QC Supervisor- Environmental Monitoring/Metrology

Job Title: QC Supervisor Environmental Monitoring & MetrologyJob Description

The QC Supervisor Environmental Monitoring & Metrology leads and supports the Environmental Monitoring, Cleaning Validation, and Metrology teams within a modern, growing quality control laboratory. This role oversees critical activities such as environmental monitoring, cleaning verification and validation, and equipment calibration, ensuring compliance with cGMP requirements and alignment with production priorities. The supervisor collaborates closely with cross-functional teams, drives investigations and continuous improvement, and mentors a team of chemists in a fast-paced, dynamic environment.

Responsibilities

• Lead and support the Environmental Monitoring, Cleaning Validation, and Metrology teams to ensure all activities meet quality and regulatory expectations.
• Prioritize daily work based on Production needs, especially when manufacturing is waiting on cleaning verification or environmental testing results.
• Oversee environmental monitoring activities, including sampling, testing, data trending, and investigations related to environmental monitoring failures.
• Manage cleaning verification and cleaning validation to ensure manufacturing equipment and suites consistently meet established cleaning requirements.
• Coordinate cleaning activities with Production, Formulations, QC, and QA, ensuring timely resolution of issues and alignment with manufacturing schedules.
• Take a big-picture view when issues arise to confirm that cleaning requirements and procedures are followed and effectively implemented.
• Lead or support investigations related to environmental monitoring, cleaning, equipment, or calibration issues, and drive corrective and preventive actions.
• Oversee equipment calibration, preventive maintenance, and qualification activities to maintain compliance and reliable instrument performance.
• Help troubleshoot laboratory equipment and support teams in resolving technical issues with instruments such as HPLC, GC, and dissolution systems.
• Review and approve SOPs, protocols, reports, and other documentation related to Environmental Monitoring, Cleaning Validation, and Metrology.
• Participate in client and regulatory audits, providing subject matter expertise for environmental monitoring, cleaning validation, and metrology processes.
• Mentor, train, and develop team members, supporting their technical growth and helping them adapt to changing priorities and production demands.
• Promote a collaborative team environment, encouraging open communication and continuous learning across QC and related departments.
• Ensure all work complies with cGMP standards, internal procedures, and applicable regulatory requirements.
• Effectively manage time, resources, and schedules to balance multiple projects and shifting priorities.

Essential Skills

• B.S. degree in chemistry, biochemistry, biology, or a related life science field.
• At least 3 years of cGMP experience in a laboratory or pharmaceutical/biotech manufacturing environment.
• Experience in environmental monitoring and/or cleaning validation in a regulated setting (strongly preferred).
• Leadership experience supervising employees or leading teams, projects, or process improvement initiatives.
• Hands-on experience with analytical chemistry techniques such as HPLC, GC, titration, and wet chemistry.
• Strong background in quality control and QC testing within a cGMP framework.
• Experience in metrology, equipment qualification, or calibration (preferred).
• Familiarity with laboratory equipment operation and basic troubleshooting, including systems such as HPLC, GC, and dissolution instruments.
• Experience with systems such as Empower, LIMS, or MasterControl (helpful).
• Strong organizational and time-management skills with the ability to handle changing priorities.
• Proactive, self-motivated approach with a strong sense of urgency and ownership.
• Ability to see the bigger picture, ask thoughtful questions, and drive issues to resolution.
• Strong communication skills with the ability to work effectively with Production, QA, QC, and other cross-functional teams.
• Approachable and patient leadership style with the ability to support, coach, and motivate team members.

Additional Skills & Qualifications

• Experience leading cleaning validation projects and cleaning verification activities in a cGMP environment.
• background in analytical development or method development is beneficial.
• Demonstrated ability to lead investigations and implement corrective and preventive actions.
• Experience working in a multi-team QC structure (e.g., Raw Materials, Finished Products, Analytical Development, Environmental Monitoring).
• Ability to lead or support process improvements that enhance efficiency, data integrity, and compliance.
• Comfort working in a fast-paced environment where priorities can shift based on production needs.

Work Environment

This position is based in a quality control laboratory environment with dedicated Environmental Monitoring and Metrology teams consisting of approximately six chemists. The role backfills a team member who has been promoted to a manager-level position, reflecting strong internal growth opportunities. On the chemistry side, the QC lab is organized into four teamsRaw Materials, Finished Products, Analytical Development, and Environmental Monitoring/QC Specialistseach typically led by a supervisor overseeing around six chemists. The laboratory has expanded over the last two years and has been recently remodeled, offering a modern, clean, and collaborative workspace. Chemists work at shared workstations rather than individual desks, fostering a team-oriented environment, while scientist-level staff have dedicated desks. All chemists are equipped with laptops and work with a variety of analytical instruments, including HPLC, GC, dissolution systems, and other QC equipment. The work is varied, providing exposure to multiple techniques and instruments and encouraging ongoing learning and development. The role is full-time, with a standard laboratory schedule aligned to production and QC needs. The organization offers a competitive benefits package that includes a sign-on bonus, paid holidays (including New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving Day and the day after, Christmas Eve, and Christmas Day), and a robust paid time off program. Full-time employees accrue up to 17 days (136 hours) of PTO in their first year and 22 days (176 hours) per year after the first 12 months, with rollover allowed subject to a maximum accrual based on years of service. Accrued PTO can be used immediately, with supervisor approval, for both contract and permanent employees. The culture emphasizes teamwork, professional growth, and continuous learning in a modern laboratory setting.

Job Type & Location

This is a Permanent position based out of Verona, WI.

Pay and Benefits

The pay range for this position is $65000.00 - $85000.00/yr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Competitive Benefits Include: $0 monthly premium for medical insurance $0 monthly premium option for dental insurance Friendly work environment Medical, dental, vision, life, AD&D, and disability insurance Pre-tax 401(k) and after-tax Roth 401(k) contribution options with company matching up to 5% Generous paid time off, accruing up to 17 days of PTO within your first year Tuition reimbursement program Sign-on bonus

Job Type & Location

This is a Permanent position based out of Verona, WI.

Application Deadline

This position is anticipated to close on Nov 16, 2026.

Workplace Type

This is a fully onsite position in Verona,WI.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.