Senior Specialist, Operations - (Drug Product)

Merck & Co.

Elkton (VA)

On-site

USD 96,000 - 151,000

Full time

14 days+

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Benefits offered by this job

Annual bonus

Long-term incentive

401(k)

Job summary

Merck & Co., Inc. is building a new Small Molecule manufacturing site in Elkton, VA, and seeks a DP Operations Specialist to support commissioning, qualification, start-up, and ongoing operations.

You will partner with Operations, Engineering, Quality, and Technical teams to ensure safe, compliant, and efficient start-up and production as the site scales. With 5+ years in Drug Product/SDI manufacturing and a strong background in GMP, you will help drive continuous improvement and lean practices,

Qualifications

Bachelor's degree in Chemical Engineering, Pharmaceutical Engineering, Biochemical Engineering, Chemistry, or related technical discipline.
Minimum 5 years of experience in Drug Product/SDI manufacturing, including operations.
Experience in cross-functional manufacturing/technical environments with process support or start-up activities.
Knowledge of GMP, quality and compliance in pharma manufacturing.
Strong problem-solving, communication, collaboration, and organization skills.

Responsibilities

Support commissioning, qualification, start-up, and readiness for the new Small Molecule facility in Elkton, VA.
Collaborate with Operations, Engineering, Quality, Technical Operations, and Supply Chain for safe, compliant plant start-up.
Provide technical and operational support during start-up, troubleshooting, and optimization.
Assist technology transfer and implementation of commercial processes in the new facility.
Define and improve operating practices, standard work, and procedures for reliable operations.

Skills

Adaptability

Analytical Problem Solving

Biopharmaceutical Industry

cGMP Compliance

Data Analysis

Decision Making

Inventory Management

Lean Management

Operational Excellence

Process Optimization

Education

Bachelor's degree in Chemical Engineering or related technical discipline

Job description

Job Description

At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.

Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence.

At our site, you'll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best work. We are building deep small molecule expertise in the U.S., and we want team members who are excited to grow their skills, help improve how we operate, and contribute to a site positioned for future growth.

Reports To:

Production Lead, DP&SDI

Job Purpose:

The-DP (Drug Product) Operations Specialist-supports the DP and SDI Integrated Product Team (IPT) in the commissioning, qualification, start-up, and operational readiness of the new Small Molecule manufacturing facility in Elkton, Virginia. This role partners with cross‑functional teams to help ensure safe, compliant, and efficient operations during project execution and through ongoing manufacturing. In addition, the DP Operations Engineer helps coordinate and prioritize improvement activities and areas of focus across the IPT, supporting continuous improvement and operational excellence as the facility transitions into routine operations.

Primary Responsibilities:

Support commissioning, qualification, start-up, and operational readiness activities for the new DP Small Molecule facility in Elkton, VA.
Partner with Operations, Engineering, Quality, Technical Operations, Supply Chain, and other stakeholders to support safe, compliant, and effective plant start‑up.
Provide technical and operational support during equipment and process start‑up, troubleshooting, and optimization activities.
Support technology transfer and implementation of commercial manufacturing processes into the new facility.
Help define, implement, and improve operating practices, standard work, procedures, and routines that support reliable and compliant operations.
Coordinate and prioritize improvement activities and key areas of focus within the IPT in alignment with business objectives and operational performance goals.
Use our company Production System (MPS) tools and lean principles, including Kaizen, 5S, visual management, and Standard Work, to identify and support improvement opportunities.
Help embed best practices across shifts, functions, and workstreams to promote consistency, efficiency, and strong operational execution.
Support a culture of safety, quality, compliance, accountability, and continuous improvement.
Act as a delegate for the Production Lead when needed, supporting continuity of leadership and cross‑functional coordination.
Contribute to an inclusive, collaborative, and performance‑driven work environment.

Minimum Required Education, Experience:

Bachelor's degree. Chemical Engineering, Pharmaceutical Engineering, Biochemical Engineering, Chemistry, or a related technical discipline. Engineering degree not required.
Minimum 5 years of experience in Drug Product/SDI manufacturing, to include operations, technical operations
Experience working in a cross‑functional manufacturing, technical, or operational setting.
Experience contributing to operational improvement, troubleshooting, process support, or start‑up‑related activities.
Working knowledge of GMP, quality, and compliance expectations in pharmaceutical manufacturing.
Strong problem‑solving, communication, collaboration, and organizational skills.
Ability to work effectively across Operations, Engineering, Quality, and Technical teams.
Ability to prioritize work in a dynamic, fast‑paced environment.
Demonstrated commitment to safety, operational excellence, and continuous improvement.

Preferred Qualifications:

Experience supporting commissioning, qualification, start‑up, or validation activities.
Experience in a greenfield or new facility start‑up environment.
Experience with technology transfer and implementation of commercial manufacturing processes.
Experience applying lean tools and methodologies, including Kaizen, 5S, and Standard Work.
Experience coordinating activities across shifts, teams, or functions.
Experience serving in a lead, coordinator, or delegate role supporting leadership continuity.
Experience identifying improvement opportunities and helping implement practical solutions in a manufacturing environment.

Required Skills:

Adaptability, Adaptability, Analytical Problem Solving, Biopharmaceutical Industry, cGMP Compliance, Data Analysis, Decision Making, GMP Compliance, Inventory Management, Lean Management, Lean Process Improvements, Lean Six Sigma Continuous Improvement, Manufacturing Environments, Manufacturing Operations, Manufacturing Technologies, Operational Excellence, Personal Initiative, Pharmaceutical Manufacturing, Pharmaceutical Process Engineering, Process Improvements, Process Optimization, Production Planning, Production Scheduling, Technical Acumen, Technology Transfer {+ 2 more}

This is a unique opportunity to help shape the future of a growing Small Molecule site as it is established from the ground up. In this role, you will support the startup and operational readiness of the new facility, help establish effective ways of working, and contribute to continuous improvement efforts that enable safe, reliable, and high‑quality medicine production for patients around the world. If you are a collaborative operations professional with strong technical acumen, a commitment to quality, and a passion for operational excellence, we encourage you to apply.

#ELKVACOE

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: 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 another's thinking and approach problems collectively.

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

The salary range for this role is $96,200.00 - $151,400.00

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.

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.

Additional Details: