Core Technician I

SGS Consulting; Clifton (TX); On-site; USD 38,000 - 52,000; Full time

Job summary

SGS Consulting is seeking a detail-oriented laboratory technician to support sterile production in a cGMP environment in Texas. The role focuses on following SOPs and work instructions with high accuracy while ensuring safety and regulatory compliance.

The position requires 1–3 years in a lab or cGMP setting, a Life Sciences degree or equivalent experience, and the ability to work rotating 12-hour shifts in a cleanroom with full PPE.

Qualifications

• Experience in laboratory or cGMP manufacturing preferred.
• Bachelor's degree in Life Sciences preferred or equivalent lab experience with high school diploma.
• Experience in cleanroom or sterile production environments is a plus.
• Strong understanding of SOP-driven environments and regulatory compliance.
• Ability to follow detailed written instructions precisely.
• Strong attention to detail and quality mindset.

Responsibilities

• Perform tasks related to production of sterile biological pharmaceutical products in a cGMP environment
• Follow written procedures, SOPs, and work instructions with high accuracy
• Ensure compliance with all safety policies, quality standards, and regulatory requirements
• Work in a cleanroom environment requiring full PPE including gowning, gloves, mask, and hood
• Identify and report deviations from established procedures or accepted practices
• Support maintenance of quality systems and manufacturing compliance standards
• Collaborate with team members to ensure smooth production operations
• Assist in maintaining cleanroom integrity and contamination control practices
• Support training and onboarding activities during initial training period
• Help ensure smooth shift operations in a rotating 12-hour schedule
• Maintain documentation and production records accurately

Skills

1-3 years exp

Attention to detail

Teamwork

Follow SOPs

Regulatory compliance

Education

Bachelor's degree in Life Sciences

High School Diploma with relevant lab experience

Job description

Job Responsibilities:

• Perform tasks related to production of sterile biological pharmaceutical products in a cGMP environment
• Follow written procedures, SOPs, and work instructions with high accuracy
• Ensure compliance with all safety policies, quality standards, and regulatory requirements
• Work in a cleanroom environment requiring full PPE including gowning, gloves, mask, and hood
• Identify and report deviations from established procedures or accepted practices
• Support maintenance of quality systems and manufacturing compliance standards
• Collaborate with team members to ensure smooth production operations
• Assist in maintaining cleanroom integrity and contamination control practices
• Support training and onboarding activities during initial training period
• Help ensure smooth shift operations in a rotating 12-hour schedule
• Maintain documentation and production records accurately

Skills:

• 1-3 years of laboratory or cGMP manufacturing experience preferred
• Bachelor's degree in Life Sciences preferred or equivalent lab experience with high school diploma
• Experience working in cleanroom or sterile production environments is a plus
• Strong understanding of SOP-driven environments and regulatory compliance
• Ability to follow detailed written instructions precisely
• Strong attention to detail and quality mindset
• Basic understanding of biological or pharmaceutical manufacturing processes
• Ability to work in rotating shifts and extended training schedules
• Strong teamwork, communication, and reliability in production settings

Education/Experience:

• Bachelor's degree in Life Sciences preferred; High School Diploma with relevant lab experience acceptable