Job DescriptionPosition SummaryThe Technical Project Manager (TPM) is responsible for delivering digital, automation, and data integration scope across capital projects within the Digital Manufacturing Division Manufacturing Value Team portfolio. This role ensures the reliable, compliant, and scalable implementation of process automation and manufacturing digital systems that support facility startup, operational readiness, and sustained manufacturing performance.
The TPM leads defined project scopes or workstreams across the full project lifecycle, embedding automation architecture, data integrity, cybersecurity, and validation requirements into project execution. This role works closely with Engineering, Automation, IT, Quality, Manufacturing Operations, and external partners to deliver robust, compliant solutions aligned with cGMP, data integrity, and lifecycle management best practices.
Key Responsibilities and Expectations- Lead end-to-end delivery of digital and automation scope across capital project phases, including FEL, detailed design, construction, commissioning, and qualification
- Manage scope, schedule, cost, risks, and dependencies to ensure alignment with project objectives and milestones
- Monitor project performance and proactively identify and resolve issues impacting delivery
- Deliver process automation, MES, and data integration solutions, including DCS, PLC-based platforms, historians, and reporting/analytics tools
- Support development of user requirements, functional/design specifications, and validation deliverables
- Ensure technical solutions meet quality, data integrity, cybersecurity, and lifecycle management requirements
- Coordinate system integration across automation platforms, OEM equipment, and enterprise data systems
- Support FAT/SAT, installation, commissioning, and qualification of automation systems
- Partner with Engineering, Automation, IT, Quality, Operations, vendors, and system integrators to support aligned execution
- Support stage-gate governance, project reviews, and accurate status reporting to stakeholders and leadership
- Ensure systems are delivered in a validated, compliant state and support readiness for startup and transition to operations
- Operate within established governance frameworks while independently driving day-to-day execution
- Escalate complex risks, cross-project impacts, and constraints as needed
- Apply technical judgment, structured problem-solving, and root cause analysis to resolve issues
Success Measures- Successful delivery of digital and automation scope aligned with project schedule, budget, and quality expectations
- Effective integration and performance of automation and manufacturing systems
- Clear and proactive communication of project status, risks, and issues
- Contribution to successful facility startup, validation, and operational readiness
Required Qualifications- Bachelor's degree in Engineering, Computer Science, or a related technical discipline, plus a minimum of 5 years of relevant technical support or manufacturing automation experience, or equivalent related experience
- Experience supporting delivery of automation or digital scope within pharmaceutical, biotech, or regulated manufacturing environments
- Working knowledge of automation systems (DeltaV, PLC/SCADA) and manufacturing digital platforms (MES, historians, data integration)
- Demonstrated ability to manage project scope, schedule, deliverables, and cross-functional coordination
Preferred Qualifications- Experience supporting capital projects across lifecycle phases, from FEL through commissioning and qualification
- Familiarity with cGMP, validation, data integrity, and quality systems for computerized systems
- Experience supporting system integration, commissioning, and qualification of automated equipment
- Experience working with vendors, system integrators, and global cross-functional teams
- Programming experience with Ladder Logic, Sequential Function Charts, Python, and/or other scripting languages for automation, testing, and reporting
- Knowledge of S88 batch standards
- Experience in biologics, vaccine, or bulk sterile manufacturing facilities strongly preferred
- OT/IT experience, including industrial networking, virtualization (e.g., VMs), databases/historians, and basic system administration
- Experience with electronic validation and quality systems (e.g., Kneat/eVal, Veeva)
Required Skills: Measurement Analysis, Portfolio, Programme, and Project Support, Program Management, Risk Management, Stakeholder Relationship Management, Waterfall Model
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.
The salary range for this role is
$117,000.00 - $184,200.00
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:25%
Flexible Work Arrangements:Hybrid
Shift:Not Indicated
Valid Driving License:No
Hazardous Material(s):n/a
Job Posting End Date:07/1/2026
*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. 
