Top 5 Process Engineer Associate Jobs in Allston, MA

Senior Associate Process Engineer (Contract)
ElevateBio —Waltham, MA
- $43 - $57 an hour
- Contract
- Mid-level
- 3 years
- Continuous improvement
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Associate Director, Manufacturing Systems & Automation (CGT)
Vertex Pharmaceuticals —Boston, MA
- $160,000 - $240,000 a year
- Full-time
- 7 years
- Computer Science
- Engineering
- Loan repayment program
- Dental insurance
Associate Scientific Fellow, Process Chemistry
Takeda Pharmaceutical —Cambridge, MA
- $154,400 - $242,550 a year
- Full-time
- 7 years
- Master's degree
- Bachelor's degree
- Paid holidays
- Disability insurance
2d

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The Associate Process Engineer (Drug Product) is an entry level technical contributor within Manufacturing Science and Technology (MS&T), responsible for…
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Senior Associate Process Engineer (Contract)

ElevateBio -
Waltham, MA

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Job Details

Contract
$43 - $57 an hour

Qualifications

Cell line culture
Production validation processes
Bioprocessing
Sterile products production
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full Job Description

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.

The Role:

ElevateBio is looking for a Senior Associate Process Engineer within the Manufacturing Science and Technology (MSAT) organization. As a Senior Associate Process Engineer in MSAT, you will provide process science support for GMP manufacturing, technology transfers, development studies, characterization, validation, and continuous improvement projects within a highly matrixed cross-functional team for ElevateBio programs. As part of support, you will write protocols, product impact assessments, root-cause analysis reports, and technical reports. You will additionally support data collection and charting for non-GMP and GMP batches. This position is a 6-month contract.

Here's What You'll Do:

Work cross-functionally across Process Development, Manufacturing, Quality, and Supply Chain to provide support for technology transfers and cGMP manufacturing for both clinical and commercial stage programs across modalities including cell and gene therapy, mRNA and viral vector.
Authoring and reviewing technical documentation related to manufacturing activities including protocols, technical reports, work instructions, SOPs.
Own and support quality events such as deviations, investigations, CAPAs, and Change Controls.
Assist in the root cause determination of process-related deviations in a timely and complete manner. The candidate will work with a cross-functional team to resolve complex problems using experience and efficient application of scientific methodology and technical reasoning, then propose comprehensive process solutions and improvements.
Support gap analyses and risk assessments to support the capital projects and tech transfers.

Requirements:

Bachelor's Degree in Life Sciences, Engineering, Biotechnology, or a related technical discipline
3+ years of experience in a MSAT, Manufacturing, or Process Development role
Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture, and process development
Experience in cell and gene therapy, aseptic processing, and drug manufacturing preferred
Understanding of process development, validation, and lifecycle management to support comparability studies, process validation, and licensure changes
Strong communication skills and ability to work cross-functionally with technical and quality teams
Familiarity with electronic systems used in GMP environments such as Veeva, or electronic batch records

The budgeted range for this position is $43/hour - $57/hour. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.

ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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Process Engineer Associate jobs in Allston, MA

Senior Associate Process Engineer (Contract)

Associate Director, Manufacturing Systems & Automation (CGT)

Associate Scientific Fellow, Process Chemistry

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