Core Technician - Day Shift

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

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.

• 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.

• 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.

• 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.