Process Development Technician

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

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Mental health support

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Childcare support

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Learning budget

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Verification

Not verified last checked Jun 13, 2026

Salary

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401(k) match

Listed Source: EMPLR_CONTRIB_INCOME_AMT. source Last checked Jun 13, 2026.

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Schedule

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Weekend work

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Application

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Deadline

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About this role

Process Development Technician Waltham, MA, United States Position Summary: The Process Development Technician - Oral Solid Dosage supports the execution of experimental studies to develop well-understood, robust oral solid dosage (OSD) manufacturing processes. Key responsibilities include equipment setup, cleaning, troubleshooting, execution of experiments, and data collection to identify and implement process and equipment improvements that reduce waste and increase process reliability. This role plays a key part in maintaining GMP standards within the pilot facility and supporting the manufacture of clinical supplies. Responsibilities: Support the set up and operation of a new GMP clinical manufacturing suite with a broad range of processing capability and technology approaches. Operate, maintain, and troubleshoot a variety of process equipment, rapidly assimilating and applying new technologies as introduced. Perform equipment and room cleaning in compliance with established housekeeping and GMP standards. Assist in designing experimental programs and compiling data from studies. Execute experiments to enhance process understanding and manufacture GMP clinical batches at various scales. Complete all documentation accurately and legibly, ensuring compliance, and participate in updating batch paperwork and SOPs. Maintain a working knowledge of Manufacturing, Quality, and Development systems and procedures; support regulatory inspections and audits as required. Maintain awareness of project schedules and strive to achieve whilst responding positively and flexibly to changing priorities to ensure desired outcomes. Assist with root cause investigations and the implementation of CAPAs, as appropriate. Ensure compliance with all applicable cGMP, safety, environmental regulations, and company policies. Take ownership of the general upkeep of process areas and

Read the full description at hbap.fa.us1.oraclecloud.com. FewerJobs shows a source-linked preview and links to the original posting.