Manufacturing Technician
Actalent, Clayton, NC, United States
Manufacturing Technician
The Manufacturing Technician sets up, operates, monitors, and controls manufacturing equipment, systems, and processes in a regulated, cleanroom environment. This role supports the execution of the production schedule, ensures product quality and compliance with GMP standards, and contributes to a safe, efficient, and highly collaborative manufacturing operation.
Responsibilities
Set up, operate, monitor, and control manufacturing equipment, systems, and processes according to established procedures.
Clean and sanitize manufacturing, filling, and packaging rooms and equipment in accordance with standard operating procedures (SOPs).
Execute the production schedule to meet daily and long-term production goals.
Handle labeling and components accurately, including transferring, counting, applying FIFO (first-in, first-out) practices, and processing returns.
Actively participate in and support event response activities to address production or quality issues.
Review and author SOPs and other controlled documents as required to support continuous improvement and compliance.
Identify, report, and assist in resolving quality issues in a timely and compliant manner.
Execute and assist with equipment maintenance activities, including restoration of lost function, predictive maintenance, and preventative maintenance tasks.
Train fellow employees in areas of personal expertise and proactively learn new systems and equipment beyond current specialization.
Record and review production data in batch production records (BPR) and associated forms with a high degree of accuracy and completeness.
Follow all safety and environmental requirements while performing daily duties.
Perform other related accountabilities and tasks as assigned to support manufacturing operations.
Essential Skills
Previous experience working under GMP (Good Manufacturing Practice) or in a regulated manufacturing environment.
Experience in cleanroom operations and adherence to cleanroom protocols.
Background in manufacturing operations, preferably in a regulated setting.
Ability to work effectively in a fast-paced environment while staying focused and on task.
Strong attention to detail in executing procedures and documenting work.
Reliability and punctuality, with consistent presence on scheduled workdays.
Ability to accurately handle labeling and components, including counting and applying FIFO principles.
Capability to follow written SOPs and safety procedures precisely.
Willingness and ability to train others and to learn new equipment and systems.
Additional Skills & Qualifications
Previous experience in a general manufacturing setting is preferred.
Biowork or similar foundational training in biomanufacturing is acceptable.
Comfort working as part of a team-oriented, collaborative production group.
Strong communication skills to support training, documentation, and event response.
Problem-solving mindset to help identify and resolve equipment and quality issues.
Work Environment
This role operates in a regulated, GMP-compliant cleanroom and manufacturing environment that includes filling and packaging areas. The position follows a 2-2-3 shift pattern on a schedule that runs from 6:00 AM to 6:30 PM, supporting round-the-clock production needs. Work involves standing for extended periods, working around production equipment, and wearing appropriate cleanroom and safety attire as required by SOPs. The environment is highly team-oriented, with close collaboration among technicians, and emphasizes safety, quality, and adherence to established procedures.
Job Type & Location
This is a Contract position based out of Clayton, NC.
Pay and Benefits
The pay range for this position is $21.00 - $21.00/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 Clayton, NC.
Application Deadline
This position is anticipated to close on May 7, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACwith four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.
The Manufacturing Technician sets up, operates, monitors, and controls manufacturing equipment, systems, and processes in a regulated, cleanroom environment. This role supports the execution of the production schedule, ensures product quality and compliance with GMP standards, and contributes to a safe, efficient, and highly collaborative manufacturing operation.
Responsibilities
Set up, operate, monitor, and control manufacturing equipment, systems, and processes according to established procedures.
Clean and sanitize manufacturing, filling, and packaging rooms and equipment in accordance with standard operating procedures (SOPs).
Execute the production schedule to meet daily and long-term production goals.
Handle labeling and components accurately, including transferring, counting, applying FIFO (first-in, first-out) practices, and processing returns.
Actively participate in and support event response activities to address production or quality issues.
Review and author SOPs and other controlled documents as required to support continuous improvement and compliance.
Identify, report, and assist in resolving quality issues in a timely and compliant manner.
Execute and assist with equipment maintenance activities, including restoration of lost function, predictive maintenance, and preventative maintenance tasks.
Train fellow employees in areas of personal expertise and proactively learn new systems and equipment beyond current specialization.
Record and review production data in batch production records (BPR) and associated forms with a high degree of accuracy and completeness.
Follow all safety and environmental requirements while performing daily duties.
Perform other related accountabilities and tasks as assigned to support manufacturing operations.
Essential Skills
Previous experience working under GMP (Good Manufacturing Practice) or in a regulated manufacturing environment.
Experience in cleanroom operations and adherence to cleanroom protocols.
Background in manufacturing operations, preferably in a regulated setting.
Ability to work effectively in a fast-paced environment while staying focused and on task.
Strong attention to detail in executing procedures and documenting work.
Reliability and punctuality, with consistent presence on scheduled workdays.
Ability to accurately handle labeling and components, including counting and applying FIFO principles.
Capability to follow written SOPs and safety procedures precisely.
Willingness and ability to train others and to learn new equipment and systems.
Additional Skills & Qualifications
Previous experience in a general manufacturing setting is preferred.
Biowork or similar foundational training in biomanufacturing is acceptable.
Comfort working as part of a team-oriented, collaborative production group.
Strong communication skills to support training, documentation, and event response.
Problem-solving mindset to help identify and resolve equipment and quality issues.
Work Environment
This role operates in a regulated, GMP-compliant cleanroom and manufacturing environment that includes filling and packaging areas. The position follows a 2-2-3 shift pattern on a schedule that runs from 6:00 AM to 6:30 PM, supporting round-the-clock production needs. Work involves standing for extended periods, working around production equipment, and wearing appropriate cleanroom and safety attire as required by SOPs. The environment is highly team-oriented, with close collaboration among technicians, and emphasizes safety, quality, and adherence to established procedures.
Job Type & Location
This is a Contract position based out of Clayton, NC.
Pay and Benefits
The pay range for this position is $21.00 - $21.00/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 Clayton, NC.
Application Deadline
This position is anticipated to close on May 7, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACwith four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.