QC Contractor PM

Quanta Consultancy Services Ltd; Kentucky; On-site; USD 80,000 - 100,000; Full time

Job summary

Quanta Consultancy Services Ltd is seeking a QC Contractor PM for a major pharmaceutical project in Ohio, enhancing the future of medicine manufacturing. The selected candidate will coordinate activities across testing sites and manage documentation to support a multi-billion-dollar facility.

A degree in Engineering or a related technical field, along with QC laboratory experience in a cGMP environment, is essential. Join this extraordinary project and help shape the future of pharmaceuticals!

Qualifications

• Minimum Engineering or related technical degree required.
• Experience in pharmaceutical manufacturing is essential.
• Project management skills with timelines and deliverables are expected.

Responsibilities

• Coordinate sample lifecycle activities with testing sites.
• Track sample status, testing progress, and turnaround times.
• Manage QC documentation lifecycle including testing protocols.

Skills

QC laboratory experience in cGMP environment

Project management experience

Strong understanding of data integrity (ALCOA)

Education

Engineering or Science degree

Job description

QC Contractor PM – Master Data - US, Ohio - 12 Month Contract. Be part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Ohio, a multi-billion-dollar investment designed to push the boundaries of science and engineering. We’re looking for a QC Contractor PM to join the team and help deliver this world-class program.

What you’ll do:

• Coordinate sample lifecycle activities with internal/external testing sites
• Track sample status, testing progress, turnaround times
• Track and support laboratory investigations from initiation to closure
• Maintain investigation logs and status updates
• Manage QC documentation lifecycle (CCs, COAs/COTs, testing protocols)

What you’ll need:

• Engineering or Science degree preferred (minimum: Engineering or related technical degree)
• QC laboratory experience in cGMP environment
• Experience in pharmaceutical manufacturing
• Strong understanding of data integrity (ALCOA)
• Proven project management experience with timelines & deliverables

Don’t miss your chance to be part of something extraordinary, apply now and let’s talk!