiple sites and multiple teams, defining global best practices and maintaining and deepening our global expertise by benchmarking current industry trends in process chemistry and participation in industrial/academic consortia. He/she will also be expected to lead and drive both line function and cross-functional strategy and lead teams with accountability for performance and results.
Responsible for technical, budgetary, and development oversight of the PC group at the Takeda Massachusetts (TMA) site
Assure technical deliverables for DS projects under team direction (process development work captured in technical reports, tech transfer and cGMP productions, process characterization consistent with QbD principals, and process validation as appropriate)
Develops and manages strategies for process chemistry infrastructure, resources, projects, outsourcing, etc. in conjunction with local and global senior staff.
Serves as a technical resource to guide group members in strategic decision making and conducts analysis of technical and conceptual risk; identifies and champions operational processes and mitigation strategies.
Monitors and participates in establishing industry trends and recommends and implements new technologies and innovations to deliver upon process chemistry goals as appropriate.
Develops discipline/departmental plans/initiatives and drives strategy and implementation for process chemistry, creating linkages with strategies of other relevant functions.
Accountable for all aspects of department performance, personnel issues, and effective communication within group and with the company.
Provides technical/departmental leadership by fostering development of skill sets among staff, and providing guidance on project leadership and cross-functional awareness
Drives cross-departmental, R&D-level and cross-divisional strategy and identifies topics for initiatives and leads global department, cross-department, R&D-level and cross-divisional initiatives with accountability for performance and results. Communicates efforts with senior management of other functions as appropriate.
EDUCATION, EXPERIENCE AND SKILLS:
Education and Experience:
Bachelor’s degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science and 20+ years relevant industry experience
Master’s degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 18+ years relevant industry experience
PhD in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 15+ years relevant industry experience
Sound knowledge of current Good Manufacturing Practices (cGMP)
Significant relevant pharmaceutical development experience
Significant relevant experience with industrial/academic consortia establishing industry trends/best practices
Significant technical and strategic leadership experience with direct accountability for managing a team of direct reports
Experience leading in a multi-disciplinary environment with accountability for informing departmental or functional strategy.
Knowledge and Skills:
Resource Management - Project management skills and familiarity with financial aspects related to projects including ability to anticipate and manage internal and external resource needs (people, information, technologies, time, and capital)
Demonstrated ability to supervise team of employees, while fostering a positive/collaborative work environment.
Demonstrated ability to coach and mentor direct reports, identifying growth opportunities and supporting their professional development.
Analytical and Problem-Solving Skills - Able to troubleshoot the critical issues or problems and determine causes and possible solutions
Teamwork -- Ability to work well on and effectively lead global cross-functional teams
Communication Skills -Ability to expresses oneself clearly and concisely within team; documents issues and/or concerns concisely and comprehensively; adjusts communication style appropriate for the audience; timely and effectively communicates with senior management and direct reports; technical writing skills to support authorship of internal/external & approve internal technical documents
Organization – Exercises good time management and prioritization skills to balance a number of project and departmental objectives
Technical - Relevant expertise across a broad range of disciplines related to drug development
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
External Involvement – Involved in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events. Involvement in establishing and applying industry trends. Advises team members or directly interacts with external vendors for projects
LINE FUNCTION SPECIFIC QUALIFICATIONS:
PhD-level research in organic chemistry or related field; or substantial industrial organic chemistry lab-based research experience
Advanced proficiency with typical analytical tools (e.g. NMR, UV, IR, HPLC)
Proficiency with utilizing typical literature searching techniques to solve organic chemistry problems
What Takeda can offer you:
401(k) with company match and Annual Retirement Contribution Plan
Tuition reimbursement Company match of charitable contributions
Health & Wellness programs including onsite flu shots and health screenings
Generous time off for vacation and the option to purchase additional vacation days
Community Outreach Programs
Discover more at takedajobs.com
No Phone Calls or Recruiters Please.
This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote Work policy.
Base Salary Range: $198,100.00 to $283,000.00. Employees may also be eligible for Short Term and Long-Term Incentive benefits. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off.
The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience.
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.