Sterile Packaging & Cleanroom Supervisor

Acero Precision

$90K — $100K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of leadership or hands-on experience in a cleanroom environment, OR 2+ years with a bachelor's degree
  • Strong attention to detail and accuracy in documentation
  • Ability to follow written procedures in a controlled environment
  • Experience in regulated environments such as medical devices, pharmaceuticals, or biotechnology is preferred
  • Knowledge of ISO packaging standards and FDA regulations is a plus
  • Cleanroom operations or sterile processing certification is advantageous.

Responsibilities

  • Lead cleanroom operations from production to environmental monitoring
  • Perform final assembly of medical devices using engineering drawings
  • Conduct inspections to ensure product quality meets standards
  • Package products using validated cleaning processes and sterile barrier systems
  • Document quality activities and maintain product traceability
  • Support internal audits and compliance with quality requirements
  • Assist with process improvements and equipment qualifications.

Benefits

  • Work on life-changing medical devices that impact patient care
  • Collaborative team environment focused on quality and process improvement
  • State-of-the-art, climate-controlled manufacturing facility
  • Opportunities for professional growth and continued learning
  • Comprehensive health insurance plans and wellness programs
  • 401(k) plan with employer match
  • Generous PTO and paid holidays.
Full Job Description
Cleanroom Operations & Sterile Packaging Supervisor

Salary Range: $90,000 - $100,000 annually

Location: West Chester, PA
Industry: Medical Device Manufacturing

Are you passionate about quality, precision, and working in a highly regulated manufacturing environment? Join our team as a Cleanroom Operations & Sterile Packaging Supervisor, where you'll play a critical role in the final assembly, inspection, cleaning, and sterile barrier packaging of life-changing medical devices.

This position is ideal for someone with cleanroom experience who thrives in a detail-oriented environment and takes pride in producing products that directly impact patient care.

What You'll Do

As a member of our Cleanroom Operations team, you will:
  • Lead and perform all cleanroom activities from the bench up: hands-on production, ISO Class 7 requalification, calibration of supporting cleanroom equipment and systems, environmental monitoring, excursion investigation and documentation, and routine bioburden analysis for the sterile barrier system process.
  • Perform final assembly of medical devices following detailed work instructions and engineering drawings.
  • Clean and prepare medical devices using validated cleaning processes.
  • Conduct visual and dimensional inspections to ensure products meet strict quality standards.
  • Package products using validated sterile barrier systems, including pouches and trays.
  • Operate heat-sealing equipment and verify seal integrity.
  • Apply labels, lot numbers, expiration dates, and regulatory markings accurately.
  • Complete ERP transactions and maintain complete product traceability.
  • Document batch records, inspections, and quality activities.
  • Identify and report non-conforming products.
  • Monitor cleanroom environmental conditions and support routine preventive maintenance activities.
  • Assist with process improvements, equipment qualifications (IQ/OQ/PQ), validations, and new product/process transfers.
  • Support internal audits and maintain compliance with FDA and ISO quality requirements.

What We're Looking For
Required Qualifications
  • High school diploma or equivalent with 5+ years of leadership or hands-on experience in a cleanroom environment, OR
  • Bachelor's degree with 2+ years of related technical experience.
  • Strong attention to detail and documentation accuracy.
  • Ability to follow written procedures and work in a controlled cleanroom environment.

Preferred Qualifications
  • Experience in medical device, pharmaceutical, biotechnology, or another regulated manufacturing environment.
  • Previous sterile barrier packaging experience.
  • Knowledge of ISO 11607, ASTM packaging standards, or gamma sterilization processes.
  • Familiarity with FDA 21 CFR Part 820, ISO 13485, and ISO 14644.
  • Cleanroom operations or sterile processing certification is a plus.

Why Join Us?
  • Work on products that improve patients' lives around the world.
  • Be part of a growing, quality-focused medical device manufacturer.
  • Collaborative team environment with opportunities to support process improvements and validation projects.
  • Stable, clean, and professional manufacturing environment.
  • Opportunities for professional growth and continued learning.

Why You'll Love Working Here
  • Competitive compensation based on experience
  • Overtime opportunities available
  • State-of-the-art climate-controlled manufacturing facility
  • 100% paid uniforms
  • Multiple health insurance plans, including no-cost HAS options for eligible employees
  • Dental and vision coverage
  • 401 (k) with employer match
  • 100 hours of PTO during your first year
  • 7 paid holidays annually
  • Employee Assistance Program (EAP)
  • Wellness Coach Program access
  • Stable, long-term career opportunities within a growing medical device manufacturer

If you're someone who values precision, quality, and making a meaningful impact through your work, we'd love to hear from you. Apply today and help us deliver innovative medical devices that make a difference.

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