Senior Manager, Biologics Analytical Development (CMC Attribute Science)
The Senior Manager, CMC Data Analytics is responsible for Executing and supporting data-driven integration, analysis, and interpretation of CMC data to support biologics development from IND-enabling studies through BLA submission and commercialization.
This role serves as a CMC analytics subject matter expert (SME) who partners across Analytical Development, Process Development, MSAT, Quality, and Regulatory Affairs to analyze, summarize and process datasets into clear regulatory narratives, risk-based control strategies, and informed CMC decisions. The position plays a critical role in ensuring data quality, consistency, traceability, and regulatory readiness for global filings.
Key Responsibilities:
- Execute and support integration, analysis, visualization, and interpretation of CMC data across development stages (early, late, and commercial).
- Aggregate and trend analytical, process, stability, and comparability datasets to support CMC decision-making and regulatory strategy.
- Apply statistical and scientific approaches to evaluate variability, trends, and comparability across manufacturing changes and lifecycle events.
- Translate complex CMC datasets into clear, defensible conclusions for internal governance and regulatory submissions.
- Partner with Analytical Development to interpret method performance, lifecycle data, and validation outcomes in a CMC context.
- Collaborate with Upstream, Downstream, and MSAT teams to link process performance with product quality attributes.
- Provide analytical data and insights to support control strategy development..
- Perform data analysis to support comparability assessments under guidance for process changes, scale-up, site changes, and technology transfers.
- Review and support evaluation t of CMC data generated by CDMOs and external testing laboratories.
- Review external reports, datasets, and summaries to ensure scientific accuracy and regulatory fitness.
- Support data transfers and reconciliation activities during tech transfers and manufacturing transitions.
Qualifications
Education
- M.S in Analytical Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, Engineering, or related discipline
Experience:
- 8 – 10 years of Demonstrated experience supporting IND and BLA submissions, with direct involvement in data presentation and regulatory narratives.
- Proven track record applying CMC data analytics to support comparability, control strategies, and regulatory filings.
Technical Expertise
- Strong understanding of analytical methods and data types used in biologics CMC (e.g., purity, potency, identity, stability).
- Experience with statistical analysis, data trending, and visualization in a regulated environment.
- Solid knowledge of regulatory expectations for CMC data integrity, traceability, and lifecycle management.
Competencies
Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
Empowered Development - Play an active role in professional development as a business imperative.
Application Deadline: This will be posted for a minimum of 5 business days.
Company benefits: Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; https://www.otsuka-us.com/careers-join-otsuka.
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request.
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Skills Required
- Master's degree in Analytical Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, Engineering, or related discipline
- 8-10 years supporting IND and BLA submissions with direct involvement in data presentation and regulatory narratives
- Proven experience applying CMC data analytics to support comparability, control strategies, and regulatory filings
- Strong understanding of analytical methods and data types used in biologics CMC (purity, potency, identity, stability)
- Experience with statistical analysis, data trending, and visualization in a regulated environment
- Knowledge of regulatory expectations for CMC data integrity, traceability, and lifecycle management
- Experience reviewing and evaluating CMC data from CDMOs and external testing laboratories
- Experience supporting data transfers and reconciliation during tech transfers and manufacturing transitions
- Impactful communication and cross-functional collaboration skills for regulatory narratives and governance
Otsuka America Pharmaceutical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Otsuka America Pharmaceutical and has not been reviewed or approved by Otsuka America Pharmaceutical.
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Healthcare Strength — Health coverage spans medical, dental, vision, prescription services, telehealth, life insurance, and disability, with notable mental‑health access through therapy, coaching, and digital tools. Wellness resources such as fitness reimbursement, nutrition support, and caregiver assistance further reinforce overall healthcare robustness.
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Retirement Support — Retirement offerings include a strong 401(k) match alongside personalized financial counseling for tax planning, education funding, home buying, and estate planning. These features position retirement support as a differentiator within the total rewards package.
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Leave & Time Off Breadth — Time‑off policies include flexible time off, paid holidays, volunteer time off, and a company winter holiday break. The breadth of leave programs supports work–life balance across various needs.
Otsuka America Pharmaceutical Insights
What We Do
There are two Otsuka pharmaceutical industry companies in the U.S.: Otsuka America Pharmaceutical, Inc. (OAPI) successfully commercializes Otsuka-discovered and in-licensed products in North America. Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) clinically develops and registers innovative healthcare products on a global basis.






