Job Title: Core Technician I
Location: 14905 Kirby Drive Houston, TX 77047
Shift: Day Shift – 7:00 AM to 7:30 PM (12-hour rotating schedule: 2 days on, 2 days off, 3 days on, 3 days off)
Duration: 6-month contract with potential for extension or conversion
Pay Rate: $25.00 per hour
Job Summary:
The Core Technician I is responsible for supporting the production of sterile biological pharmaceutical products within a cGMP-regulated manufacturing environment. This position performs production-related activities in cleanroom settings, follows established procedures and quality systems, and ensures compliance with safety and regulatory requirements.
Responsibilities:
• Perform production activities associated with the manufacture of sterile biological pharmaceutical products.
• Follow written procedures, work instructions, and established guidelines to complete assigned tasks accurately.
• Recognize and report deviations from accepted practices, procedures, or quality standards.
• Support and maintain cGMP compliance by adhering to company processes, procedures, and documentation requirements.
• Comply with all safety policies, procedures, and regulatory requirements.
• Work collaboratively with team members to maintain a safe and compliant manufacturing environment.
• Support quality systems and ensure all activities are performed in accordance with regulatory requirements.
• Assist in maintaining a positive work environment that promotes teamwork, communication, and continuous improvement.
• Prioritize multiple tasks and responsibilities while supporting production schedules and operational goals.
Work Environment:
• Majority of work is performed in a cleanroom environment.
• Full cleanroom gowning is required, including scrubs, hairnet, shoe covers, hood, gown, mask, boots, and double gloves.
Qualifications:
• Bachelor's Degree in Life Sciences preferred.
• Basic laboratory experience with a Bachelor's Degree OR intermediate laboratory experience in a cGMP clinical production environment with a High School Diploma.
• Laboratory experience preferred.
• 1–3 years of relevant experience.
• Experience working in a regulated manufacturing, biotechnology, pharmaceutical, or laboratory environment is preferred.
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Tailored Management is a global staffing firm that specializes in partnering with large organizations that run their contingent labor program in a VMS/MSP environment. We have the unique capacity to support programs across all scopes and geographic locations from a single headquarters, successfully elevating program performance across the board and minimizing costs, miscommunication and delivery times. But what do we really do? We bring together the best talent with the greatest opportunities.