Job Description
***Please only local candidates to Devens MA
84079
TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.
Our client, a leading pharmaceutical company is hiring an Assistant Process Engineer for a 6+ months contracting assignment.
Must have skills:
- Proficiency in Excel and JMP for data analysis
- Familiarity with GMP documentation and electronic data systems
- Required Bachelor’s degree in Science or Chemical/Biological Engineering
- Minimum 0–2 years of industry experience; cGMP or Cell Therapy manufacturing experience preferred
Preferred Skills:
- 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
Pay: $28-29/hour W2
Location: Devens MA
Responsibilities:
- 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
- The position requires proficiency with data monitoring and analysis tools and the ability to verify data accuracy across multiple GMP systems
- Additional duties include assisting in deviation prevention and closure, applying continuous improvement tools, and performing gowning activities to enter manufacturing areas
- Assess the impact of process-related deviations and provide clear, data-driven evaluations
- Analyze process performance data to identify trends and improvement opportunities; experience with data monitoring systems such as Tableau, Spartan, and Mareana is a plus, as well as proficiency in Excel and JMP for data analysis
- 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
- Verify data accuracy across multiple GMP systems; maintain strong understanding of GMP data systems and move swiftly between platforms
- Provide on-the-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