Assistant Process Engineer #26-25289
us tech solutionsDevens, MA
Assistant Process Engineer #26-25289
us tech solutionsDevens, MA
today
Industries
Research and Development in Biotechnology (except Nanobiotechnology)Temporary Help ServicesOther Scientific and Technical Consulting ServicesAbout the role
Duration: 6 months contract (with extension possibility)
Job Description: Minimum 50% onsite required
Work Schedule: Mon-Fri(normal business hours)
Duration:
6 months(Possibility of extension for the right candidate depending on performance and budget)The MSAT Process Engineering Contractor will support Manufacturing Science and Technology (MSAT) activities. There will be a focus on Out-of-Specification (OOS) investigations.
Must Haves:
Required Bachelor's degree in Chemical Engineering, Biochemical Engineering, Chemistry, or related technical discipline. Minimum 0-2 years of industry experience; cGMP or Cell Therapy manufacturing experience Technical writing skills for authoring impact assessments and out-of-specification investigations. Strong problem-solving, troubleshooting, and presentation skills. Familiarity with GMP documentation and electronic data systems. Ability to work collaboratively in a fast-paced environment. Strong analytical and critical-thinking skills with attention to detail. Effective communicator, able to work cross-functionally with Quality, Manufacturing, and Engineering stakeholders.
Job Responsibilities:
Support OOS investigations; may take on investigation ownership as appropriate. Review batch records, process data, equipment logs, and analytical results to support investigation findings. Partner with Quality Assurance, Quality Control, Manufacturing, and Engineering teams to gather data and align on investigation scope and conclusions. Present investigation findings and technical rationale to cross-functional teams and management as required.
Qualifications:
Required Bachelor's degree in Chemical Engineering, Biochemical Engineering, Chemistry, or related technical discipline. Minimum 0-2 years of industry experience; cGMP or Cell Therapy manufacturing experience. Strong technical understanding of cell therapy manufacturing processes(Preferred)Technical writing skills for authoring impact assessments and out-of-specification investigations. Strong problem-solving, troubleshooting, and presentation skills. Familiarity with GMP documentation and electronic data systems. Ability to work collaboratively in a fast-paced environment. Strong analytical and critical-thinking skills with attention to detail. Effective communicator, able to work cross-functionally with Quality, Manufacturing, and Engineering stakeholders.
About US:
Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com. US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring. IND01
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JOB OVERVIEW
Experience level
Senior
Location
Devens, MA
Occupation
Validation Engineers
Industry
Research and Development in Biotechnology (except Nanobiotechnology)
Posted
today
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