Scientist/Senior Scientist, Analytical Development - Synthetic Molecules

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Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Scientist/Sr. Scientist, Analytical Development – Synthetic Molecules in our Cambridge office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Scientist/Sr. Scientist working on the Analytical Development – Synthetic Molecules team, you will be empowered to participate in cross-functional CMC teams and provide guidance to junior members of the Analytical Development.

Qualifications for a Senior Scientist/Scientist in Analytical Development for small molecules and middle molecules (oligonucleotide, peptide) include:

Strong knowledge of analytical techniques with advanced experience in multiple techniques such as LC, GC, CE, MS, dissolution, etc.; Able to work in lab setting; Experience representing Analytical Development in a cross functional CMC environment; Multiple experiences with methods development, validation, and transfer; Ability to design and direct analytical strategy to meet CMC project objectives.

POSITION OBJECTIVES:

Provides theoretical/conceptual input to the design, development and execution of research assignments for a specific project or projects within the functional area. Independently plans and executes most unit operation characterization and optimization experiments within expertise and develops an awareness of unit operations in other areas. Responsible for significant or sole technical leadership within project or complex study. Prepares technology transfer documentation and regulatory documents or coordinates with team members to ensure execution. Represents line functions on Global CMC teams as appropriate/necessary. Proactively identifies process or study issues/challenges and proposes potential resolutions.

POSITION ACCOUNTABILITIES:

• Understands project timelines and deliverables and plans/coordinates project work accordingly with departmental, functional and external stakeholders
• Provides technical leadership to project teams within area of expertise and commits resources to execute specific project tasks.
• Contributes significantly and independently to project work which may include multiple projects within functional area.
• Reviews, interprets and communicates data cross-functionally within CMC and project teams.
• Plans and implements resolutions to technical problems/issues
• Represents functional area on Global CMC project teams by communicating activities from designated functional area to project team
• Supports local and global initiatives which may include leading initiatives or work streams
• Serves as a technical resource for junior staff and leverages expertise in laboratory technology as a functional resource/trainer.
• Independently designs and executes experiments, and reports results
• Assists with development of project strategy and communicates complex data/decisions within department and cross functionally as necessary
• Builds and maintains relationships with key vendors and assists with technical aspects of vendor negotiations
• Proactively analyses manufacturing issues and coordinates potential resolution with the global CMC team.
• Responsible for integrating scientific/technical efforts around cross-functional issues

EDUCATION, EXPERIENCE AND SKILLS:

Education and Experience:

Required:

• Bachelors degree in chemistry, biology, pharmacy, or related pharmaceutical science and 11+ years (Sr. Scientist) or 8+ years (Scientist) relevant industry experience
• Masters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 9+ years (Sr. Scientist) or 6+ years (Scientist) relevant industry experience
• PhD in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 3+ years (Sr. Scientist) relevant industry experience
• Extensive experience in CMC pharmaceutical development for active pharmaceutical ingredients and drug products under cGMP’s
• Sound knowledge of current Good Manufacturing Practices (cGMP)
• Previous experience with the use of contract facilities
• Experience in working in a multi-disciplinary team environment

Knowledge and Skills:

• Strong knowledge of analytical techniques including experience using multiple techniques (LC, GC, Dissolution, MS, etc.) and advanced experience in at least one technique.
• Able to interpret results of complex experiments and integrate data produced by other disciplines.
• Able to work in lab setting.
• CMC experience; Methods development, validation and transfer preferred.
• Analytical and Problem Solving Skills - Able to troubleshoot critical issues or problems, and determine causes and possible solutions
• Teamwork -- Ability to work well in highly cross functional team environment and across global line functions.
• Communication Skills -Able to expresses one’s self 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 issues to supervisor; technical writing skills to support authorship of internal technical documents
• Organization – Exercises good time management and prioritization skills and is able to successfully manage multiple tasks simultaneously
• Knowledge Sharing - Ability to capture organizational knowledge; improve solutions, processes, and deliverables through use of information; improve information capital by contributing experience, theories, deliverables, and models for others to use
• Resource Management -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
• Technical - Subject matter expertise and knowledge of applicable lab equipment and operations

LOCATION AND TRAVEL REQUIREMENTS:

• On-site role in Cambridge, MA
• May require approximately 5-10% travel.

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

In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.

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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.