Fluidigm

QC Associate, Gx

Job Locations CA-ON-Markham
Req No.
2023-3712
Category
Manufacturing
Type
Regular

Job Description

It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health.

At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed, and influenced by our core behaviors:

  • Keep customers front and center in all of our work
  • Be accountable and deliver on commitments
  • Drive continuous improvement
  • Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment

 

Standard Biotools is looking for a motivated Quality Control Associate to help perform QC testing of raw materials and reagents for release, stability, in-process reagent and Assay testing. The successful candidate will also participate in the development and testing of new QC procedures.

Description:

  • QC incoming raw materials, in-process testing, and final QC of oligo based products. Analyze data and complete testing reports
  • Work with R&D and Technical Support to transfer new products into Reagent Manufacturing and/or the Assay Design Group
  • Assist in the development of QC procedures, create and maintain QC documentation for new and existing products, processes, and equipment
  • Responsible for equipment calibration tracking
  • Assist manufacturing with filling/packaging events as requested


Minimum Qualifications:

 

  • BSc in Genomics, Molecular Biology or related discipline or higher
  • Experience with nucleic acid, cell culture and protein assays and/or single cell technologies are considered an asset.
  • Knowledge and experience with PCR, qPCR, DNA and RNA library preparation and next generation sequencing
  • Hands on experience with maintaining cell cultures and tissue culture techniques
  • Experience working in cleanrooms using aseptic technique is required
  • Must be able to work well both independently and in a team setting
  • Familiar with the use of MiSeq, Agilent Bioanalyzer, nanodrop spectrophotometers and Qubit, is also preferred. 

 

Ready to join an industry leader with a bold and ambitious mission that is enabling advancements in human health? Apply online with your resume!

 

 

 

The Company is committed to providing an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require an accommodation during this process, please inform The Company of your requirements.  We are an equal opportunity employer.

Internal Job Info

It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health.

At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed, and influenced by our core behaviors:
- Keep customers front and center in all of our work
- Be accountable and deliver on commitments
- Drive continuous improvement
- Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment
 
Standard Biotools is looking for a motivated Quality Control Associate to help perform QC testing of raw materials and reagents for release, stability, in-process reagent and Assay testing. The successful candidate will also participate in the development and testing of new QC procedures.

Description:
- QC incoming raw materials, in-process testing, and final QC of oligo based products. Analyze data and complete testing reports
- Work with R&D and Technical Support to transfer new products into Reagent Manufacturing and/or the Assay Design Group
- Assist in the development of QC procedures, create and maintain QC documentation for new and existing products, processes, and equipment
- Responsible for equipment calibration tracking
- Assist manufacturing with filling/packaging events as requested

Minimum Qualifications:
- Bachelor’s degree in Biology, Chemistry, or related field
- 2+ years in Biotech, Medical device, or Pharmaceutical industry
- Must have significant experience in PCR, sequencing and other Molecular Biology techniques
- Previous work in QC role
- Strong verbal and written communication skills
- Superb time management skills
 
Ready to join an industry leader with a bold and ambitious mission that is enabling advancements in human health? Apply online with your resume!
 
 
 
The Company is committed to providing an inclusive and barrier free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require an accommodation during this process, please inform The Company of your requirements.  We are an equal opportunity employer.

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