Job Title: Lead Manufacturing Technician
Job Description
The Lead Manufacturing Technician operates advanced automated equipment to support the formulation, preparation, and dispensing of pharmaceutical products in accordance with cGMP guidelines. This role serves as a lead technician on the production floor, coordinating work activities, reviewing documentation, and ensuring that all processes comply with standard operating procedures (SOPs). The technician contributes directly to the production of life-saving diagnostic drug products and plays a key role in maintaining high-quality, compliant manufacturing operations.
Responsibilities
Operate advanced automated equipment to perform formulation, preparation, and dispensing of pharmaceutical products in compliance with cGMP guidelines.
Execute all manufacturing tasks in accordance with standard operating procedures (SOPs) and established production processes.
Perform accurate and timely documentation of all manufacturing activities in line with cGMP requirements.
Properly review batch records to ensure completeness, accuracy, and compliance with regulatory and internal quality standards.
Provide leadership on the production floor by coordinating work among technicians and supporting daily production priorities.
Assist in the creation and manufacture of new products by following defined processes and operating specialized equipment.
Provide front-line troubleshooting of manufacturing equipment and process issues, and escalate concerns to appropriate personnel when necessary.
Follow cleanroom procedures and aseptic techniques to maintain a sterile production environment.
Support packaging and production operations as needed to meet production demands and schedules.
Adhere to all safety procedures, including those related to working with radioactive materials and advanced equipment.
Participate actively in safety programs designed to minimize potential and actual exposure levels.
Maintain close attention to detail to ensure product quality, accurate documentation, and compliance with regulatory requirements.
Collaborate with team members in a team-based environment to achieve production goals and continuous improvement objectives.
Perform physical tasks such as lifting, walking, bending, stooping, pushing, pulling, reaching, and climbing stairs as required to complete production activities.
Handle radioactive cyclotron components frequently and use personal protective equipment as required by procedures.
Work rotating schedules and outside regular work hours as needed to support continuous production operations.
Essential Skills
Three to five years of relevant work experience, preferably in a pharmaceutical or manufacturing industry.
Experience working in an FDA-regulated cGMP environment is preferred.
Strong mechanical aptitude with the ability to understand and operate advanced automated manufacturing equipment.
Demonstrated ability to perform documentation in accordance with cGMP guidelines.
Experience reviewing batch records for completeness, accuracy, and compliance.
Capability to provide front-line troubleshooting of manufacturing equipment and process issues.
Ability to properly elevate equipment and process concerns to appropriate personnel.
Familiarity with cleanroom operations and sterile production environments.
Strong attention to detail and commitment to quality and compliance.
Good hand-eye coordination to safely and accurately operate equipment and handle components.
Willingness and ability to work rotating schedules and outside regular work hours.
Ability to perform physical activities such as lifting up to 70 lbs, walking, bending, stooping, pushing, pulling, reaching, and climbing stairs, with or without accommodation.
Comfort working in a plant producing radioactive materials and adhering to strict safety procedures.
Additional Skills & Qualifications
Associate Degree or completion of an equivalent certification program from a technical or vocational school, or equivalent relevant years of experience in a related field.
Scientific background is preferred and beneficial for understanding pharmaceutical processes.
Experience in pharmaceutical production, packaging, or other cGMP processing environments.
background in manufacturing or processing in a regulated environment.
Ability to work effectively in a team-based environment and provide leadership on the production floor.
Interest in career growth within an advanced developmental path where many supervisors have progressed from technician roles.
Work Environment
This role operates within a sterile, cleanroom production environment with defined gowning requirements. The position follows a rotating 10-hour schedule, including: Week 1 (Sunday-Wednesday, 5:00 p.m. - 3:30 a.m.), Week 2 (Monday-Wednesday, 5:00 p.m. - 3:30 a.m.), and Week 3 (Saturday-Tuesday, 5:00 p.m. - 3:30 a.m.). The facility produces radioactive materials, and all employees participate in comprehensive safety programs designed to minimize potential and actual exposure levels. Team members frequently handle radioactive cyclotron components and must be willing to wear a variety of personal protective equipment as required. The work environment emphasizes close attention to detail, adherence to cGMP and FDA regulations, and collaboration in a team-based setting. The role may require sitting or standing for long periods and occasional lifting of up to 70 lbs, along with physical activities such as walking, bending, stooping, pushing, pulling, reaching, and climbing stairs, with or without accommodation. The position offers the opportunity to work with advanced equipment, contribute to life-saving diagnostic drug products, and grow within a structured, career-development-focused environment.
Job Type & Location
This is a Contract to Hire position based out of Maryland Heights, MO.
Pay and Benefits
The pay range for this position is $29.04 - $30.00/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 Maryland Heights,MO.
Application Deadline
This position is anticipated to close on Jun 25, 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 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.
