Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Production Technician I

Job

Extremity Care

San Diego, CA (In Person)

Full-Time

Posted 2 weeks ago (Updated 1 week ago) • Actively hiring

Expires 6/28/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
62
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Purpose The Production Technician I is responsible for developing and maintaining proficiency in human tissue manufacturing procedures and related support processes to execute and sustain the production schedule. This role requires strict adherence to FDA regulations, industry standards, and Good Manufacturing Practices (GMP). Responsibilities Complete assigned training on standard operating procedures (SOPs) by required deadlines Maintain competency in aseptic technique and sterile field protocols through ongoing training Manufacture finished products from human tissue using aseptic technique in compliance with SOPs Apply good judgment to optimize tissue processing efficiency and maximize product yield Identify and report deviations and nonconformances to management and Quality Assurance Perform cleanroom and equipment cleaning, decontamination, calibration, and environmental monitoring Decontaminate, wrap, and autoclave reusable manufacturing supplies in accordance with SOPs Accurately and concurrently document manufacturing processes and support tasks in controlled records Ensure all documentation complies with GDP, SOPs, and regulatory requirements Report to work on-site and on time for scheduled shifts, including mandatory overtime when required Attend all scheduled meetings, training sessions, and appointments as assigned Maintain a working knowledge of
FDA 21 CFR 1271, FDA 21 CFR 820, AATB
standards, ISO Standards, cGMP/CGTP, other relevant regulations/standards, and internal organizational policies and standard operating procedures. Perform other duties as assigned Skills Ability to work independently and in a team environment Excellent attention to detail and organization Excellent written and verbal communication Highest level of ethics and integrity Ability to lead and motivate the right behaviors Ability to multi-task and work in a fast-paced environment Proficient in aseptic technique Excellent documentation accuracy Proficiency in Microsoft Office Ability to follow SOPs and regulatory guidelines with precision Physical Requirements Ability to work seated or standing for 8 - 10 hours Ability to lift, push, pull or otherwise transport objects or weighing up to 25lbs Qualifications/Requirements High school diploma or equivalent required At least 1 year of hands-on experience with aseptic technique required Experience working in an FDA-regulated environment preferred A higher level of education (such as an associate's or bachelor's degree in a related field) may be considered in lieu of 1-3 years of required experience Clearance of favorable background investigation required The compensation range listed reflects the full salary range for the position and is not indicative of the starting salary. Final compensation will be determined based on job-related factors, including experience, qualifications, and internal equity.