Sterile Packaging & Cleanroom Lead

Acero Precision Inc

West Chester, PA

JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Cleanroom, Coaching, Code of Federal Regulations, Detail Oriented, Documentation, Employee Assistance Plan, Engineering Drawing, Environmental Monitoring, FDA (Food and Drug Administration), Health Insurance, Healthcare Quality, High School Diploma, ISO (International Organization for Standardization), Internal Audit, Leadership, Maintain Compliance, Manufacturing, Medical Equipment, Patient Care, Preventative Maintenance, Process Improvement, Process Validation, Product Testing, Quality Metrics, Regulations, Sterilization, System Validation, Team Player, Writing Skills
LOCATION
West Chester, PA
POSTED
7 days ago

Cleanroom Operations & Sterile Packaging Technician

Location: West Chester, PA

Industry: Medical Device Manufacturing

Help Build Medical Devices That Improve Lives

Are you passionate about quality, precision, and working in a highly regulated manufacturing environment? Join our team as a Cleanroom Operations & Sterile Packaging Technician, where youll 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 Youll Do

As a member of our Cleanroom Operations team, you will:

  • 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 Were Looking For

Required Qualifications

  • High school diploma or equivalent with 5+ years of leadership or hands-on experience in a cleanroom environment, OR
  • Bachelors 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 Youll 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 youre someone who values precision, quality, and making a meaningful impact through your work, wed love to hear from you. Apply today and help us deliver innovative medical devices that make a difference.

Acero Precision is proud to be an Equal Opportunity Employer. Acero Precision does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need.

  • Principals only. Recruiters please do not apply on behalf of your candidates to Acero Precision job posts. All applications and/or contact information submitted are kept on file and are the property of Acero Precision. Please note recruiting fees will not be honored with candidate applications submitted by recruiters.

Make Our Mission Your Mission!

About the Company

A

Acero Precision Inc

Acero Precision is a ISO 13485 & ISO 9001, accredited, state-of-the-art manufacturing facility. Just having recently celebrated its 30th year of operation, Acero Precision has evolved into an industry leading original equipment manufacturer (OEM) with the ability to serve clients around the world. We are proud of our elite team of talented engineers, CNC programmers, machinists, and quality control inspectors, who are dedicated to producing the very best in precision engineered components every day. Acero Precision promotes the use of advanced technology to maintain a steady flow of manufacturing jobs in the US; an initiative that is a main cornerstone of Acero Precision’s culture.

COMPANY SIZE
50 to 99 employees
INDUSTRY
Medical Devices and Supplies
FOUNDED
1984
WEBSITE
http://aceroprecision.com/