C&Q Specialist Packaging Automation

Validation & Engineering Group Inc.

• $80K — $95K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • At least 5 years of relevant C&Q experience in a pharmaceutical or biopharmaceutical environment.
  • Hands-on experience with packaging equipment and automated controls, including PLC/HMI systems.
  • Experience with FAT, SAT, IQ, OQ, and related qualification activities.
  • Strong technical writing skills.
  • Proven troubleshooting and cross-functional communication abilities.

Responsibilities

  • Develop, review, and execute commissioning and qualification protocols for packaging equipment and automation systems.
  • Support equipment startup, functional testing, and troubleshooting activities.
  • Review system requirements, drawings, specifications, and test results to ensure equipment performance.
  • Document test results, investigate discrepancies, and assist in their resolution.
  • Maintain clear and complete documentation in compliance with GMP requirements.

Benefits

  • Opportunity to work in a biopharmaceutical environment.
  • Collaboration with cross-functional teams including Engineering, Automation, and Quality.
  • Engagement in hands-on troubleshooting and problem-solving.
  • Involvement in critical qualification activities that impact product quality.
Full Job Description
We are seeking a C&Q Specialist - Packaging Automatio to support packaging equipment and automation systems in a biopharmaceutical environment. This role will work with Engineering, Automation, Operations, and Quality to bring systems into service and complete qualification activities.
  • C&Q Specialist • Packaging Automation

Description:
  • Develop, review, and execute commissioning and qualification protocols for packaging equipment and associated automation systems.
  • Support equipment startup, functional testing, and troubleshooting.
  • Review system requirements, drawings, specifications, and test results to confirm that equipment performs as intended.
  • Document test results, investigate discrepancies, and support their resolution.
  • Maintain clear, complete documentation in accordance with GMP requirements.

Qualifications:
  • At least 5 years of relevant C&Q experience in a pharmaceutical or biopharmaceutical environment.
  • Hands-on experience with packaging equipment and automated controls, including PLC/HMI systems.
  • Experience with FAT, SAT, IQ, OQ, and related qualification activities.
  • Strong technical writing, troubleshooting, and cross-functional communication skills.

#LI-LN1

#LI-ONSITE

Similar Jobs

More Jobs at Validation & Engineering Group Inc.

More Pharmaceuticals & Biotech Jobs

Find similar C&Q Specialist Packaging Automation jobs: