Engineer, Biotech Manufacturing Line (JP12155)
Company: 3 Key Consulting
Location: New Albany
Posted on: April 1, 2026
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Job Description:
Job Title: Engineer, Biotech Manufacturing Line (JP12155)
Location: New Albany, OH. 43054 Business Unit: Assembly & Packaging
Employment Type: Contract Duration: 1 years (with possible
extensions) Rate : $35 - $37/hour Posting Date: 1/10/2024. Notes:
Only qualified candidates need apply. Fully onsite in New Albany
OH. 43054 3 Key Consulting is hiring! We are recruiting an Engineer
Biotech Manufacturing Line 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. Applies 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
resumes@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, Elyria , Engineer, Biotech Manufacturing Line (JP12155), Engineering , New Albany, Ohio
