×
Register Here to Apply for Jobs or Post Jobs. X

Specialist, Engineering

Job in Wilson, Wilson County, North Carolina, 27893, USA
Listing for: Merck
Full Time position
Listed on 2026-01-01
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering
Job Description & How to Apply Below

Join to apply for the Specialist, Engineering role at Merck.

Our engineers and scientists support internal and external manufacturing operations to remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our technical personnel have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

Summary, Focus And Purpose

The Vaccines Technology Specialist position is responsible for providing technical support to primary filling, inspection, and/or packaging operations within the vaccine manufacturing facility at the Wilson, NC Site. This position will be an individual contributor and member of the Technical Operations Team within the Rota-POD Integrated Process Team.

This is an engineering role focused on the technical & commercial readiness of the vaccine manufacturing facility as well as providing future routine operational support. For their area of assignment, the selected candidate will be the technical subject matter expert for all aspects of tech transfer, validation, licensure, start up, and ongoing technical support.

Key Functions Delivery
  • Utilize technical expertise, experience, independent judgment, and decision-making to build robust processes that support consistent and reliable supply
  • Resolve and elevate technical issues impacting supply within the daily, weekly, and monthly IPT management processes
  • Lead or support equipment process development, troubleshooting and validation activities
Compliance
  • Ensure that assigned processes are developed in a robust manner and defined such that vaccines filled at the Wilson site consistently meet critical quality attributes
  • Act as or support technical subject matter expert(s) during regulatory inspections for area of assignment
  • Ensure that process development and validation data is generated, documented and presented in a manner that supports successful licensure and positive interactions with regulatory agencies
  • Lead or support change management for the Rota-POD IPT and provide scientific/technical justification for proposed changes to support business needs
  • Investigate, determine root cause, and implement robust Corrective Action and Preventive Actions and author quality investigations for any applicable process related compliance discrepancies noted during day-to-day activities and/or audits, and raise these issues per IPT management processes
Cost
  • Ensure that technical related activities for area of assignment are managed such that process deliverables and timelines are well defined in advance and met
  • Recommend continuous improvement, productivity, and capital projects for the IPT
Continuous Improvement
  • Execute projects that support the strategic goals of the Rota-POD IPT
  • Maintain a culture of continuous improvement focused on standard work, making problems visible, minimizing waste, reducing process variability, and problem solving
Education
  • Bachelor's degree or higher in Science or Engineering field (Engineering preferred)
Required Experience | Knowledge | Skills
  • Two years of relevant industry work experience, with one year experience providing technical/development support to pharmaceutical unit operations
  • Working knowledge of cGMPs and of regulatory requirements as they apply to the vaccine/pharmaceutical industry
  • Technical writing experience with investigations, change requests, standard operating procedures, batch records, protocols, etc.
  • Demonstrated ability to work independently as team member
  • Demonstrated strong interpersonal skills with ability to influence and support others through a culture of inclusion, feedback, and empowerment
  • Willing to work irregular hours to support multi-shift operation on an extended or as needed basis
Preferred Experience | Knowledge | Skill
  • Experience with aseptic filling, qualified inspection processes, pharmaceutical packaging and/or serialization/aggregation
  • Experience in production ramp up of capital projects
  • Experience in authoring quality deviations
  • Experience in Continuous Improvement, Lean Manufacturing, Problem Solving, and/or Right…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary