Operations Engineer; Product Transfer & Manufacturing Suppor Mawah, NJ _ ONSITE
Job in
Mahwah, Bergen County, New Jersey, 07430, USA
Listed on 2026-06-14
Listing for:
Matlen Silver, Inc.
Full Time
position Listed on 2026-06-14
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer, Validation Engineer -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Description
Operations Engineer (Product Transfer & Manufacturing Suppor)
Mahwah, NJ (Onsite)
12-Month Contract
Rate: $55-$63/hr on W2
US Citizenship / Green Card Only
We are seeking an Operations Engineer to support a product transfer project within a manufacturing environment. This role will focus on product transfer execution, process implementation, site readiness, inspection readiness, engineering documentation, and cross-functional project support.
Key Responsibilities
* Support product transfer and manufacturing site readiness activities.
* Develop and update engineering documentation, process flows, work instructions, and risk assessments.
* Assist with process validation and implementation activities.
* Support inspection readiness through measurement systems, data analysis, and training.
* Coordinate gage, fixture, and calibration management.
* Support engineering changes, system updates, router modifications, and labeling changes.
* Collaborate with Engineering, Quality, Operations, and suppliers to ensure project success.
* Identify process improvement opportunities and support risk mitigation efforts.
Required Qualifications
* Bachelor's degree in Engineering or related technical field.
* 3+ years of experience in Manufacturing, Process, or Operations Engineering.
* Experience with product transfer, process implementation, or manufacturing readiness projects.
* Knowledge of process validation (IQ/OQ/PQ), risk assessments (FMEA), and engineering documentation.
* Experience with calibration, measurement systems, inspection processes, and data analysis.
* Strong communication, problem-solving, and cross-functional collaboration skills.
Preferred
* Experience in Medical Device, Pharmaceutical, Life Sciences, or regulated manufacturing environments.
* Knowledge of FDA, GMP, and/or ISO 13485 standards.
* Experience with SAP, ERP/MES systems, MSA, Gage R&R, Lean Manufacturing, or Six Sigma.
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