3key Consulting, Inc.
Senior Engineer, Biotech Manufacturing/Packaging Lines (JP14376)
3key Consulting, Inc., New Albany, Ohio, United States, 43054
Job Title:
Senior Engineer, Biotech Manufacturing/Packaging Lines (JP14376) Location: New Albany, OH. 43054 Employment Type: Contract Business Unit: Manufacturing Systems Engineering Duration: 1+ years with likely extensions and/or conversion to permanent Posting Date: 08/07/2025 Pay Rate: $40 - $46/hour W2 with benefits
3 Key Consulting is hiring a Senior Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Ideal Candidate:
4+ YOE, experience supporting a manufacturing line, and GMP or regulated environment experience. Nice to have:
relevant pharma experience, experience starting up a new manufacturing line.
Job Description: In this role the Senior Engineer (Line Owner/System Owner) must work under general supervision, owns all the technical aspects in a manufacturing line. The processes 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 design requirements to the service providers to fulfill area technical and equipment needs.
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.
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 Contex
Why is the Position Open? Supplement additional workload on team
Top Must Have Skills:
Experience in a manufacturing environment, preferably GMP regulated or other highly regulated environment Experience working hands-on to solve technical problems on manufacturing equipment Great communication skills
Day to Day Responsibilities:
Act as the equipment technical subject matter expert for an end-to-end pharmaceutical device assembly and packaging line. This individual is responsible for working with the maintenance and automation teams to resolve complex issues that are escalated beyond the technician level. This individual also leads improvement projects to increase line OEE.
Basic Qualifications: Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience.
Employee Value Proposition:
Leading Biotech Experience
Red Flags: Any time at companies shorter than 6mo, although the hiring team understands some contracts are shorter.
Interview process: Round 1 - 1 on 1 interview with hiring manager Round 2 - Panel interview with 2-3 engineers/managers
We invite qualified candidates to sendyour resume to resumes@3keyconsulting.com . Ifyou decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
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Senior Engineer, Biotech Manufacturing/Packaging Lines (JP14376) Location: New Albany, OH. 43054 Employment Type: Contract Business Unit: Manufacturing Systems Engineering Duration: 1+ years with likely extensions and/or conversion to permanent Posting Date: 08/07/2025 Pay Rate: $40 - $46/hour W2 with benefits
3 Key Consulting is hiring a Senior Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Ideal Candidate:
4+ YOE, experience supporting a manufacturing line, and GMP or regulated environment experience. Nice to have:
relevant pharma experience, experience starting up a new manufacturing line.
Job Description: In this role the Senior Engineer (Line Owner/System Owner) must work under general supervision, owns all the technical aspects in a manufacturing line. The processes 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 design requirements to the service providers to fulfill area technical and equipment needs.
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.
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 Contex
Why is the Position Open? Supplement additional workload on team
Top Must Have Skills:
Experience in a manufacturing environment, preferably GMP regulated or other highly regulated environment Experience working hands-on to solve technical problems on manufacturing equipment Great communication skills
Day to Day Responsibilities:
Act as the equipment technical subject matter expert for an end-to-end pharmaceutical device assembly and packaging line. This individual is responsible for working with the maintenance and automation teams to resolve complex issues that are escalated beyond the technician level. This individual also leads improvement projects to increase line OEE.
Basic Qualifications: Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience.
Employee Value Proposition:
Leading Biotech Experience
Red Flags: Any time at companies shorter than 6mo, although the hiring team understands some contracts are shorter.
Interview process: Round 1 - 1 on 1 interview with hiring manager Round 2 - Panel interview with 2-3 engineers/managers
We invite qualified candidates to sendyour resume to resumes@3keyconsulting.com . Ifyou decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
#J-18808-Ljbffr