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QC Analyst, Microbiology (All Levels)

Lykan Bioscience
Hopkinton, Massachusetts, US
Closing date
Jun 26, 2022

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Consultancy/Private Sector
Conservation science
Genetics, Biology
Salary Type
Employment Type
Full time
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Lykan Bioscience is a fast-growing and innovative contract development and manufacturing organization (CDMO) focused on cell-based therapies. Cell therapy, one of the most transformative innovations in modern biotechnology, holds enormous potential for treating patients suffering from a variety of diseases. We are on a mission to improve patients' lives by innovating and delivering advanced cell-based therapies.


Working at Lykan is not just a job, it's an opportunity to work with a great team with diversified backgrounds and top-tier innovative biotechnology companies to contribute to the development and manufacture of revolutionary, life-saving treatments. Our team's passion for patients uniquely defines us. It's not about what we do; it's about why we do what we do.


Here at Lykan, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Innovation, Excellence, Teamwork, Integrity, Trust, and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success, at Lykan we focus on developing our corporate culture, people's development, growth, and the ability to impact patients.


The Quality Control Analyst will be responsible for collection of environmental and raw material samples, sample management activities, and testing of cell therapy in-process, release and stability product samples. He/she will be responsible for reporting of data and writing/revising standard operating procedures (SOPs). He/she may support equipment onboarding and qualification as well as test method qualification in compliance with all applicable quality systems and current cGMPs.

  • Conduct routine and non-routine analyses of samples for in-process, final product, stability, raw materials, and environmental samples.
  • Execute sampling and QC Sample Management activities per procedure or written protocols.
  • Perform environmental monitoring of cleanrooms and controlled areas
  • Complete documentation for QC testing activities including data reports, reagent preparation, equipment logs and inventory logs.
  • Write/revise QC specific procedures and protocols for newly built Cell Therapy manufacturing facility.
  • Support implementation of information technologies that support documentation and data management systems.
  • May participate in investigations, change controls and CAPAs.

  • Certificate in Biotechnology or Bachelor's degree in scientific discipline preferred
  • 0-7 years' experience in manufacturing environment
  • Familiarity/experience in a cGMP QC laboratory is desirable
  • Ability to adhere to timelines for testing and reporting of data
  • Ability to function in a team-oriented environment
  • Cell therapy analytical experience is a plus


All Lykanians embrace the principles of the Lykan Bio culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.

Lykan is proud to be an equal opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.
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