Director of Maintenance Wilmington, Biotech

MSD

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profile Job Location:

Wilmington, DE - USA

profile Monthly Salary: $ 169700 - 267200
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Job Description

Welcome to the Future of Precision Oncology Join Us in Wilmington DE!

Were thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington Delawarea bold step forward in transforming cancer care through innovation collaboration and purpose-driven science.

ADCs represent one of the most exciting frontiers in biopharmaceuticals today. By combining the targeting power of monoclonal antibodies with the potency of cytotoxic drugs ADCs deliver cancer-killing agents directly to tumor cells minimizing damage to healthy tissue. This precision has revolutionized treatment for hematologic malignancies and is rapidly expanding into other cancers. The global ADC market is booming projected to surpass $16 billion in 2025 and grow steadily through 2035. Innovations in linker technology payload design and AI-driven antibody optimization are accelerating breakthroughs and expanding therapeutic possibilities.

Our Wilmington facility is designed to meet the growing demand for high-potency manufacturing ensure supply chain resilience and support the next wave of ADC launches. Importantly this site will support both drug substance conjugation and drug product.

As a member of the Wilmington Biotech site leadership team the Director of Maintenance will lead and oversee all maintenance operations for our sterile product manufacturing facility. This role is critical in ensuring the reliability safety and efficiency of all equipment and systems while adhering to strict regulatory standards and best practices in the pharmaceutical industry. The ideal candidate will possess extensive experience in engineering and facilities management particularly in sterile environments and will demonstrate strong leadership capabilities to drive continuous improvement initiatives. This position will also have oversight and accountability for integrated facilities management (IFM) for the site.

Key Responsibilities:

Leadership & Strategy:

  • Develop and implement a comprehensive maintenance strategy aligned with the facilitys operational goals.
  • Lead and manage the maintenance staff fostering a culture of safety compliance and continuous improvement.
  • Oversee talent management processes including recruitment training performance evaluations and career development for maintenance personnel.
  • Collaborate with cross-functional teams to ensure maintenance activities support production schedules and compliance requirements.

Facilities Maintenance Operations:

  • Design and implement a comprehensive predictive and preventive maintenance program to improve asset reliability and manufacturing capacity.
  • Design and implement an integrated facilities management (IFM) program for the site.
  • Oversee all maintenance activities including preventive predictive and corrective maintenance for all equipment and systems.
  • Ensure compliance with Good Manufacturing Practices (GMP) safety regulations and environmental standards.
  • Manage maintenance budgets forecasts and resource allocation to optimize operational efficiency.

Continuous Improvement:

  • Drive initiatives to enhance equipment reliability and reduce downtime through root cause analysis and implementation of best practices.
  • Introduce and integrate reliability engineering principles into maintenance practices including RCM FMEA and Criticality Analysis.
  • Utilize predictive maintenance tools (e.g. vibration analysis ultrasound infrared thermography) to assess asset condition and optimize maintenance activities.
  • Lead projects related to equipment upgrades installations and process improvements employing Lean manufacturing principles to streamline operations.

Regulatory Compliance:

  • Ensure all maintenance practices comply with FDA regulations ISO standards and internal policies.
  • Prepare for and participate in regulatory inspections and audits providing necessary documentation and evidence of compliance.
  • Promote a culture of safety within the maintenance team ensuring adherence to safety protocols and practices during maintenance operations.

Collaboration & Communication:

  • Serve as the primary point of contact for maintenance-related issues collaborating with production quality assurance and engineering teams.
  • Communicate maintenance strategies goals and performance metrics to senior management and stakeholders.
  • Prepare and present regular reports on maintenance performance reliability metrics and improvement initiatives to senior management.

Minimum Education and Experience:

  • Bachelors degree in Engineering Facilities Management or a related field with ten (10) years of experience in maintenance management within a pharmaceutical or biotech environment

Required Skills and Experience:

  • At least five (5) years in a leadership role.
  • Proven experience in managing maintenance for sterile manufacturing processes and equipment.
  • Experience demonstrating leadership and technical skills in high-pressure environments.
  • Experience or training in Lean manufacturing methodologies with a track record of implementing Lean principles to improve maintenance processes and operational efficiency.
  • Strong knowledge of maintenance management systems (CMMS) and reliability-centered maintenance practices.
  • Excellent leadership communication and interpersonal skills.
  • Ability to analyze complex problems and develop effective solutions.
  • Familiarity with regulatory requirements and industry standards related to sterile manufacturing.
  • Demonstrated success with talent management and creating an engaged workforce using inclusion as a core principle.

Required Skills:

Accountability Accountability Antibody Drug Conjugates (ADC) Change Agility Collaborative Communications Consulting Continuous Improvement Cross-Cultural Awareness Engineering Design Equipment Maintenance Facility Management GMP Compliance Good Manufacturing Practices (GMP) GxP Compliance Innovation Leadership Leadership Assessments Lean Management Lean Manufacturing Lean Process Improvements Lean Six Sigma Continuous Improvement Maintenance Management Maintenance Strategy Operation Maintenance Operations Management 9 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race color age religion sex sexual orientation gender identity national origin protected veteran status disability status or other applicable legally protected a federal contractor we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences perspectives skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas broad experiences backgrounds and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anothers thinking and approach problems collectively.

Learn more about your rights including under California Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5 2023 employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week Monday - Thursday although the specific days may vary by site or organization with Friday designated as a remote-working day unless business critical tasks require an on-site Hybrid work model does not apply to and daily in-person attendance is required for field-based positions; facility-based manufacturing-based or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note this Hybrid work model guidance also does not apply to roles that have been designated as remote.

The salary range for this role is

$169700.00 - $267200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive if applicable.

We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company 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.

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

10/31/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Director

Job DescriptionWelcome to the Future of Precision Oncology Join Us in Wilmington DE!Were thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington Delawarea bold step forward in transforming cancer care through innovation collaboration an...
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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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