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Senior Director, External Manufacturing
Johnson & JohnsonSenior Director responsible for global external manufacturing strategy for biotherapeutics at Johnson & Johnson. Leading partnerships and ensuring compliance with quality and regulatory standards.
Posted 5/14/2026full-timeTitusville • New Jersey, Pennsylvania • 🇺🇸 United StatesSenior💰 $178,000 - $307,050 per yearWebsite
About the role
Key responsibilities & impact- Defining and executing global strategies for externally manufactured biotherapeutic drug products across launch and commercial supply.
- Providing leadership oversight for performance, risk management, and business continuity across the external network.
- Driving alignment between product strategy, network strategy, and enterprise priorities.
- Establishing and leading strategic, long-term partnerships with global CMOs.
- Ensuring effective governance, performance management, and issue escalation across external partners.
- Representing Johnson & Johnson as a senior leader in external manufacturing relationships.
- Ensuring consistent delivery against safety, quality, service, and cost objectives.
- Partnering with Technical Operations and Quality to enable successful tech transfers, lifecycle changes, and capacity expansions.
- Championing continuous improvement, digital enablement, and adoption of industry best practices across the external network.
- Ensuring full compliance with global cGMP requirements and Johnson & Johnson quality standards.
- Maintaining inspection readiness and proactive risk mitigation across all external manufacturing partners.
- Supporting regulatory interactions related to external manufacturing activities.
- Leading, coaching, and developing a high-performing external manufacturing leadership team.
- Serving as an active leader within the broader Manufacturing & Supply organization.
- Influencing senior stakeholders through clear, strategic communication and data-driven insights.
Requirements
What you’ll need- Bachelor’s degree in Engineering, Life Sciences, or related field (advanced degree preferred).
- Extensive leadership experience (typically 10+ years) in biotherapeutic manufacturing, with significant exposure to external manufacturing or CMO oversight.
- Deep knowledge of biologics manufacturing, technology transfer, lifecycle management, and global regulatory expectations.
- Demonstrated success influencing outcomes through cross-functional leadership in complex, global matrix organizations.
- Demonstrated people leadership experience, including leading teams and stakeholders through direct and matrixed reporting relationships.
- Preferred: Experience supporting late-stage and commercial biologics portfolios.
- Strong business and financial acumen.
- Proven ability to lead through complexity, ambiguity, and change.
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
ATS Keywords
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Hard Skills & Tools
biotherapeutic manufacturingtechnology transferlifecycle managementcGMP compliancerisk managementperformance managementcontinuous improvementdigital enablementregulatory interactionsexternal manufacturing oversight
Soft Skills
leadershipstrategic communicationinfluencing stakeholderscross-functional leadershipcoachingteam developmentbusiness acumenfinancial acumenproblem-solvingadaptability