Associate Ii, Quality Control

6 months ago


Vancouver, Canada Aspect Biosystems Full time

**Responsibilities**
- Support studies to assess iPSC β-cell aggregates, primary pancreatic islets, primary hepatocytes, and cell lines (Min6, Ins1, HepG2, etc.) viability in vitro and ex vivo, including the development of quantitative measures for cell viability, purity, and potency.
- Execute routine analytical assays such as ELISA, fluorescent microscopy, cytotoxicity, osmolality, viscosity, purity, rheology, and other QC Analytics functions as needed.
- Design and execute raw material and stability testing programs in coordination with quality assurance and other stakeholders.
- Help develop methods to support biomaterial QC activities such as material release and generation of Certificates of Analysis.
- Perform laboratory-based studies to qualify biocompatible materials for incorporation into bioprinted pancreatic tissues.
- Participate in assay development and validation activities for R&D and manufacturing purposes.
- Support technology transfer of analytical assays out of and into the QC Analytics team.
- Participate in laboratory and product excursion investigations (Alert, Action, and Out of Spec/Out of Trend) in coordination with Quality Assurance.
- Conduct peer review of analytical data, maintain data trending records, and execute statistical process control methods to evaluate cells, clusters, islets, and bioprinted tissue therapeutics throughout the manufacturing process.
- Support development and execution of drug substance/product process optimization and characterization projects to achieve specific project and company milestones.
- Support the production and assessment of bioprinted tissue therapeutics to Aspect's R&D and Manufacturing groups. Duties may include equipment readiness and maintenance as well as product monitoring.
- Work with the Aspect's Manufacturing, R&D, and Engineering teams to generate, optimize, and characterize analytical assays which are suitable for specific tissues/indications.
- Execute cGMP compliant documentation of analytical assays, primary/stem cell manufacturing, and biomaterial development activities in compliance with Good Documentation Practices (GDP).
- Create and maintain SOPs, batch records, and other documentation as required in compliance with GDP.
- Develop experimental protocols, update experimental reports, and present experimental data to key stakeholders.

**Qualifications**
- **Education Experience**:A master's in biomedical engineering, materials science, biochemistry, life sciences or related field, accompanied by a minimum of 2 years of industry experience; alternatively, a BSc. with at least 5 years of industry experience.
- **Professional Experience. **Moderate experience in raw material testing, development of stability programs, and assay development within a GLP/GDP environment. Additional expertise in aseptic mammalian cell culture, and bioanalytical quantification assays including ELISA is considered an asset. Experience with adherence to GLP/GDP practices.
- **Strong Analytical Skills**:Proficiency in analyzing datasets to interpret and communicate findings to key stakeholders

**Who You Are**
- **Detail-Oriented**:You have outstanding attention to detail and exhibit experimental and process rigour. You take pride in your work and strive for excellence.
- **Meticulously Organized**:You can multi-task, prioritize competing deadlines, and have a track record for delivering work on time.
- **Collaborative**:You thrive in a multidisciplinary team environment and believe that we can get further, faster, by working together. You take direction well and ask for clarification when necessary.
- **Effective Communicator**:You are an active listener who can communicate to different audiences in diverse situations.
- **Critical Thinker**:You excel at evaluating difficult challenges, seeking input from different sources, and contributing to well-informed decisions.

**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 decisio



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