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May 07, 2025

San Diego, CA

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Biomedical Engineering

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":414899,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.183636363636,"Longitude":32.9141818181818,"Distance":null},"State":"California","Zip":"92121","ReferenceID":"SDG-781156","PostedDate":"\/Date(1746645248000)\/","Description":"A global medical technology company in San Diego is looking for a Senior Electrical Engineer to join their team onsite in Sorrento Valley. You will support R\u0026D projects for existing product expansions and technology enhancements of the existing product line. Performs skilled electrical/electronic design duties with the use of applicable hardware tools/equipment under moderate engineering guidance. *Actively participates and provides guidance in the development efforts from concepts to implementation as a project member *Decomposes system requirements into straightforward subsystem and/or electrical specifications and rudimentary designs. *Apply theoretical and hands-on electrical support to identify problems and accomplish tasks *Generates schematic and related files that are ready for PCB layout *Drive PCB layout to the release of a PCBA fabrication package using Allegro Cadence *Develop and execute test documentation for electrical design verification *Understand and follow BD processes, design practices, and documentation templates *Perform and/or direct engineering documentation in SAP: create/change material, BOM, plans, and reports; process change orders; and design reviews *Collaborate with other engineers and departments to advance projects/tasks *Time management of several assignments having varying scope and limited complexity *Provide technical leadership across multiple projects simultaneously *Interface with external design partners and suppliersWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Senior Electrical Engineer","City":"San Diego","ExpirationDate":null,"PriorityOrder":0,"Requirements":". *Bachelor of Science degree in Electrical Engineering or equivalent degree and experience. *At least 4 years of related experience in the medical device field. *Experience with PCB and PCBA circuit design *Knowledge in the use of the laboratory tools: oscilloscope, DMM, variable DC power supply, etc. *Basic wired connectivity and communication with emphasis on LAN, RS485, I2C, and SPI.","Skills":"","Industry":"Biomedical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A global medical technology company in San Diego is looking for a Senior Electrical Engineer to join their team onsite in Sorrento Valley. You will support R&D projects for existing product... expansions and technology enhancements of the existing product line. Performs skilled electrical/electronic design duties with the use of applicable hardware tools/equipment under moderate engineering guidance. *Actively participates and provides guidance in the development efforts from concepts to implementation as a project member *Decomposes system requirements into straightforward subsystem and/or electrical specifications and rudimentary designs. *Apply theoretical and hands-on electrical support to identify problems and accomplish tasks *Generates schematic and related files that are ready for PCB layout *Drive PCB layout to the release of a PCBA fabrication package using Allegro Cadence *Develop and execute test documentation for electrical design verification *Understand and follow BD processes, design practices, and documentation templates *Perform and/or direct engineering documentation in SAP: create/change material, BOM, plans, and reports; process change orders; and design reviews *Collaborate with other engineers and departments to advance projects/tasks *Time management of several assignments having varying scope and limited complexity *Provide technical leadership across multiple projects simultaneously *Interface with external design partners and suppliersWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Apr 30, 2025

Raynham, MA

|

Biomedical Engineering

|

Contract

|

$34 - $42 (hourly estimate)

{"JobID":413734,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.0370818181818,"Longitude":41.9502818181818,"Distance":null},"State":"Massachusetts","Zip":"02767","ReferenceID":"BOS-779309","PostedDate":"\/Date(1746008039000)\/","Description":"Complete validation \u0026 quality actions required for the introduction and delivery of new Hinge cast product line as well as support EUMDR validation assessment and rationalization.The rate for this role varies from $40/HR to $50/HR depending on skillset, experience, and education.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Quality Engineer","City":"Raynham","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Industry: Minimum of 4 years of experience in medical device manufacturing or other highly regulated industries. Understanding of investment casting (foundry processing) is preferred but not required.Validation: Strong background in process validations (IQs, OQ/PQs, TMVs) is required.Quality \u0026 Compliance: Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements). Raises Quality issues as appropriate. Proficiency in conducting non-conformance investigations and maintaining non-conformance records; strong investigation skills and ability to manage multiple investigations are essential. Experience in supporting Corrective and Preventive Actions (CAPA) preferred but not required; includes Action Plan (AP) and Effectivity Monitoring (EM) tasks.Change Control: Experience with change control processing via PLM systems, good documentation practices (tracking edits between revisions), solicit review feedback and approvals.Self-Starter: Demonstrated ability to work independently and proactively. Must be a team player and not shy about engaging with colleagues.Can you describe the purpose of Installation Qualifications (IQs), Operational Qualifications (OQs), Process Qualifications (PQs) and Test Method Validations (TMVs) and what key elements are needed to support those validations?","Skills":"","Industry":"Biomedical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":42.0000,"SalaryLow":33.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Complete validation & quality actions required for the introduction and delivery of new Hinge cast product line as well as support EUMDR validation assessment and rationalization.The rate for this... role varies from $40/HR to $50/HR depending on skillset, experience, and education.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Apr 25, 2025

