Central Services Technician, I (Temp to Perm)

Cellipont Bioservices•The Woodlands, TX

About The Position

Kincellis Advanced Therapies is a cell therapy contract development and manufacturing organization supporting the development and manufacturing of treatments for patients worldwide. The Central Services Technician I supports GMP manufacturing batch records, maintains necessary supply levels in manufacturing areas, and helps support the overall GMP manufacturing process. The role performs facility cleaning, material kitting, and material transfers, with an emphasis on accurate, proactive execution. It documents activities to meet cGMP requirements and uses central services processing equipment according to established SOPs. The position also contributes to continuous improvement and cost-savings efforts, complies with regulatory and quality requirements, and reviews daily GMP documentation for accuracy and completeness.

Requirements

  • High school diploma or GED.
  • Strong communication skills.
  • Ability to lift at least 25 pounds.
  • Basic computer skills, including Microsoft Office.
  • Ability to work in a lean, action-oriented organization and demonstrate a strong work ethic.
  • Flexibility, adaptability, self-motivation, and the ability to work independently and cross-functionally with teams.

Nice To Haves

  • One to two years of experience working in a GMP facility; reduced experience may be considered with increased education in an applicable discipline.

Responsibilities

  • Execute facility cleaning, material kitting, and material transfers on a day-to-day basis, emphasizing right-first-time execution.
  • Document activities to meet cGMP requirements.
  • Operate central services processing equipment according to established SOPs, including cleaning systems, biological safety cabinets, mixers, autoclaves, washers, and balances or scales.
  • Help identify and support continuous improvement opportunities and identify waste within work processes.
  • Identify cost-savings projects or initiatives.
  • Adhere to cGMPs, compliance and regulatory mandates, and quality requirements.
  • Review daily GMP documentation, including logbooks and batch records, for accuracy and completeness.
  • Perform other duties as assigned to meet departmental and company objectives.
  • Develop and maintain strong working relationships with primary support functions.

Benefits

  • Opportunities for career growth within an expanding team.
  • Cross-functional exposure to other areas within the organization.
  • Benefits package addressing health and wellness needs, including coverage for pets at select site locations.
  • 401(k) employer match.
  • Tuition reimbursement, based on departmental budget and role-specific qualifications.
  • Employee referral bonuses.
  • A workplace that values diversity, inclusion, and organizational culture.
  • Flexible work schedules for eligible roles.
  • Paid time off and paid holidays.
  • Opportunity to build expertise in the cell therapy field.
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