Manufacturing Science & Technology Associate

Crystal Equation Corporation

Westborough (MA)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

Crystal Equation Corporation is seeking a Manufacturing Science & Technology Associate to support laboratory operations, cell culture activities, and study execution in GMP-support environments.

You will handle routine MS&T duties, maintain records with data integrity, and collaborate with cross-functional teams to enable process understanding and technology transfer.

Qualifications

  • BS or MS in biology or related field with relevant lab experience.
  • Hands-on mammalian or stem cell culture experience.
  • Aseptic technique and ability to follow SOPs, batch records and study instructions.
  • Excellent documentation and data integrity.
  • Strong organizational skills to manage multiple priorities in a fast-paced lab.
  • Willingness to work onsite with occasional weekend/holiday schedules.
  • Proficiency in Microsoft Office applications.
  • Ability to collaborate with cross-functional teams.

Responsibilities

  • Manage routine MS&T laboratory operations, including organization, material inventory, supply ordering, equipment coordination, and maintenance of a safe workspace.
  • Perform mammalian and stem cell culture activities, including media preparation, cell feeding, passaging, sampling, monitoring, and documentation.
  • Execute laboratory studies in accordance with approved protocols, batch records, SOPs, and study instructions.
  • Support the preparation and review of protocols, batch records, worksheets, and technical reports through data compilation, record verification, and documentation management.
  • Collect, analyze, and summarize study data to support process understanding, troubleshooting, and continuous improvement.
  • Support commercial readiness through process readiness studies, technology transfer activities, GMP readiness initiatives, documentation updates, and cross-functional coordination.
  • Adhere to quality systems and good documentation practices, ensuring records are complete, accurate, and compliant with data integrity requirements.
  • Collaborate effectively with MS&T, Manufacturing, Quality, Process Development, and other cross-functional stakeholders to achieve project and operational objectives.
  • Provide support across laboratory, operational, documentation, and project activities based on business priorities.
  • Duties, responsibilities, and activities may change at any time with or without notice.

Skills

Mammalian cell culture
Stem cell culture
Aseptic technique
Documentation / data integrity
Lab operations management
Cross-functional collaboration
MS Office proficiency

Education

BS or MS in biology/related field

Tools

Microsoft Office

Job description

The Manufacturing Science & Technology (MS&T) Associate supports laboratory operations, cell culture activities, study execution, technical documentation, and commercial readiness initiatives. This role requires a hands-on, detail-oriented professional who applies strong organizational skills, sound documentation practices, and a collaborative mindset in laboratory and GMP-support environments.

Responsibilities
  • Manage routine MS&T laboratory operations, including organization, material inventory, supply ordering, equipment coordination, and maintenance of a safe, inspection-ready workspace.
  • Perform mammalian and stem cell culture activities, including media preparation, cell feeding, passaging, sampling, monitoring, and documentation.
  • Execute laboratory studies in accordance with approved protocols, batch records, SOPs, and study instructions.
  • Support the preparation and review of protocols, batch records, worksheets, and technical reports through data compilation, record verification, and documentation management.
  • Collect, analyze, and summarize study data to support process understanding, troubleshooting, and continuous improvement.
  • Support commercial readiness through process readiness studies, technology transfer activities, GMP readiness initiatives, documentation updates, and cross-functional coordination.
  • Adhere to quality systems and good documentation practices, ensuring records are complete, accurate, and compliant with data integrity requirements.
  • Collaborate effectively with MS&T, Manufacturing, Quality, Process Development, and other cross-functional stakeholders to achieve project and operational objectives.
  • Provide support across laboratory, operational, documentation, and project activities based on business priorities.
  • Duties, responsibilities, and activities may change at any time with or without notice.
Required Skills
  • BS or MS degree in biology, bioengineering, cell biology, biochemistry, biotechnology, or a related scientific field with relevant laboratory experience appropriate for an associate-level role.
  • Hands-on experience with mammalian cell culture and/or stem cell culture experience.
  • Good aseptic technique and ability to follow established procedures, SOPs, batch records, and study instructions accurately.
  • Strong attention to detail with demonstrated commitment to accurate documentation, record management, and data integrity.
  • Strong organizational skills with the ability to manage multiple priorities and meet timelines in a fast-paced laboratory environment.
  • Demonstrated flexibility to support laboratory operations, study execution, documentation, and related business needs.
  • Good written and verbal communication skills and ability to work effectively both independently and as part of a team.
  • Ability to work onsite and support flexible schedules, including occasional weekend or holiday work, based on cell culture or business needs.
  • Proficiency with Microsoft Office applications.
Preferred Skills
  • Experience in biotechnology, pharmaceutical, cell therapy, or GMP-regulated laboratory environments.
  • Direct experience with human stem cell culture, differentiation systems, and related analytical techniques (e.g., FCM, IFA, qRT-PCR).
  • Working knowledge of cGMP, quality systems, data integrity, and good documentation practices.
  • Experience supporting technology transfer, process characterization/qualification, or manufacturing readiness acti
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