Calibration Technician

The Calibration Technician performs hands-on calibration, maintenance, and troubleshooting of complex manufacturing and utility systems in a highly regulated pharmaceutical environment. This role ensures that critical equipment operates within defined specifications, supports facility start-up and commissioning activities, and maintains accurate documentation in compliance with cGMP and Good Documentation Practices. The technician provides technical support to internal customers, responds to high-priority work requests, and actively promotes a safe and compliant work environment.

• Perform calibrations on manufacturing and utility systems, including Building Automation and Controls and Rockwell PLCs, to ensure equipment operates within required specifications.
• Operate, troubleshoot, and repair complex utility systems such as WFI, RODI, Clean Steam, CIP, autoclaves, glassware washers, production vessels, HVAC systems, cold and warm rooms, control systems, compressed gases, plant steam and condensate, bulk chemical distribution, and wastewater treatment systems.
• Provide technical direction and responsive customer support to operations and other internal stakeholders, ensuring timely resolution of technical issues.
• Assist with facility start-up projects by performing initial calibrations and commissioning activities as required to bring systems into validated operation.
• Complete and maintain accurate documentation for all calibration, maintenance, and repair activities in cGMP operations, following Good Documentation Practices and EAM policies and procedures.
• Review and close all preventive and corrective maintenance records in a timely manner, ensuring completeness, accuracy, and compliance with established procedures.
• Respond to emergency and high-priority work requests, assign tasks as needed, and ensure that all work is completed safely, effectively, and in compliance with applicable policies.
• Ensure all activities comply with safe work practices and site policies, including lockout/tagout and other safety procedures, as applicable.
• Promote a safe working environment by supporting site Health, Safety, and Environment (HSE) policies and programs.
• Ensure compliance with local HSE regulations, complete required HSE trainings, and consistently follow safety procedures.
• Report accidents, incidents, and near misses, support investigations, and ensure timely closure of HSE-related corrective and preventive actions.

• Minimum of 5 years of experience in a hands-on calibration or metrology technician role.
• Experience working in a pharmaceutical manufacturing environment.
• Strong electronics and electrical troubleshooting experience.
• Proficiency in performing calibrations on manufacturing and utility systems, including Building Automation and Controls and Rockwell PLCs.
• Ability to operate, troubleshoot, and repair complex utility systems such as WFI, RODI, Clean Steam, CIP, autoclaves, glassware washers, production vessels, HVAC, cold and warm rooms, compressed gases, plant steam and condensate, bulk chemical distribution, and wastewater treatment systems.
• Experience working in regulated environments with cGMP requirements.
• Ability to complete accurate and compliant documentation following Good Documentation Practices and EAM policies and procedures.
• Strong understanding of safe work practices and HSE principles.
• Effective communication skills for providing technical direction and responsive customer support.
• Ability to respond to and manage emergency and high-priority work requests in a structured and timely manner.

• Aseptic gowning experience is a plus.
• Experience in large-scale, highly regulated pharmaceutical or life sciences environments.
• Familiarity with commissioning activities and facility start-up projects.
• Exposure to best practices in pharmaceutical services and contract development and manufacturing (CDMO) environments.

This is an onsite role in a large-scale, highly regulated pharmaceutical manufacturing environment that emphasizes safety, quality, and compliance. The position initially follows a schedule of approximately 7:00 a.m. to 4:00 p.m. for the first few months to allow for onboarding and acclimation. Once acclimated, the regular shift transitions to approximately 12:00 p.m. to 8:00 p.m., with the potential to move to a third shift if the facility becomes fully 24/7 operational. The work involves frequent interaction with complex utility and manufacturing systems, including automation and control technologies, and requires consistent adherence to cGMP, Good Documentation Practices, and HSE policies. The environment offers exposure to advanced pharmaceutical manufacturing practices, large-scale systems, and structured processes typical of a global leader in pharma services and life sciences.

This is a Contract to Hire position based out of Ridgefield, NJ.

The pay range for this position is $40.00 - $50.00/hr.

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.

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)

This is a fully onsite position in Ridgefield,NJ.

This position is anticipated to close on Oct 19, 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 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 View email address on click.appcast.io 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.