QC Env Monitoring Lead: Metrology & Cleaning Validation

COATING PLACE LLC; Verona (WI); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Sign-on bonus

Job summary

Coating Place is seeking a QC Supervisor for Environmental Monitoring, Cleaning Validation, and Metrology in Verona, WI. You will lead EM, Cleaning Validation, and Metrology programs, ensuring compliance with cGMP, USP, ICH and FDA guidelines, and providing technical oversight.

The role requires supervision experience in pharma or related cGMP settings, strong leadership, and collaboration with Production, QC, and QA teams. On-site responsibilities include audits and ensuring program integrity.

Qualifications

• Bachelor's degree in microbiology, chemistry, or related field.
• 3+ years of supervisory experience in a pharmaceutical environment or 5+ years at Coating Place, Inc.
• Thorough knowledge of analytical and microbiological equipment; understanding of USP/ICH/FDA guidelines.

Responsibilities

• Supervises EM, Cleaning Validation, and Metrology personnel; assigns work and evaluates performance.
• Coordinates resources, communicates status and issues to stakeholders.
• Prioritizes cleaning verification activities and minimizes production interruptions.
• Oversees calibration, maintenance, and qualification of laboratory equipment.
• Drafts and approves SOPs, protocols, trend reports and technical docs.
• Participates in on-site client and regulatory audits.
• Maintains knowledge of relevant regulatory requirements and best practices.
• Follows GMP practices and safety procedures.

Skills

Leadership

Time management

Communication

Teamwork

Problem solving

Education

Bachelor's degree in microbiology/related field

Supervisor experience in pharma or 5+ years at Coating Place

Job description

Coating Place is seeking a QC Supervisor for Environmental Monitoring, Cleaning Validation, and Metrology in Verona, WI. You will lead EM, Cleaning Validation, and Metrology programs, ensuring compliance with cGMP, USP, ICH and FDA guidelines, and providing technical oversight.

The role requires supervision experience in pharma or related cGMP settings, strong leadership, and collaboration with Production, QC, and QA teams. On-site responsibilities include audits and ensuring program integrity.