Job Title:
Aseptic Technician - 2nd Shift Job Description This role focuses on performing aseptic cleaning, sterilization, and packaging activities in an ISO-6 and ISO-7 cleanroom environment in support of pharmaceutical, medical device, and biotech operations. The aseptic technician follows Good Manufacturing Practices (GMP), adheres to standard operating procedures (SOPs), and maintains high standards of cleanliness, documentation, and safety while handling glassware, medical components, and aseptic samples. This position offers growth potential within an expanding laboratory environment for individuals who are punctual, flexible, hardworking, and interested in long-term development. Responsibilities Wash glassware and medical components using designated equipment and procedures to ensure they meet cleanliness and sterility requirements. Work consistently in ISO-6 and ISO-7 cleanroom environments while wearing the required personal protective equipment (PPE). Perform aseptic cleaning and packaging of products, strictly following aseptic techniques to prevent contamination. Maintain aseptic samples by handling, storing, and documenting them according to established GMP and SOP requirements. Monitor process systems and equipment to verify proper operation and promptly report or address any deviations. Perform daily and weekly preventative maintenance tasks on assigned equipment and assist the maintenance team as needed. Participate actively in safety committees and follow all safety rules, guidelines, and regulations. Accurately complete all required documentation for each task, including logs, forms, and electronic records, following good documentation practices. Clean, sanitize, and disinfect workstations before and after use to maintain a controlled and compliant environment. Demonstrate strong attention to detail and maintain high work accuracy in all aseptic and documentation tasks. Perform additional tasks and special assignments as directed by the supervisor to support ongoing operations. Adapt to different processes and workflows based on the specific client or project requirements assigned. Essential Skills Proven experience working with aseptic techniques and sterile processing in a laboratory, pharmaceutical, or cleanroom setting. Industry experience of 1-2 years in a GMP or pharmaceutical environment is ideal. Hands-on experience working in cleanroom environments, preferably ISO-6 and ISO-7 classifications. Knowledge and practical understanding of Good Manufacturing Practices (GMP) and the ability to follow standard operating procedures (SOPs). Good documentation practices, including accurate, legible, and compliant recordkeeping. Basic computer skills to navigate and use an internal, home-grown database or electronic systems. Experience with sterilization processes such as steam and dry heat sterilization or related sterile operations. Ability to monitor and operate process systems and equipment safely and effectively. Strong attention to detail, high accuracy in work, and a commitment to quality. Punctuality, flexibility, and a strong work ethic, with an interest in long-term employment and growth. Additional Skills & Qualifications Background in pharmaceutical, GMP, or related regulated industry environments. Experience in laboratory operations, including handling glassware, medical components, and aseptic samples. Familiarity with aseptic techniques, cleanroom behavior, and contamination control practices. Understanding of sterile processing workflows and requirements in pharmaceutical or medical device settings. Ability to collaborate with safety committees and cross-functional teams. Interest in professional development and advancement within a growing laboratory operation. Comfort working with internal databases and adapting to new systems or technologies. Work Environment The role is based in ISO-6 and ISO-7 cleanroom environments that support contract steam and dry heat sterilization services for pharmaceutical, compound pharmacy, medical device, and biotech industries. Aseptic technicians work fully gowned for extended periods, typically 6-10 hours at a time, with scheduled breaks to support comfort and safety. The position operates on a 2nd shift schedule, Monday through Friday, from 2:00 p.m. to 10:30 p.m. The facility emphasizes strict adherence to GMP, SOPs, and safety protocols, and provides opportunities for growth within an expanding laboratory, including lab expansion initiatives and internal advancement opportunities. The work involves regular use of sterilization equipment, cleanroom tools, and computer systems to manage documentation and internal databases in a structured, process-driven environment. Job Type & Location This is a Contract to Hire position based out of Fairfield, NJ. Pay and Benefits The pay range for this position is $23.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fairfield,NJ.
Application Deadline This position is anticipated to close on Jun 16, 2026. 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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.