Landmark Bio

manufacturing

ManufacturingAssociate

Watertown, Massachusetts, United States FULL TIME
The Brief

“Manufacturing Associate at Landmark Bio. Skills: process management, cross-functional coordination, vendor/stakeholder management, operational metrics, resource planning, continuous improvement. Support manufacturing operations to produce clinical supply products under cGMP conditions in a Lean Manufacturing environment. Execute routine production activities following batch records, standard operating procedures (SOPs), and work instructions”

What You'll Achieve.

support the production of clinical supply products; ensuring safe, high-quality, and efficient manufacturing operations; support production goals; support a culture of operational excellence

Industry & Context.

manufacturing
Problems you'll solve

Identify, document, and communicate deviations, non-conformances, or safety concerns

Eligibility Requirements

Ability to work in a cleanroom environment and wear appropriate personal protective equipment (PPE), Flexibility to support shift-based operations, including evenings, weekends, or overtime as needed

What They're Looking For.

Must Have

High school diploma or equivalent, 0–2 years of experience in manufacturing, biotechnology, pharmaceutical operations, or a related field, attention to detail and ability to follow written and verbal instructions, Ability to work in a cleanroom environment and wear appropriate personal protective equipment (PPE), Flexibility to support shift-based operations, including evenings, weekends, or overtime as needed

Nice to Have

Associate’s or Bachelor’s degree in Science or Engineering, Basic understanding of GMP and regulated environments

What You'll Do.

Support manufacturing operations to produce clinical supply products under cGMP conditions in a Lean Manufacturing environment

Execute routine production activities following batch records

standard operating procedures (SOPs)

and work instructions

and clean equipment and manufacturing areas in accordance with established procedures

Accurately document manufacturing activities in compliance with GMP and company requirements

Adhere to all safety guidelines

environmental health standards

Assist with material handling activities

and inventory tracking

and communicate deviations

Contribute to continuous improvement initiatives and support a culture of operational excellence

Support manufacturing area readiness for production activities and inspections

How You'll Work.

Team & Collaboration

Working as part of a cross-functional team, you will contribute to day-to-day manufacturing activities; Collaborate with cross-functional teams, including Quality Assurance and Manufacturing Sciences, to support production goals

Communication Scope

Effective communication and interpersonal skills

Free ATS check

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