Biologics Downstream Engineer - Training & Impact

Bristol-Myers Squibb; Harvard (MA); On-site; USD 55,000 - 67,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off (FTO)

Job summary

Bristol Myers Squibb in Devens, MA is hiring a Production Engineer/Scientist 1 for the Single Use Facility. This role involves mastering routine and complex manufacturing tasks, providing daily technical oversight, and training staff to maintain cGMP compliance in a state-of-the-art facility.

You will lead process improvements, guide shift personnel, and support investigations and validations, with a strong focus on safety and continuous improvement in the biologics pipeline.

Qualifications

• Education & Experience Requirements: Bachelor's degree in Engineering or Life Sciences with 0+ to 2 years in the industry.
• Required Skills: STEM knowledge, strong academics, passion for science, attention to detail.
• Desired Skills: internships/co-op in pharma or research; strong communication and leadership.

Responsibilities

• Master routine and complex manufacturing assignments with initiative.
• Provide in-depth training and ensure SOP adherence.
• Operate production equipment and process automation in downstream biologics.
• Guide less experienced personnel and ensure timely training completion.
• Lead coordination of special projects such as validation or investigations.
• Revise and create process documents.
• Champion safety and operational improvement initiatives.
• Contribute to continuous improvement through data-driven changes.

Skills

STEM knowledge

Strong academics

Passion for science

Attention to detail

Education

Bachelor's degree in Engineering or Life Sciences

Job description

Bristol Myers Squibb in Devens, MA is hiring a Production Engineer/Scientist 1 for the Single Use Facility. This role involves mastering routine and complex manufacturing tasks, providing daily technical oversight, and training staff to maintain cGMP compliance in a state-of-the-art facility.

You will lead process improvements, guide shift personnel, and support investigations and validations, with a strong focus on safety and continuous improvement in the biologics pipeline.