San Diego, CA

|

Biomedical Engineering

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":413264,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.183363636364,"Longitude":32.9198181818182,"Distance":null},"State":"California","Zip":"92121","ReferenceID":"SDG-778693","PostedDate":"\/Date(1745601240000)\/","Description":"A global medical technology company in San Diego is looking for a Senior Electrical Engineer to join their team onsite in Sorrento Valley. You will support R\u0026D projects for existing product expansions and technology enhancements of the existing product line. Performs skilled electrical/electronic design duties with the use of applicable hardware tools/equipment under moderate engineering guidance.Actively participates and provides guidance in the development efforts from concepts to implementation as a project member Decomposes system requirements into straightforward subsystem and/or electrical specifications and rudimentary designs.Apply theoretical and hands-on electrical support to identify problems and accomplish tasksGenerates schematic and related files that are ready for PCB layoutDrive PCB layout to the release of a PCBA fabrication package using Allegro CadenceDevelop and execute test documentation for electrical design verificationUnderstand and follow BD processes, design practices, and documentation templatesPerform and/or direct engineering documentation in SAP: create/change material, BOM, plans, and reports; process change orders; and design reviewsCollaborate with other engineers and departments to advance projects/tasksTime management of several assignments having varying scope and limited complexityProvide technical leadership across multiple projects simultaneouslyInterface with external design partners and suppliersWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Senior Electrical Engineer","City":"San Diego","ExpirationDate":null,"PriorityOrder":0,"Requirements":".Bachelor of Science degree in Electrical Engineering or equivalent degree and experience.At least 4 years of related experience in the medical device field.Experience with PCB and PCBA circuit designKnowledge in the use of the laboratory tools: oscilloscope, DMM, variable DC power supply, etc.Basic wired connectivity and communication with emphasis on LAN, RS485, I2C, and SPI.","Skills":"","Industry":"Biomedical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A global medical technology company in San Diego is looking for a Senior Electrical Engineer to join their team onsite in Sorrento Valley. You will support R&D projects for existing product... expansions and technology enhancements of the existing product line. Performs skilled electrical/electronic design duties with the use of applicable hardware tools/equipment under moderate engineering guidance.Actively participates and provides guidance in the development efforts from concepts to implementation as a project member Decomposes system requirements into straightforward subsystem and/or electrical specifications and rudimentary designs.Apply theoretical and hands-on electrical support to identify problems and accomplish tasksGenerates schematic and related files that are ready for PCB layoutDrive PCB layout to the release of a PCBA fabrication package using Allegro CadenceDevelop and execute test documentation for electrical design verificationUnderstand and follow BD processes, design practices, and documentation templatesPerform and/or direct engineering documentation in SAP: create/change material, BOM, plans, and reports; process change orders; and design reviewsCollaborate with other engineers and departments to advance projects/tasksTime management of several assignments having varying scope and limited complexityProvide technical leadership across multiple projects simultaneouslyInterface with external design partners and suppliersWe are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 08, 2025

Spokane, WA

|

Engineering (Non IT)

|

Contract

|

$44 - $55 (hourly estimate)

