Aseptic Technician

CareerCircle
Summit, NJ, United States
2 days ago
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Role details

Contract type
Temporary to permanent
Employment type
Full-time (> 32 hours)
Experience level
Starter
Experience required
1 year minimum
Compensation
$47,840.0 - $49,920.0
Working hours
Shift work

Tech stack

Active Directory Apple IOS Microsoft Azure Command-Line Interface Computer Literacy Disaster Recovery Experimental Data Identity and Access Management Python (Programming Language) Linux System Administration Linux Servers Windows Servers
+11 more
Operational Databases Windows PowerShell Data Logging Electronic Filing System Load Balancing Azure Powershell Infrastructure as Code (IaC) Git Tanium Platform Expertise Patch Management Software Version Control

Job description

The Aseptic Technician plays a key role in supporting sterilization operations within ISO 6 and ISO 7 cleanroom environments. This position focuses on washing glassware and medical components, performing aseptic cleaning and sterilization tasks, maintaining aseptic samples, and monitoring process systems and equipment to ensure proper operation. The role requires adherence to GMP and SOP guidelines, accurate documentation, and active participation in safety and quality practices on a consistent basis., * Wash glassware and medical components using designated equipment in accordance with established procedures.

  • Work in ISO 6 and ISO 7 cleanroom environments while wearing all required personal protective equipment (PPE).
  • Perform aseptic cleaning and sterilization activities to support pharmaceutical, medical device, and biotech operations.
  • Maintain aseptic samples and ensure they are handled and stored according to GMP and SOP requirements.
  • Monitor process systems and equipment to verify proper operation and promptly report any deviations.
  • Perform daily and weekly preventative maintenance tasks on equipment and assist the maintenance team as needed.
  • Participate in safety committees and strictly adhere to all safety rules, procedures, and regulations.
  • Accurately complete all required documentation, including batch records, reviews, and other GMP-related forms.
  • Clean, sanitize, and disinfect workstations before and after use to maintain a sterile and orderly environment.
  • Demonstrate strong attention to detail and maintain high accuracy in all work performed.
  • Perform additional tasks as assigned by the supervisor to support ongoing operations and projects.
  • Adapt to different processes and workflows depending on the project requirements., Azure DevOps Linux Servers Microsoft Azure Server Patching Active Directory Patch Management Disaster Recovery Windows PowerShell Business Valuation Azure Load Balancer Linux Administration Backup Administration Full Stack Development Business Transformation Git (Version Control System) Infrastructure as Code (IaC) Python (Programming Language) ITIL Foundation Certification Identity And Access Management Tanium (Endpoint Management Software) Microsoft Windows Server Administration Azure Command-Line Interface (Azure CLI) +0 Login | JoinContact

Requirements

Visionary Operations Innovation Punctuality Disinfecting Biotechnology Sterilization Pharmaceuticals Detail Oriented Medical Devices Computer Literacy Strong Work Ethic Aseptic Processing Sterile Processing Workflow Management Process Architecture Engineering Design Process Standard Operating Procedure Good Manufacturing Practices, * 1-2 years of industry experience in aseptic processing, sterile processing, pharmaceutical, or related GMP environments is ideal.

  • Hands-on experience working in cleanroom or laboratory environments with aseptic techniques.
  • Strong knowledge of GMP principles and the ability to follow SOPs consistently.
  • Experience with aseptic cleaning, sterilization, and aseptic technique in operational settings.
  • Ability to handle, review, and maintain batch records in alignment with good documentation practices.
  • Basic computer skills to work within internal databases and electronic documentation systems.
  • Proven punctuality, flexibility, and strong work ethic in a production or laboratory environment.
  • Ability to wear required PPE and gown for extended periods while maintaining compliance with cleanroom protocols., * Experience in pharmaceutical, compound pharmacy, medical device, biotech, or related GMP industry.
  • Experience in cleanroom operations and sterile processing environments.
  • Familiarity with operation of sterilization equipment and process systems.
  • Commitment to long-term growth and development within the organization.
  • Strong attention to detail and accuracy in both technical tasks and documentation.
  • Comfort working with a home-grown internal database and learning new systems.
  • Ability to collaborate effectively with safety committees and cross-functional teams., 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., Dayton, NJ*On-Site

Dosing Biology Asepsis Research Visionary Scheduling Mentorship Innovation Microscopy Toxicology Mycoplasma Morphology Cell Growth Disassembler Cell Biology Life Sciences Cell Cultures Animal Models Data Recording Detail Oriented Time Management Medical Devices Experimental Data Laboratory Safety Molecular Biology Chemical Kinetics Population Health Biochemical Assays Sample Preparation Bacterial Cultures Suspension (Vehicle) Laboratory Equipment Management Of Cancer Organizational Skills Laboratory Procedures Laboratory Techniques Polymerase Chain Reaction Engineering Design Process Standard Operating Procedure Good Laboratory Practice (GLP)

Benefits & conditions

  • This role is based in ISO level 6 and 7 cleanroom environments focused on steam and dry heat sterilization for pharmaceutical, medical device, and biotech applications.
  • The position requires gowning and wearing full PPE for 6-10 hours at a time, with scheduled breaks provided during the shift.
  • The standard schedule is 2nd shift, Monday through Friday, from 2:00 p.m. to 10:30 p.m.
  • The facility emphasizes strict GMP compliance, SOP adherence, and robust safety practices.
  • The work setting offers lab expansion and growth potential, providing opportunities to develop skills and advance within a highly regulated and quality-driven environment.

Job Type & Location

This is a Contract to Hire position based out of Summit, NJ. Pay and Benefits

The pay range for this position is $23.00 - $24.00/hr.

About the company

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.

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