Manufacturing Associate
Landmark Bio
Job Description
Job Description
We are seeking a highly motivated, team-oriented individual with a strong desire to learn and grow in a manufacturing environment. As a Manufacturing Associate, you will support the production of clinical supply products under cGMP conditions. You will play an important role in ensuring safe, high-quality, and efficient manufacturing operations while developing foundational skills in a regulated environment.
Working as part of a cross-functional team, you will contribute to day-to-day manufacturing activities, support operational readiness, and help maintain compliance with quality and regulatory standards.
Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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$17 - $26 per hour
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A leading biopharmaceutical organization in Norwood, Massachusetts is seeking a Biotech Manufacturing Associate to drive the production of innovative mRNA therapeutics and vaccines. The role requires a Bachelor’s degree in a relevant field and familiarity with cGMP regulations...Day shift- A biopharmaceutical company in Massachusetts seeks a Manufacturing Associate II for Gene Therapy Manufacturing. This role includes working on the Upstream Manufacturing area, ensuring adherence to cGMP standards, operating quality systems, and maintaining documentation....
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