{"JobID":415046,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.539090909091,"Longitude":47.6444545454546,"Distance":null},"State":"Washington","Zip":"99224","ReferenceID":"PHL-781374","PostedDate":"\/Date(1746713651000)\/","Description":"One of our large pharmaceutical clients is actively hiring for a Technical Transfer Project Engineer, specializing in sterile filling, supporting the external manufacturing team. This person will be supporting tech transfers for vaccine and biologic drug products and traveling 3 weeks per month onsite at the CMO on the west coast. The client is executing sterile drug product technical transfers and would need a Project/Process Engineer to support the program by authoring technical documentation and supporting technical development studies through protocol development, floor execution, sample submission, data analysis, and reporting. As needed, support may be required for routine commercial drug product production (change controls, data analysis, etc.). This candidate will take process designs, author protocols, and execute different studies at commercial scale. These studies may include but are not limited to mixing studies, fill line studies, engineering batches, etc. You will be hands on with manufacturing of filled vials or syringes and submitting product samples to labs for analysis. The Engineer will also help with data analysis and author reports based off their findings. The client currently uses Microsoft Office-based software and statistical analysis programs (JMP). You will be integrated into the project teams and involved in the transfer of sterile drug products for commercialization - such as manufacturing drugs at a larger scale, stability testing, drug development, and transfer into their final primary containers, such as vials or syringes, under controlled aseptic conditions. This role is 75% travel so ideally looking for local candidates.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Technical Transfer Project Engineer","City":"Spokane","ExpirationDate":null,"PriorityOrder":0,"Requirements":"3-4 years\u0027 experience in pharmaceutical manufacturing B.A./B.S in Mechanical Engineering, Biomedical Engineering, Industrial and System Engineering or other types of engineering.Involvement in sterile drug product technical transfers Experience in Sterile Manufacturing, STRONG preference in sterile filling (also called Aseptic)Technical Writing \u0026 Change Control","Skills":"","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":55.0000,"SalaryLow":44.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large pharmaceutical clients is actively hiring for a Technical Transfer Project Engineer, specializing in sterile filling, supporting the external manufacturing team. This person will be... supporting tech transfers for vaccine and biologic drug products and traveling 3 weeks per month onsite at the CMO on the west coast. The client is executing sterile drug product technical transfers and would need a Project/Process Engineer to support the program by authoring technical documentation and supporting technical development studies through protocol development, floor execution, sample submission, data analysis, and reporting. As needed, support may be required for routine commercial drug product production (change controls, data analysis, etc.). This candidate will take process designs, author protocols, and execute different studies at commercial scale. These studies may include but are not limited to mixing studies, fill line studies, engineering batches, etc. You will be hands on with manufacturing of filled vials or syringes and submitting product samples to labs for analysis. The Engineer will also help with data analysis and author reports based off their findings. The client currently uses Microsoft Office-based software and statistical analysis programs (JMP). You will be integrated into the project teams and involved in the transfer of sterile drug products for commercialization - such as manufacturing drugs at a larger scale, stability testing, drug development, and transfer into their final primary containers, such as vials or syringes, under controlled aseptic conditions. This role is 75% travel so ideally looking for local candidates.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 01, 2025

Collegeville, PA

|

Chemical Engineering

|

Contract

|

$38 - $47 (hourly estimate)

{"JobID":414041,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.4292727272727,"Longitude":40.1813636363636,"Distance":null},"State":"Pennsylvania","Zip":"19426","ReferenceID":"PHL-779741","PostedDate":"\/Date(1746119645000)\/","Description":"One of our large Pharmaceutical clients is actively hiring for a Process Engineer to join the R\u0026D biopharma and small molecules Drug Product Development Team. This team supports sterile products and mostly new product introduction. The main products they will be supporting are suspension products. Responsibilities include:? Work as a Process Engineer in a multi-disciplinary development team, liaising efficiently with Formulators, Modelers, automation experts, data scientists and device engineers, to deliver the work packages required to understand drug product unit operations and scale these-up effectively.? Work on developing processes for lyophilized drug product dosage forms and other Steriles process development. ? Support continuous improvements in the drug product development process through technological innovation and application of first principles in lyophilization process engineering? Actively participate in technical reviews on projects, lead the technical transfer of processes, and ensure timely execution, while collaborating actively with R\u0026D Pilot Plants and Global Supply Chain manufacturing sites. This is a hybrid position and a continuous project.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Process Engineer","City":"Collegeville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelors / Masters, or PHD in Chemical Engineering or Biomedical Engineering3-5 years\u0027 experience in Drug Product Manufacturing Sterile / Suspension Product experienceExperience in Freeze Drying/Lyophilization requiredData Modeling / Python Programming preferred (process simulation, digital twin, chemometrics)","Skills":"Experience in Steriles drug product process development, PAT, characterization, scale -up and technology transfer, modelling, to deliver processes -Experience in the application of state-of-the-art laboratory equipment, equipment automation, data automation, PAT tools and modelling software.-Experience evaluating, developing, and qualifying manufacturing equipment.","Industry":"Chemical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":47.0000,"SalaryLow":37.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large Pharmaceutical clients is actively hiring for a Process Engineer to join the R&D biopharma and small molecules Drug Product Development Team. This team supports sterile products and... mostly new product introduction. The main products they will be supporting are suspension products. Responsibilities include:? Work as a Process Engineer in a multi-disciplinary development team, liaising efficiently with Formulators, Modelers, automation experts, data scientists and device engineers, to deliver the work packages required to understand drug product unit operations and scale these-up effectively.? Work on developing processes for lyophilized drug product dosage forms and other Steriles process development. ? Support continuous improvements in the drug product development process through technological innovation and application of first principles in lyophilization process engineering? Actively participate in technical reviews on projects, lead the technical transfer of processes, and ensure timely execution, while collaborating actively with R&D Pilot Plants and Global Supply Chain manufacturing sites. This is a hybrid position and a continuous project.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

