Assistant Process Engineer
Listed on 2025-12-29
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Engineering
Quality Engineering, Process Engineer
Job Title: Assistant Process Engineer
Location: Devens, MA
Type: Contract
Compensation: $26.00 - $29.25 hourly
Contractor Work Model: Hybrid
Full
Job Description:
This role is responsible for assessing process-related deviations, analyzing performance data to identify trends and improvement opportunities, and providing technical support to cross‑functional teams.
- Assess the impact of process‑related deviations and provide clear, data‑driven evaluations.
- Analyze process performance data to identify trends and improvement opportunities.
- Assess trends in support calls received from the manufacturing floor to identify problem areas with the process and recommend solutions.
- Summarize and present findings effectively to audiences with varying levels of technical understanding; strong presentation and communication skills are essential.
- Verify data accuracy across multiple GMP systems; maintain strong understanding of GMP data systems and move swiftly between platforms.
- Provide on‑floor technical support for equipment and process‑related issues.
- Assist in deviation prevention and closure through site quality systems.
- Collaborate with cross‑functional teams including Scheduling, MSAT, Supply Chain, Quality, and Facilities & Engineering.
- Apply continuous improvement tools to identify and close procedural and compliance gaps.
- Perform gowning activities and enter manufacturing areas as needed.
- This position offers growth opportunities to expand into trend investigations using statistical tools (e.g., EWMA, control charts) and evaluating manufacturing capabilities for continuous improvement.
- Required Bachelor’s degree in Science or Chemical/Biological Engineering.
- Minimum 0‑2 years of industry experience; cGMP or Cell Therapy manufacturing experience preferred.
- Proficiency in Excel and JMP for data analysis.
- Experience with Tableau, Spartan, and Mareana is a plus.
- Strong technical understanding of cell therapy manufacturing processes.
- Familiarity with GMP documentation and electronic data systems.
- Technical writing skills for authoring impact assessments, SOPs, and clear documentation.
- Ability to work collaboratively in a fast‑paced environment.
- Strong problem‑solving, troubleshooting, and presentation skills.
: #558-Scientific
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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