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Production Quality Control Technician I

VIVEX BIOLOGICS INC
Posted a day ago, valid for 13 days
Location

Miami, FL, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The Operations Production Quality Control Technician I is responsible for reviewing and inspecting documentation related to the processing of Musculoskeletal and Birth tissues.
  • Candidates must possess a Bachelor’s degree in science or a related field with 0-1 years of relevant experience, or an associate degree with at least 1 year of relevant experience.
  • The position requires strong analytical, planning, critical thinking, and troubleshooting skills, along with effective communication abilities.
  • Working primarily indoors, the role involves light lifting and requires attention to detail while performing documentation reviews and uploads.
  • Salary details are not specified, and candidates must be authorized to work in the U.S. without requiring sponsorship.

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. 





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