Process Engineer

Alexander Technology Group; Billerica (MA); On-site; USD 55,000 - 69,000; Full time

Job summary

Alexander Technology Group seeks a Back Process Engineer QA Analyst (Hardware) in Billerica, MA. This role supports radiopharmaceutical manufacturing with hands-on cGMP experience, ensuring compliance and continuous improvement.

The candidate will lead investigations, author technical docs, and collaborate across Manufacturing, QA, QC, and Supply Chain to ensure timely, compliant campaigns. 6+ years in sterile manufacturing and strong data analysis skills are essential.

Qualifications

• Bachelor’s degree in a technical field required.
• 6+ years in medical device manufacturing, with sterile injectable or radiopharmaceutical focus preferred.
• Strong knowledge of cGMPs, aseptic processing, cleanroom operations, and related regulations.
• Demonstrated ability to investigate deviations, apply root cause analysis, and implement changes within a quality system.
• Hands-on experience with equipment used in sterile fill/finish operations.
• Experience leading process validation, equipment qualification, and risk management efforts.

Responsibilities

• Provide day-to-day technical support to manufacturing operations.
• Lead investigations of deviations and implement CAPAs with QA and operations.
• Author and revise manufacturing docs, reports, protocols, and risk assessments.
• Support process monitoring, data analysis, and continuous improvement.
• Participate in cross-functional teams for process changes and validations.
• Lead technical transfers, scale-ups, and lifecycle projects.

Skills

Problem solving

Data analysis

Technical writing

Communication

Education

Bachelor’s degree in Chemical Engineering or related

Advanced degree preferred

Tools

TrackWise

CATSWeb

Excel

Job description

Back Process Engineer QA Analyst (Hardware) Billerica , Massachusetts Temp to Perm Per Hour Aug 19, 2026 $50.00 - $60.00

Position Summary:

Client is seeking an experienced and driven Process Engineer to support key functions for radiopharmaceutical manufacturing which includes product support, process support, process engineering, equipment/utility engineering, maintenance programs, and technical troubleshooting in support of automated manufacturing lines. The individual brings hands-on experience in cGMP manufacturing support, with a strong understanding of sterile drug production, radiopharmaceutical workflows, and medical device quality systems.

Key Responsibilities:

• Provide day-to-day technical support to manufacturing operations, ensuring reliable production.
• Lead investigations for moderate- to high-complexity deviations, perform root cause analyses, and implement CAPAs in collaboration with QA and operations teams.
• Author and revise controlled documents, including manufacturing documentation, technical reports, protocols (e.g., process validation, equipment qualification), and risk assessments.
• Support process monitoring, trending, and data analysis activities to drive continuous improvement and maintain a state of control.
• Participate in cross-functional teams for process changes, equipment upgrades, and lifecycle projects, ensuring alignment with regulatory and quality requirements.
• Act as a technical contributor in change control execution, including impact assessments, protocol generation, and implementation planning.
• Support and/or lead multiple technical transfers, scale-ups, and process validation activities.
• Collaborate with stakeholders in Manufacturing, QA, QC, Engineering, and Supply Chain to ensure timely and compliant execution of manufacturing campaigns.
• Ensure compliance with applicable regulations, including 21 CFR Parts 210, 211, 820, EU GMP Annex 1, and radiation safety requirements.
• Support readiness activities for internal and regulatory audits, including documentation review and SME participation.

Qualifications:

• Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Nuclear Engineering, Chemistry, or a related technical field (advanced degree preferred).
• 6+ years of experience in medical device manufacturing, with a strong focus on sterile injectable or radiopharmaceutical production. is a plus.
• Solid understanding of cGMPs, aseptic processing, cleanroom operations, and medical device/combination product regulations (21 CFR 210, 21 CFR 211, 21 CFR 820, ISO 13485).
• Demonstrated ability to investigate deviations, problem solve, and execute changes within a quality system framework. Advanced technical writing skills required.
• Hands-on experience with equipment commonly used in sterile fill/finish operations.
• Demonstrated ability to lead process validation, equipment qualification, and risk management effor
• Self-starter with strong interpersonal and communication skills; able to work independently and in cross-functional teams.
• Proficiency in Excel, data analysis tools, and electronic document/change control systems (e.g., TrackWise, CATSWeb). Skilled at presenting technical content to technical and non-technical audiences.

Preferred Experience:

• Expereince with lean manufacturing principles and driving process improvements in any scale.
• Experience in lifecycle management of commercially approved pharmaceutical products and devices.
• Experience in managing large cross-functional projects in a matrix environment.

Pay range $40-$50/hr