Facilities Commissioning & Qualification Expert

TechDigital Group; New Jersey; On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a skilled professional to oversee the commissioning and qualification of facilities and utilities within a dynamic environment. This role involves collaborating with diverse teams to ensure compliance with regulatory standards while providing exceptional customer service. The ideal candidate will possess a strong background in pharmaceutical manufacturing and utilities, demonstrating expertise in clean room environments and technical documentation. Join a forward-thinking organization that values innovation and teamwork, where your contributions will directly impact the success of critical projects in the pharmaceutical sector.

Qualifications

• 3+ years in FDA-regulated industry with experience in facility qualification.
• Strong background in laboratory and manufacturing operations.

Responsibilities

• Administer change control activities and corrective actions.
• Ensure timely completion of equipment commissioning projects.
• Maintain compliance with GMP and other standards.

Skills

cGMP knowledge

pharmaceutical manufacturing knowledge

commissioning and qualification of clean manufacturing facilities

scheduling and execution fundamentals

strong written and verbal communication skills

interpersonal skills

multi-tasking ability

Microsoft Office Suite proficiency

scheduling software knowledge

ability to create and analyze metrics

Education

BS in Engineering

Tools

scheduling software

inventory management systems

calibration management systems

environmental monitoring systems

Job description

An established industry player is seeking a skilled professional to oversee the commissioning and qualification of facilities and utilities within a dynamic environment. This role involves collaborating with diverse teams to ensure compliance with regulatory standards while providing exceptional customer service. The ideal candidate will possess a strong background in pharmaceutical manufacturing and utilities, demonstrating expertise in clean room environments and technical documentation. Join a forward-thinking organization that values innovation and teamwork, where your contributions will directly impact the success of critical projects in the pharmaceutical sector.