Engineer, Biotech Packaging Line Equipment (JP13921)
Company: 3 Key Consulting
Location: New Albany
Posted on: April 1, 2026
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Job Description:
Job Title: Engineer, Biotech Packaging Line Equipment (JP13921)
Location: New Albany, OH. 43054 Business Unit: Assembly & Packaging
Chimera Employment Type: Contract Duration: Initial 6 months with
likely extensions or conversion to FTE Rate : $40-50/Hr or open
market rate DOE, W2 with Benefits Posting Date: 4/3/2025. Note :
seeking 3 years of experience 3 Key Consulting is hiring! We are
recruiting Engineer (Mechanical) - Biotech Packaging Lines
Equipment for a consulting engagement with our direct client, a
leading global biotechnology company. Job Description: In this role
the Line Owner/System Owner must work under general supervision,
owning all the technical aspects in a manufacturing line. The
processes where the SO/LO Engineer shall be familiar with are:
Characterization of process optimization strategies and/or solving
problems of operational issues in the packaging operations,
manufacturing, pilot technologies or capital projects. Apply basic
engineering principles to the design and implementation of system
modifications, experiments and/or capital projects. Organizes,
analyzes and presents interpretation of results for operational
issues or engineering projects of minor scope and complexity. As a
technical resource of an area, System owner / Line Owner Engineer
shall interact and provide direction to technical resources such as
Mechanics, Automation Techs and IS teams. At the same time, the
System Owner/Line Owner Engineer shall be able to define designs
requirement to the service providers to fulfill area technical and
equipment needs. Top Must Have Skill Sets: Experience with
packaging equipment, specifically pharmaceutical, food, or
beverage. Experience with GMP environments. Good communication
skills, troubleshooting skills, and a team player. Looking for
Mechanical engineer over an industrial engineer (industrial is OK
with relevant experience) Day to Day Responsibilities: Specific
responsibilities include but are not limited to: Provide solutions
to a variety of technical problems of moderate scope and
complexity. Under general supervision will evaluate, select and
apply standard engineering techniques and procedures. Assistance
given for unusual problems. Perform assignments that have clear and
specific objectives and require investigation of limited number of
variables. Initiate and complete routine technical tasks.
Operations Engineering: Function as a technical specialist to
equipment or systems regarding problem solving operations.
Frequently become actively involved in daily operations when
required to meet schedules or to resolve problems. Routinely audit
the operational performance and regulatory compliance of a moderate
number of equipment items or systems of complexity. Work with
research, manufacturing, maintenance, process development,
utilities, facilities, quality assurance and/or validation
departments in developing requirements and recommendations for
system modifications. Design Engineering: Work under the direct
supervision of project managers to complete design, engineering,
and construction projects within schedule and budget constraints.
Work with consultants, architects and engineering firms on
development of standard design documents. Acquire and critique
quotes for equipment modifications or installations. Generate
rudimentary project cost estimates and schedules. Basic
Qualifications: Master degree OR Bachelor degree and 2 years of
experience OR Associate degree and 6 years of experience OR High
school diploma / GED and 8 years of experience Preferred
Qualifications: Advanced degree in Mechatronics, Computer,
Electrical, Mechanical, or Chemical Engineering Knowledge and/or
experience of pharmaceutical/biotech processes, especially in the
area of final drug product operations Knowledge of
pharmaceutical/biotech processes Familiarity with validation
processes for Packaging areas Familiarity with serialization
process and networking Familiarity with documentation in a highly
regulated environment Ability to operate specialized equipment,
tools and computers as appropriate. Ability to interpret and apply
GAMPs and GMPs and familiarity with documentation in a highly
regulated environment. Ability to apply engineering science to
production. Able to develop solutions to routine technical problems
of limited scope Comprehensive understanding of protocol
requirements. Organizational, project management, problem-solving,
as well as validation protocol, and technical writing capability
Excellent communication (verbal/written) and presentation skills
Demonstrated interpersonal skills including; collaboration,
influencing, and facilitation Protocol and script testing Writing
Dealing with and handling change Packaging Equipment Technical
knowledge Analytical Problem Solving Comprehensive understanding of
validation protocol implementation requirements as well as
knowledge of validation processes and requirements as applied to
new equipment installations Understanding of Operational Excellence
and Lean Transformation in the Automation and Engineering Context
Why is the Position Open? Supplement additional workload on team.
Red Flags: Misspellings in Resume. Long Resumes without descriptive
content. Interview Process: One phone and one virtual panel
interview. We invite qualified candidates to send your resume to
recruiting@3keyconsulting.com . If you decide that you’re not
interested in pursuing this particular position, please feel free
to take a look at the other positions on our website
www.3keyconsulting.com/careers. You are also welcome to share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Newark , Engineer, Biotech Packaging Line Equipment (JP13921), Engineering , New Albany, Ohio
