Reagent Manufacturing Associate - Markham, Canada - Fluidigm

Fluidigm

Verified Company

Markham, Canada

13 hours ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Job Description:

Would you like to join an innovative team driven by a bold vision - _unleashing tools to accelerate breakthroughs in human health?_**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

Description:

Perform formulation of biological solutions, filtration, aliquot and packaging
Executes manufacturing validation test plans, assists with the preparation of technical reports
Ensure lab equipment is calibrated in a timely manner and maintain quality records in the Quality Assurance database
Stock and transfer finished goods between manufacturing and supply chain (physically and in ERP)
Perform cycle counts of WIP and finished goods
Troubleshoot discrepancies take corrective action
Maintain and organize the work area to keep a clean, orderly and safe work environment

Qualifications:

Bachelor's degree in Biology, Biochemistry or similar Life Science
12 years experience working in a lab environment specializing in genomic assay development and manufacturing highly desirable
Ability to read, analyze, and interpret scientific and technical reports, technical procedures, validation protocols and reports, operating instructions, and/or scientific publications.
Working knowledge of MS Office, Excel, Access and general understanding of ERP concepts
Ability to pick up new technologies quickly and ultimately troubleshoot independently
Ability to multitask in a fastpaced environment
Attention to detail is essential
Experience working in a cGMP or ISO laboratory environment.
Selfdirected, organized, and possesses good judgment

Additional Requirements:

Ability to sit, stand, move about the facility
Work performed in a combination of shipping, manufacturing and office environments
Ability to quickly familiarize with products and part numbers
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._