Central Services Technician, I (Temp to Perm)

Cellipont Bioservices•The Woodlands, TX

About The Position

Kincellis Advanced Therapies is seeking a Central Services Technician I to support GMP manufacturing of cell therapies. The role supports execution of GMP manufacturing batch records, maintains necessary supply levels in manufacturing areas, and contributes to the overall GMP manufacturing process by applying knowledge of relevant principles to operational and routine production tasks. Day-to-day work includes facility cleaning, material kitting and transfers, equipment operation according to established SOPs, and documentation and review of GMP activities. The technician also supports continuous improvement and cost-saving initiatives while adhering to cGMP, regulatory, compliance, and quality requirements.

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.
  • Flexible, adaptable, and self-motivated, with the ability to work independently and cross-functionally.
  • Ability to develop and maintain strong working relationships with primary support functions.

Nice To Haves

  • 1–2 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, with a focus on right-first-time execution.
  • Document all activities to meet cGMP requirements.
  • Use 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 implementation of continuous improvement opportunities and identify waste in work processes.
  • Identify cost-saving projects or initiatives.
  • Adhere to cGMPs, compliance and regulatory mandates, and quality requirements.
  • Review daily GMP documentation for accuracy and completeness, including logbooks and batch records.
  • Perform other duties as assigned to meet departmental and company objectives.

Benefits

  • Opportunities for career growth within an expanding team.
  • Cross-functional exposure to other areas within the organization.
  • Benefit package designed for 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.
  • Flexible work schedules where applicable to the role.
  • PTO and paid holidays.
  • Opportunity to build expertise in the cell therapy field.
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