Production Quality Control Technician I

Socket.dev; Miami (FL); On-site; USD 42,000 - 60,000; Full time

Job summary

VIVEX Biologics, Inc. is seeking a Operations Production Quality Control Technician I to review tissue processing documentation and ensure compliance with QA requirements. The role includes uploading records, archiving documentation, and verifying electronic records across allograft production.

Responsibilities cover batch record review, data entry accuracy, and coordination with QA for disposition. Strong attention to detail and communications with multidisciplinary teams are essential.

Qualifications

• Bachelor’s degree in science or related field, or associate degree with relevant experience.
• 0–1 year of relevant experience preferred.
• Tissue Banking experience preferred.
• Strong analytical, planning, critical thinking and troubleshooting skills.
• Ability to communicate effectively with multidisciplinary teams.

Responsibilities

• Reviews for correction and completeness of batch records for allografts/autografts.
• Reviews data entry and spreadsheets generated during production.
• Coordinates timely review of product batches prior to QA disposition.
• Maintains batch record and labeling spreadsheets.
• Archives VRL culture documentation and handles nonconformance inquiries.
• Issues and verifies electronic Signature Acknowledgement forms for processing personnel.
• Reviews and catalogs logs from cleaning of production rooms.
• Reviews and catalogs logs for sterilization of goods.
• Uploads Tissue Receipt Forms.
• Ensures processing documentation complies with state/federal regulations and AATB standards.
• Understands urgency for customer delivery and quality during document review and archiving.
• Uses judgment to identify and resolve production QC flow interruptions.
• Completes daily tissue processing documentation reviews.
• Performs other duties as needed or directed by management.

Skills

Analytical thinking

Troubleshooting

Communication skills

Attention to detail

Education

Bachelor’s degree in science or related field

Associate degree with relevant experience

Tools

Computer Processing

Job description

Description

The Operations Production Quality Control Technician I reviews and inspects documentation requirements of tissue during all steps of processing of Musculoskeletal tissue and Birth tissue. The Production Quality Control Technician I also reviews documentation for the cleaning of processing rooms and documentation for the sterilization of goods used in the production of allografts. The Production Quality Control Technician I will also verify documentation against electronic records and upload Tissue batch and labeling batch records into electronic form. The Production Quality Control Technician I will also archive documentation complying with Quality Assurance requirements as mandated by federal, state, and trade regulations.

Requirements

Applicants must be legally authorized to work in the United States. Vivex will not provide sponsorship or employment for candidates who require the 24-month STEM Optional Practical Training (OPT) extension. Please note this is not an offer of immigration sponsorship

Duties and Responsibilities

1. Reviews for correction and completeness of all batch records generated during the production of allografts and Autografts.

2. Reviews for correction and completeness all data entry and corresponding spreadsheets generated in the production of allografts and Autografts.

3. Coordinates for a timely review and correction of all generated product batches prior to submission to QA for final review and disposition.

4. Responsible for entry and maintenance of Batch record Spreadsheet and Labeling batch Spreadsheet

5. Responsible for review and archiving of VRL accession culture documentation as well as, responding to or properly directing request for clarification and nonconformance of testing request.

6. Responsible for issuing and verifying FM GEN 2 (Electronic Signature Acknowledgement form) for Processing personnel.

7. Reviews and catalogs all logs generated in the cleaning of Production clean rooms

8. Reviews and catalogs all logs generated in the sterilization of sterilized goods used in the production of allografts.

9. Reviews and uploads Tissue Receipt Forms.

10. Ensures that Processing Documentation comply to State and Federal Regulations and AATB Standards.

11. Understands and able to work under a challenging sense of urgency for customer delivery and Quality Standards during Document Review, uploading and archiving.

12. Uses Judgment to identify, troubleshoot and resolve day-to-day Production Quality Control flow interrupters.

13. Resourceful in completing assigned deadlines and can multitask effectively.

14. Responsible for completion of the daily review of documentation of tissue Processing.

15. Perform other duties as assigned on an as needed or emergency basis, and as assigned by Manager or Supervisor

Qualifications

Bachelor’s degree in science or related with a minimum of 0-1-year relevant experience or associate degree with 1 or more years of relevant experience, preferred. Tissue Banking experience Preferred. Strong analytical, planning critical thinking, and troubleshooting skills. Ability to effectively communicate with multidisciplinary teams.

Qualifications include

• Computer Processing
• Problem Solving
• Strong Interpersonal and organizational skills
• Good documentation skills
• Written, Verbal and strong communication skills
• Attention to detail

Working Conditions

Majority of the work is performed indoors in an office environment.

Physical Requirements

The ability to Sit for extended periods of time. Regular lifting/carrying light objects up to 10 pounds.

Direct Reports

No Direct Reports.

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job any time.

VIVEX Biologics, Inc. is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

VIVEX Biologics, Inc. complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.