Process Engineer II

We are looking for Process Engineer II for our client in Framingham, MA

Job Title: Process Engineer II

Job Location: Framingham, MA

Job Type: Contract

Job Overview:

Pay Range: $60.95/hr - $65.95/hr

Requirement/Must Have:

• Bachelor's degree in Chemical Engineering, Biochemistry, Biotechnology, Bioengineering, or a related life sciences field with a minimum of 2+ years of relevant industry experience; OR a Master's degree with a minimum of 1+ years of experience in biopharmaceutical manufacturing, process engineering, or process development.
• Familiarity with upstream and/or downstream bioprocess unit operations (e.g., cell culture, chromatography, filtration) and GMP manufacturing environments.
• Working proficiency in Microsoft Excel; comfort with data review, process trending, and technical documentation systems.
• Strong attention to detail, organizational discipline, and the ability to manage multiple priorities within defined timelines.
• Effective written and verbal communication skills in a cross-functional team setting.

Responsibilities:

• Support technology transfer activities by collecting, organizing, and maintaining process data, batch records, and technical documentation throughout transfer planning and execution phases.
• Perform data verification, reconciliation, and integrity checks to ensure process information is accurate, traceable, and fit for technical review and regulatory reporting.
• Maintain and update process trackers, study logs, document repositories, and readiness dashboards used to monitor transfer milestones and action items.
• Conduct routine data trending, charting, and analysis to support process monitoring, flag potential inconsistencies, and surface opportunities for process improvement.
• Assist in preparing technical summaries, transfer reports, gap assessments, presentations, and cross-functional meeting materials in support of senior engineers and program leads.
• Support investigation and deviation activities by compiling relevant process data, organizing supporting documentation, and coordinating information requests across functions.
• Contribute to digitalization and data modernization efforts, including the development or maintenance of dashboards, structured data templates, automated trackers, and workflow tools (e.g., Excel-based tools, Power BI, or similar platforms).
• Participate in cross-functional meetings and facilitate clear communication of data findings, open action items, and transfer status updates.

Nice to Have:

• Prior exposure to technology transfer, process characterization, process validation, or manufacturing support activities in a GMP biologics setting.
• Experience with data visualization tools, process analytics platforms, or digital workflow development.
• Familiarity with quality systems including deviations, CAPAs, change controls, and investigation documentation.
• Exposure to external manufacturing partnerships or CDMO collaboration models.
• Experience across multiple biologic modalities (e.g., mammalian, microbial, etc.).