Kincell Bio · 9 hours ago
Contingent Worker, Manufacturing Associate I
Kincell Bio is a contract development and manufacturing organization focused on engineering cells into therapies, particularly in the area of immune cell therapies. As a Contingent Manufacturing Associate I, you will operate cell and gene therapy equipment, perform quality control analyses, and collaborate with the team to ensure adherence to standard operating procedures in a manufacturing setting.
BiopharmaBiotechnologyPharmaceutical
Responsibilities
Working knowledge of Word and Excel
Demonstrate Aseptic Qualification
Maintaining personal responsibility with Personal Protective Equipment (PPE)
Be a collaborator when a team develops Standard Operating Procedures or Manufacturing Batch Records
Conduct Quality Control analyses in a Manufacturing setting
Able to learn how to handle materials and bring them into a Manufacturing cleanroom
Clean Equipment and Manufacturing Suite / Rooms
Be accountable for your own Safety. Also, be accountable for maintaining your own training requirements
Collaborate with the Investigation team when investigating Quality and Safety Incidents
Author Minor Quality / Safety Incident Investigation (Deviations) and Minor CAPAs
Develop a knowledge of GXP procedures (GMP, GLP, GCP, GDP, etc.)
Must help with cleaning with Equipment and Manufacturing process rooms
Contribute to the team’s success by sharing knowledge
Review of Applicable Logbooks
Support and Conduct Enrollment of Materials / Bill of Materials
Create Purchase Requests / Procuring Items as needed
Escort Vendors / Visitors into the cleanroom
Conduct post-campaign line or area clearance
Qualification
Required
Bachelor of Science degree in Natural Sciences (i.e., Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 0-2 years of manufacturing experience required or equivalent combination of education and experience
Must be able to work 40 hours per week
Ability to work independently and stay on task in a fast-paced environment without direct supervision
Must be able to recognize when processes, procedures, equipment, products, materials, etc. are out of specification
Hiring will be contingent on passing a visual acuity test. Proof of passing a visual acuity test within the past year will be accepted
Effective oral communication
Ability to work well with others in a collaborative team environment
Regular and reliable performance and attendance are required
Able to work in a rapidly changing climate – reacts well to change
Must be able to perform mathematical calculations such as converting milliliters to liters or grams to kilograms. Understands significant figures and rounding
Must be able to lift bags and/or containers of media
Must be able to stand and/or sit for extended periods
Manage your own time and professional development. Be accountable for your own results and prioritized workflows
Preferred
Have knowledge of cell and gene therapy processing, the metric system, and scales
cGMP clean room experience
Benefits
Competitive benefits
Company
Kincell Bio
Kincell Bio collaborates with cell therapy developers by using considerable scientific experience and industry understanding.
Funding
Current Stage
Growth StageTotal Funding
$58MKey Investors
Kineticos Ventures
2025-05-15Series Unknown· $22M
2023-07-26Series A· $36M
Recent News
2026-01-15
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