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Home Flexible Job Board Technician, THV Tissue Processing (2nd Shift)

$26.60/hr 99d ago

Technician, THV Tissue Processing (2nd Shift)

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JENAVALVE TECHNOLOGY INC

Irvine, CA, US

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Summary

Responsible for processing porcine pericardium tissue to manufacture heart valve devices within a controlled cleanroom. Tasks include chemical treatment, screening, cutting, and performing inspections according to strict regulatory and quality procedures.

Job Description

Job DetailsJob Location: Irvine, CA 92618Position Type: ContractorEducation Level: High SchoolSalary Range: $26.60 - $26.60 HourlyJob Title: Technician, THV Tissue Processing 

Technician I, THV Tissue Processing
Technician II, THV Tissue Processing
Technician III, THV Tissue Processing

Role Level: Individual Contributor

Supervisor/Manager Title: Senior Supervisor, Tissue Processing

Job Location & Environment: Irvine, CA – Corporate Office / Controlled Cleanroom Environment

Job Description Summary: 

Manufacturing - Hourly / Assembly / Inspection.
Manufacturing technician responsible for processing porcine pericardium tissue required to manufacture heart valve devices. Support for manufacturing and R&D tasks associated with new product development and commercialization of transcatheter heart valves.
This requires high manual dexterity, attention to detail, and adherence to strict regulatory, quality, and contamination control procedures within a controlled cleanroom manufacturing environment

Job Responsibilities: 

Execute receiving, chemical treatment, screening, cutting, measurements and inspection for Porcine Pericardium tissue per JVT released procedures. 
Use of tools – blades, scissors, forceps, dies, magnifying lamp – to perform tissue processing.
Use of equipment – fume hood, thickness gauges, press machines, Litematics – to perform tissue processing.
Perform verifications, against specifications, of completed steps, and execute work in assembly line.
Review, follow, and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records.
Support activities correspond to other work procedures, as requested, to provide support to operations processes.
Assist Engineering in root cause analysis investigation for component nonconformance.
Maintain compliance with company Quality Management System requirements, including applicable Good Manufacturing Practices (GMP) and regulatory standards.
Maintain reliable and consistent attendance to support production operations, including punctual arrival and the ability to work full scheduled shifts and overtime as required to meet operational and production needs.
Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others.
Other incidental duties: General work area housekeeping.

 
QualificationsRequired Education and Experience: 

The level of this role (Technician I, II, III) will be determined based on the candidate's experience, technical skills, and demonstrated competencies relevant to the position. 
Specific expectations for each level are further defined in the Technical & Operational Competency Matrix. 
High school diploma or equivalent required. Candidates without a diploma may demonstrate equivalent competency through a validated external assessment designed to evaluate comprehension, language, and related abilities at a high school level.
Previous biological tissue processing, GMP, clean room, medical device experience preferred.

Technician I:

Performs standard production tasks independently while following established work instructions, SOPs, and safety requirements with consistent accuracy and reliability.
Maintains required productivity and quality standards while completing documentation and process steps with minimal errors.
Communicate effectively with team members and supervisors while contributing to a collaborative work environment and maintaining reliable attendance and professional conduct.
Perform verifications, according to specifications, of completed steps, as well as successive reviews of steps performed by team members on their own
Is able to perform at least 4 of the core processes in addition to minimum one of the complex processes such as – BBR, leaflet cut, laser machine operation, with minimal trainer or lead verification.

Technician II: 

Executes more complex production tasks with increased efficiency and accuracy while ensuring adherence to SOPs, quality standards, and safety practices.
Identifies minor process issues or deviations and communicates them appropriately to leads or supervisors to support continuous improvement and operational reliability.
Actively supports team performance through effective communication, consistent productivity, and reliable documentation of manufacturing activities.
Perform verifications, according to specifications, of completed steps, as well as successive reviews of steps performed by team members on their own
Is able to perform at least 4 of the core processes in addition to minimum two of the complex processes such as – BBR, leaflet cut, laser machine operation or leaflet deflection; with minimal trainer or lead verification.

Technician III: 

Demonstrates mastery of tissue processing operations and independently performs complex or specialized tasks while maintaining high standards of quality, safety, and productivity.
Maintains required productivity and quality standards while completing documentation and process steps with minimal errors.
Applies strong process knowledge to ensure accurate execution of procedures, assist with troubleshooting, and help prevent recurring errors. 

Ability to find faults and correct GDP issues with minimal lead or supervisor verification.
Serves as a trusted technical resource to peers by sharing best practices, supporting team coordination, and maintaining exemplary reliability and professionalism.
Perform verifications, according to specifications, of completed steps, as well as successive reviews of steps performed by team members and ability to provide feedback to coworkers.

Skills and Abilities Required for This Job: 

Ability to use small hand tools, steady hand-eye coordination, and high manual dexterity/fine motor skills.
Must have ability to perform detailed tasks accurately.
Must be able to handle animal tissue and wet processes.
Must be able to work effectively and collaborate within cross functional teams.
Ability to read, comprehend and speak English, and good communication skills required.
Knowledge of and adherence to Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing.
Successful completion of required training and demonstrated competency on assigned manufacturing processes. 
Adhere to all rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.
Basic computer skills.

Physical Requirements: 

Ability to perform highly detailed tissue processing operations while seated or standing for extended periods during the work shift.
Ability to use hands and fingers for fine manipulation of biological tissue components, 
Ability to perform work requiring close visual acuity.
Ability to work in a controlled cleanroom environment while wearing full cleanroom gowning including gown/coveralls, gloves, mask, hairnet, boot covers, and other PPE as needed. 
Ability to follow strict safety, contamination control, and cleanroom protocols.
Must be able to stand, walk, and sit for prolonged periods of time.
Must be able to push, pull, twist, climb, balance, stoop, kneel, and crawl. 
Must be able to perform repetitive motions such as reaching and grasping. 
Ability to lift or move materials up to 25 pounds.

About the company

JENAVALVE TECHNOLOGY INC

JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR).

The JenaValve Trilogy Heart Valve System is the first and only device currently approved in the EU for the treatment of severe, symptomatic aortic regurgitation in patients that are deemed high-risk for surgical aortic valve replacement. The Trilogy System is also CE-Mark approved for treatment of severe, symptomatic aortic stenosis.

In the US, JenaValve has completed enrollment of the ALIGN-AR IDE Clinical Trial which will support a future PMA submission. If approved, the Trilogy System would become the first and only TAVR system in the US indicated for the treatment of symptomatic, severe AR.

JenaValve is headquartered in Irvine, California with offices in Leeds, U.K. and Munich, Germany.

Founded

2013

Company size

51-200 employees

Industry

Healthcare

Org type

Privately Held

Headquarters

Irvine, CA

Apply Now

About the company

JENAVALVE TECHNOLOGY INC

JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR).

The JenaValve Trilogy Heart Valve System is the first and only device currently approved in the EU for the treatment of severe, symptomatic aortic regurgitation in patients that are deemed high-risk for surgical aortic valve replacement. The Trilogy System is also CE-Mark approved for treatment of severe, symptomatic aortic stenosis.

In the US, JenaValve has completed enrollment of the ALIGN-AR IDE Clinical Trial which will support a future PMA submission. If approved, the Trilogy System would become the first and only TAVR system in the US indicated for the treatment of symptomatic, severe AR.

JenaValve is headquartered in Irvine, California with offices in Leeds, U.K. and Munich, Germany.

Founded

2013

Company size

51-200 employees

Industry

Healthcare

Org type

Privately Held

Headquarters

Irvine, CA

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