Job Description

At our Wilmington Biotech Campus, we are committed to keeping the patient at the very heart of all that we do and striving to find solutions and treatments for some of the world’s most challenging healthcare needs.

The Wilmington Biotech Campus will play a pivotal role in the manufacture of our company’s biologics-based medicines, including the areas of immuno-oncology. This site will establish our company’s internal capability to manufacture high potent compounds when full manufacturing operations begin in 2029.

This facility will be a significant supplier of Antibody Drug Conjugates (ADCs) and High Potent Compounds and will also be critical in the future supply of new biotechnology products to its global network.

Wilmington Biotech Campus – Quality Control Laboratory

The Quality Control (QC) Laboratory at Wilmington Biotech Campus will be a transformational facility for the analytical commercialization of our company’s pipeline of high potent Biologics. This laboratory will bring together late-stage analytical method development and validation with commercial release testing to deliver significantly improved speed through the analytical lifecycle. The laboratory will be supported by locally based advanced analytical subject matter experts and digital tools to enable an enterprise-wide connected laboratory in support of a new approach to analytical commercialization for high potent Biologics. The laboratory will be operated under our Manufacturing Division with close collaboration with our Research & Development Division.

Reporting to the QC lead for Instrumentation & Digital Systems, the Quality Control Instrument Specialist will support the start-up and ongoing operation of new laboratory facilities by assisting with the procurement, commissioning, qualification, and lifecycle management of analytical instrumentation. This role ensures that laboratory instruments are maintained in a validated and calibrated state to support analytical testing in compliance with regulatory and quality standards.

Key Accountabilities:

New Facility & Laboratory Start-Up:

• Support the procurement and installation of laboratory instrumentation, including coordination with vendors and internal stakeholders

• Assist with the development and execution of instrument commissioning and qualification (IQ/OQ/PQ) protocols

• Prepare and review supporting documentation for instrument qualification activities to ensure the highest standards of execution including SOPs, maintenance plans, equipment classifications, and qualification documentation

• Coordinate with Quality Assurance (QA), Information Technology (IT), and Global Engineering Services (GES) functions to ensure commissioning and qualification activities are completed on schedule to support operational readiness

• Support interaction with qualification services providers and external laboratory support groups

Post Go-Live Instrument Lifecycle Management:

• Execute maintenance and calibration activities in accordance with established schedules and regulatory expectations

• Ensure all laboratory instrumentation is maintained in a fully validated and calibrated state in support of analytical testing

• Support the instrument management quality system, including documentation of instrument status, deviations, and change controls

• Assist with troubleshooting instrument issues and coordinating repairs with vendors

• Maintain inspection readiness of all laboratory instruments and systems at all times

Quality & Compliance:

• Support the development and maintenance of instrument-related SOPs, work instructions, and quality system documentation in compliance with cGMP, biosafety, corporate policies, and regulatory requirements

• Ensure compliance with Data Integrity and Good Documentation Practices requirements related to laboratory instrumentation

• Support and/or lead equipment troubleshooting and related deviations, CAPAs, and change controls

• Participate in internal audits and support health authority inspections as needed

Collaboration & Development:

• Liaise with cross-functional teams including our research division, IT, Quality Assurance, and Engineering

• Support training activities for laboratory personnel on instrument operation and maintenance

• Contribute to continuous improvement initiatives for instrumentation processes

Qualifications / experience

Education

• Bachelor's degree in Chemistry, Biochemistry, Engineering, or a related scientific discipline.

Experience

• Minimum 2 years of industry experience in a regulated laboratory environment (pharmaceutical, biotech, or related industry)

• Experience with analytical instrumentation commonly used in QC laboratories (e.g., HPLC/UPLC, plate readers, mass spectrometers, analytical balances, etc.)

• Familiarity with instrument qualification (IQ/OQ/PQ) and calibration principles

• Exposure to GMP environments and quality management systems is required

• Experience with core laboratory & quality systems including Empower, Softmax Pro, GLIMS, LabX, MODA, Biovia, SAP, Veeva, etc.

Core competencies and skills

• Strong attention to detail and documentation practices

• Strong critical thinking skills and troubleshooting capabilities

• Good organizational and time management skills

• Ability to work collaboratively in a team environment

• Basic understanding of Data Integrity principles

• Familiarity with laboratory IT systems and electronic data management

• Effective written and verbal communication skills

Additional Info:

• Location: Wilmington Delaware (On-Site)

• Travel: Ability to travel ~10% of the time

Required Skills:

Analytical Instrumentation, Analytical Testing, Antibody Drug Conjugates (ADC), Critical Thinking, Data Integrity, Driving Continuous Improvement, GMP Compliance, Laboratory Documentation, Laboratory Safety, Mass Spectrometry (MS), Quality Control Documentation, Quality Systems Documentation, Regulatory Requirements, Teamwork, Technical Writing, Troubleshooting, Use of Laboratory Equipment

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 characteristics. As 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:

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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 another’s thinking and approach problems collectively.

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The salary range for this role is

$87,300.00 - $137,400.00

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 employee’s 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 https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

Yes

Job Posting End Date:

07/28/2026

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