Production Technician I (Human Tissue Processing) - Bravo Shift

Extremity Care

San Antonio, TXOn-siteFull time
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Pay
$21
an hour
Location
San Antonio, TX
Work style
On-site
Job type
Full time
Posted
Oct 13
7 days ago
Career path

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About the company

Extremity Care

Biotechnology · 11 to 50 employees

Extremity Care on LinkedIn

What you'll do

  • Manufacture finished products from human tissue using aseptic technique, and perform cleanroom and equipment cleaning, decontamination, calibration, and environmental monitoring.
  • Maintain accurate controlled records and report deviations and nonconformances.

What you need

  • Requires a high school diploma or equivalent and at least 1 year of hands-on experience with aseptic technique; a related associate's or bachelor's degree may substitute for the experience.
  • Education: a high school diploma, an associate degree or a bachelor's degree

Key skills

Aseptic techniqueSterile field protocolsMicrosoft OfficeAttention to detailDocumentation accuracyGood Manufacturing PracticesSOPsFDA regulationsWritten and verbal communicationOrganization

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Read the full posting here
BRAVO SHIFT: TUESDAY - FRIDAY 3:30PM - 2:00AM Pay: $21.49/Hourly with 15% Shift Differential 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 An associate's or bachelor's degree in a related field may be substituted for the required one (1) year of experience Clearance of favorable background investigation required

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