May 06, 2025

West Point, PA

|

Engineering (Non IT)

|

Contract

|

$32 - $40 (hourly estimate)

{"JobID":414599,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.2747272727273,"Longitude":40.2212727272727,"Distance":null},"State":"Pennsylvania","Zip":"19486","ReferenceID":"PHL-780694","PostedDate":"\/Date(1746548057000)\/","Description":"One of our large pharmaceutical clients is actively hiring a packaging commercialization engineer for their team. This person will be supporting the design testing and distribution qualification for critical upcoming projects. The ideal candidate will have a strong background in packaging development, particularly for traditional pharmaceuticals, and a passion for creating innovative packaging solutions that meet regulatory standards and support commercialization efforts.Responsibilities include:-Focus on package development for the delivery of traditional pharmaceuticals, including oral solid dosage forms and sterile products, as well as supporting combination product development projects.-Provide input regarding the selection of primary and secondary packaging materials, ensuring optimal performance and compliance with industry standards.-Determine package images that support commercialization efforts and lead the execution of distribution qualification testing to assess the robustness of packaging solutions.-Author comprehensive packaging specifications for primary, secondary, and tertiary packaging, ensuring all documentation meets regulatory requirements.-Provide necessary information to support relevant sections of New Drug Applications (NDA), Worldwide Marketing Applications (WMA), and Japanese New Drug Applications (JNDA).-Interface effectively with packaging component suppliers, Global Packaging Technology Operations, Packaging Site Operations, and Contract Manufacturing Operations to fulfill packaging responsibilities.This is a hybrid role for a 6 month contract, potential extensions.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Packaging Engineer","City":"West Point","ExpirationDate":null,"PriorityOrder":0,"Requirements":"B.S. or higher degree in Biomedical Engineering, Chemical Engineering, Materials Science, Packaging Engineering, Packaging Science, or Pharmaceutical Science.A minimum of 2 years of relevant experience in packaging development, with a strong emphasis on package developmentProven ability to author protocols and execute studies, demonstrating strong technical writing skills.","Skills":"","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":40.0000,"SalaryLow":32.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large pharmaceutical clients is actively hiring a packaging commercialization engineer for their team. This person will be supporting the design testing and distribution qualification for... critical upcoming projects. The ideal candidate will have a strong background in packaging development, particularly for traditional pharmaceuticals, and a passion for creating innovative packaging solutions that meet regulatory standards and support commercialization efforts.Responsibilities include:-Focus on package development for the delivery of traditional pharmaceuticals, including oral solid dosage forms and sterile products, as well as supporting combination product development projects.-Provide input regarding the selection of primary and secondary packaging materials, ensuring optimal performance and compliance with industry standards.-Determine package images that support commercialization efforts and lead the execution of distribution qualification testing to assess the robustness of packaging solutions.-Author comprehensive packaging specifications for primary, secondary, and tertiary packaging, ensuring all documentation meets regulatory requirements.-Provide necessary information to support relevant sections of New Drug Applications (NDA), Worldwide Marketing Applications (WMA), and Japanese New Drug Applications (JNDA).-Interface effectively with packaging component suppliers, Global Packaging Technology Operations, Packaging Site Operations, and Contract Manufacturing Operations to fulfill packaging responsibilities.This is a hybrid role for a 6 month contract, potential extensions.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

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