CIP Shakedown Night-Shift Lead (Onsite)

Piper Companies

Holly Springs (NC)

On-site

USD 83,000 - 103,000

Full time

14 days+
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Benefits offered by this job

Medical

Job summary

Piper Companies is seeking a CIP Shakedown Shift Lead for a fully onsite contract in Holly Springs, NC. You will provide hands-on leadership during facility startup, supporting CIP readiness and guiding production personnel on a rotating 12-hour night schedule as operations move into commercial manufacturing.

Responsibilities include leading shakedown activities, troubleshooting, and collaborating with engineering, maintenance, validation, and manufacturing to ensure system reliability and GMP

Qualifications

  • Leadership experience in manufacturing, pharmaceutical, biotechnology, or industrial production.
  • Startup/shakedown experience supporting manufacturing processes or equipment.
  • Strong troubleshooting and root cause investigation skills in a fast-paced setting.
  • Knowledge of GMP regulations, safety requirements, and SOPs.
  • Ability to lead teams and collaborate with cross-functional groups during startup activities.

Responsibilities

  • Lead startup, shakedown, and readiness activities for CIP systems and equipment.
  • Direct operators and technicians on a rotating 12-hour night shift.
  • Troubleshoot equipment, process, and operational issues during startup and early production.
  • Partner with engineering, maintenance, validation, and manufacturing teams to drive reliability.
  • Promote GMP compliance and continuous improvement across operations.

Skills

Leadership
Troubleshooting
GMP knowledge
Shift leadership
Cross-functional teamwork

Job description

Piper Companies is seeking a CIP Shakedown Shift Lead for a fully onsite contract in Holly Springs, NC. You will provide hands-on leadership during facility startup, supporting CIP readiness and guiding production personnel on a rotating 12-hour night schedule as operations move into commercial manufacturing.

Responsibilities include leading shakedown activities, troubleshooting, and collaborating with engineering, maintenance, validation, and manufacturing to ensure system reliability and GMP

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