Senior Associate, Biomaterials CMC

at  Aspect Biosystems

Vancouver, BC, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate05 Oct, 2024USD 88000 Annual05 Jul, 20245 year(s) or aboveTissue Engineering,Chemical Engineering,Medical Devices,Pharmaceutical Industry,Materials Science,Biomaterials,Pharmaceutical SciencesNoNo
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Description:

We are seeking a Senior Associate, Biomaterials CMC to join our technical operations team. This role is critical in advancing the development and scale-up of biomaterials essential for the development of our bioprinted tissue therapeutics. Working closely with the Chief Technology Operations Officer and cross-functional teams, the Senior Associate will play a key role in the Chemistry, Manufacturing, and Controls (CMC) department, ensuring the seamless transition of biomaterials from research and development into manufacturing for our bioprinted therapeutics. The contributions made in this position will have a profound impact on the future of healthcare by enabling the creation of bioprinted tissues that have the potential to revolutionize the treatment of currently incurable diseases.

QUALIFICATIONS

  • Education: Bachelor’s or Master’s degree in chemical engineering, materials science, pharmaceutical sciences, or related discipline.
  • Professional Experience: You have 5+ years’ experience in a CMC role within the biotechnology, medical device, or pharmaceutical industry
  • Biomaterials Expertise: Demonstrated hands-on experience with biomaterials, particularly in their application to drug delivery systems, medical devices, or tissue engineering. Proficiency in formulation development, process scale-up, and techniques for biomaterial characterization.

WHO WE ARE

Aspect Biosystems is a Canadian biotechnology company creating bioprinted tissue therapeutics to transform how we treat disease. Our bold team of innovators and entrepreneurs have joined us from all over the globe to create a new class of regenerative medicine and work towards a future where our bioprinted tissues are used to save lives and make people healthier. We are endlessly curious and wildly passionate about what we do. Every person on our team is a key contributor to our success and is eager to roll up their sleeves to make a difference in the ever-changing world of biotech. If you are committed to making a real impact and accelerating the development of life-changing therapies, we want to hear from you!
Curious about our current perks and benefits? Learn more here.
At Aspect Biosystems, our strength has always been in our diversity. Different people, thinking differently, unified in creating a world that is better for us all. We are committed to creating an inclusive environment for everyone on our team. All aspects of employment — including the decision to hire, promote, discipline, or terminate — are based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, colour, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, provincial, or local law.
If you’re interested in joining our team but don’t see a job posting that matches your experience or background, we encourage you to submit a general application to be considered for future opportunities

Responsibilities:

  • Support the development and optimization of biomaterial formulations and processes.
  • Work closely with cross-functional teams to transfer processes from research to process development and to GMP manufacturing.
  • Conduct experimental work and data analysis to support process development and troubleshooting.
  • Participate in the qualification of vendors and biomaterials.
  • Maintain comprehensive and accurate records of experiments, protocols, and results.
  • Prepare and review technical reports, protocols, SOPs, and other CMC documentation.
  • Develop and implement CMC strategies for our biomaterials.
  • Participate in risk assessment and mitigation strategies for CMC development.
  • Identify opportunities for process improvement and contribute to the implementation of best practices.
  • Ensure compliance with regulatory requirements and quality standards
  • Communicate project progress and challenges effectively with team members and stakeholders.
  • Collaborate with internal and external partners to support CMC activities.


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Information Technology/IT

IT Software - Other

Software Engineering

Graduate

Chemical, Engineering

Proficient

1

Vancouver, BC, Canada