Associate Director, Global Quality Business Operations

Remote, United States Full time
Quality Associate Director
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Otsuka Pharmaceutical Development and Commercialization, Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Associate Director, Global Quality Business Operations 

The Global Quality (GQ) Business Operations Associate Director is responsible for providing centralized oversight and coordination of strategic initiatives, resource planning, portfolio management, and program performance management across Global Quality. This role enables data-driven decision making by maintaining an integrated view of program priorities, resource capacity, dependencies, and initiative progress. The position serves as a key business partner within Global Quality, driving transparency, accountability, operational effectiveness, and continuous improvement while strengthening collaboration across global programs and strategic initiatives.

The Associate Director, GQ Operations will help build and mature program management capabilities, preserve organizational knowledge through process documentation and governance, and support the scalability of Global Quality operations to meet evolving business needs.

Key Responsibilities

Strategic Portfolio & Program Management

Lead the management of a consolidated portfolio view of Global Quality strategic initiatives, programs, and key projects, enabling informed prioritization, resource allocation, and investment decision-making.

Track initiative progress, milestones, risks, dependencies, and deliverables across Global Quality Operations global programs.

Designs and governs program management standards, tools, and reporting mechanisms to strengthen program management discipline, improve execution consistency, and build organizational capabilities across Global Quality.

Facilitate governance reviews and provide regular updates on program performance across Global Quality Operations

Continuous Improvement & Performance Monitoring

Enable performance monitoring through the development and maintenance of metrics, dashboards, and reporting processes that provide visibility into operational effectiveness.

Drive action tracking, follow-through, and accountability to support the timely execution of commitments, deliverables, and strategic priorities.

Utilize performance data, trends, and insights to identify opportunities for operational effectiveness, process optimization, and continuous improvement.

Support governance activities, performance reviews, and operational assessments to drive proactive decision-making and sustained improvement across Global Quality.

Process Governance & Knowledge Management

Maintain end-to-end process maps, operational documentation, and process ownership frameworks.

Ensure process documentation remains current, accurate, and aligned with organizational objectives.

Promote program best practices across Global Quality.

Preserve organizational knowledge and reduce dependency on individual expertise through robust documentation and governance practices.

Stakeholder Partnership & Collaboration

Strengthen engagement and collaboration between Global Quality and functional business partners through the Centers of Excellence.

Foster strong cross-functional partnerships to support alignment on strategic priorities, initiatives, and organizational objectives.

Facilitate effective communication and coordination across regions, programs, and stakeholder groups to promote shared understanding and execution.

Enhance transparency of priorities, dependencies, risks, and outcomes to support informed decision-making and organizational alignment.

Act as a strategic partner to Global Quality leadership, Global Quality Operations, and business stakeholders to drive operational effectiveness and successful delivery of strategic initiatives. .

Qualifications 

Bachelor’s degree required; advanced degree in Business Administration, Operations Management, Quality, Life Sciences, or a related field.

8+ years of experience in portfolio management, strategic planning, PMO leadership, business operations, or organizational effectiveness

Experience in program management, portfolio management, business operations, strategic planning, operational excellence within pharmaceutical, biotechnology, healthcare, or other regulated industries.

Demonstrated ability to manage multiple strategic initiatives and priorities within a complex, global organization.

Experience developing and maintaining portfolio management processes, governance frameworks, project plans, and operational reporting mechanisms.

Experience developing metrics, dashboards, and performance reporting to support leadership decision-making and operational effectiveness.

Experience facilitating cross-functional collaboration and stakeholder alignment across business functions, regions, and global programs.

Knowledge of process improvement methodologies, operational excellence principles, and organizational effectiveness practices.

Experience tracking program performance, risks, dependencies, actions, and deliverables to drive accountability and execution discipline.

Strong analytical skills with the ability to synthesize data, identify trends, and provide actionable business insights.

Excellent organizational, communication, presentation, and stakeholder management skills.

Key Competencies

Strategic thinking and business acumen

Program and portfolio management

Resource planning and prioritization

Data analysis and performance management

Process mapping and governance

Continuous improvement mindset

Stakeholder engagement and influence

Cross-functional collaboration

Executive communication and presentation skills

Organizational change and transformation support

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.

Minimum $150,034.00 - Maximum $224,250.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

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://ah-prod.com/multi/videoplayer/player.html?v=6385356920112 .

Join Our Talent Community: Stay connected with Otsuka by joining our Talent Community. Tell us about your interests, and we’ll notify you about future opportunities that align with your background. https://community.hireez.com/cielo-otsuka/82cb3591

Disclaimer: 

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 EEAccommodations@otsuka-us.com .

Statement Regarding Job Recruiting Fraud Scams

At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives.  They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.

Please understand, Otsuka will never ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.

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To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External .

Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka’s call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov ,  or your local authorities.

Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. (“Otsuka”) does not accept unsolicited assistance from search firms for employment opportunities.  All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka’s application portal without a valid written search agreement in place for the position will be considered Otsuka’s sole property.  No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Job details

Seniority
Associate Director
Function
Quality
Therapeutic area
Not listed
Location
Remote, United States
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 456 comparable Associate Director Quality roles across 92 biopharma companies.

456Comparable roles tracked
408Currently active
92Companies hiring similar roles
41Countries represented

Salary context

84 of 456 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Highest disclosed · Assoc Director, Quality Assurance · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $66,560 – $208,845 (median $143,350)

Where these roles are based

Top locations among the 456 comparable roles

United States189
Ireland36
China32
India24
United Kingdom21
Germany17

+ 35 more countries

Seniority mix

456 of 456 peers have a known seniority level

Manager223
Senior189
Associate Director44

Therapeutic area mix

1 of 456 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Biogen Cambridge, United States Associate Director
Same function Same seniority Same country
60%similar
Devens Devens, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country
60%similar
Otsuka Pharmaceutical Development and Commercialization, Inc. Remote, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Quality job in the United States, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Director, Global Quality Risk Management
Biogen · Cambridge, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, GMP Operational Quality (Biologics and Devices)
Vertex Pharmaceuticals Inc (US) · Boston, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Quality Control - Technical Services
Vertex Pharmaceuticals Inc (US) · Boston, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Senior Device Quality Engineer Associate Director
GlaxoSmithKline LLC · Upper Providence, United States · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.