Quality Control Associate

ZEO ScientifiX; Fort Lauderdale (FL); On-site; USD 52,000 - 78,000; Full time

Job summary

ZEO ScientifiX is seeking a Quality Control Associate to perform technical and quality procedures within our Quality Management Program for the manufacturing and drug development laboratory in South Florida. The role involves supporting biologic drug manufacturing quality control operations and ensuring data integrity and GDP compliance.

Qualified candidates have a BS/MS in Biomedical Sciences or related fields, strong writing and communication skills, and experience with quality systems in

Qualifications

• Experience in biomedical tissue manufacturing quality systems.
• BS or MS in Biomedical Sciences or related fields.
• Motivated with professional etiquette.
• Strong writing skills.
• Excellent organizational skills.
• Strong communication with internal and external stakeholders.
• Comfortable with computers and digital communication.

Responsibilities

• Manage quality control activities involved with biologic drug manufacturing and facility quality control operations.
• Oversee and review facility operation practices, complete and review product testing procedures, perform material receipt and inspection, and complete equipment management and monitoring.
• Work jointly with the lab team to ensure facility compliance and maintain operational standards for cell and biologic manufacturing.
• Ensure compliance with regulatory standards (FDA, EMA, CLIA, GLP, GMP).
• Ensure data integrity and adherence to Good Documentation Practices (GDP).

Job description

ZEO ScientifiX is looking for a Quality Control Associate

ZEO ScientifiX is a clinical stage biotechnology company developing cell and extracellular vesicle-based therapeutics. ZEO ScientifiX is seeking a Quality Control Associate to perform technical and quality procedures within our Quality Management Program for the manufacturing and drug development laboratory.

Responsibilities of the Quality Control Associate include a variety of technical activities involved with biologic drug manufacturing and quality assurance/control operations.

South Florida local applicants are encouraged to apply

Responsibilities:

• Manage quality control activities involved with biologic drug manufacturing and facility quality control operations.
• In general, oversee and review facility operation practices, complete and review product testing procedures, perform material receipt and inspection, and complete equipment management and monitoring.
• Work jointly with the lab team to ensure facility compliance and maintain operational standards for cell and biologic manufacturing.
• Ensures compliance with regulatory standards (e.g., FDA, EMA, CLIA, GLP, GMP)
• Ensures data integrity and adherence to Good Documentation Practices (GDP)

Qualifications:

• Must have prior experience in a biomedical / tissue manufacturing quality systems operation
• B.S. or M.S. in Biomedical Sciences or related sciences are encouraged to apply
• Must be highly motivated with professional etiquette
• Must be a skilled writer
• Have excellent organizational skills
• Have strong attention to detail
• Strong communication skills with internal and external individuals
• Must be comfortable working with computers and digital communication

Job Type:

Full Time

Education:

Bachelor of Science (BS) degree or Higher (required)