Manufacturing Technician Filling 1st Shift

About the role

The Manufacturing Technician – Filling supports all aspects of production and quality control testing of raw and in-process materials for transplant diagnostics products. This role focuses on the accurate dispensing and packaging of biological reagents, preparation of reagents and buffer solutions, operation of production equipment in a laboratory/cleanroom environment, while adhering to Good Manufacturing Practices (GMP) and established laboratory procedures.

Responsibilities

• Follow standard operating procedures to ensure high-quality assay manufacturing.
• Dispense biological reagents accurately and consistently according to production requirements.
• Prepare reagents and buffer solutions following written laboratory procedures.
• Print labels and label bottles, vials, and boxes accurately for traceability and compliance.
• Package, seal, and scan assays to prepare finished products for distribution.
• Perform production tasks across different product lines as needed to support manufacturing demands.
• Set up and operate equipment of moderate complexity in accordance with safety and quality standards.
• Maintain a clean, safe, and organized work environment in laboratory and production areas.
• Protect the confidentiality of laboratory data, processes, and proprietary information.
• Efficiently handle multiple tasks and projects simultaneously while meeting deadlines.
• Organize work and maintain assigned work schedules, including consistent 1st shift attendance.
• Maintain a clean, safe, and organized work environment in laboratory and production areas.
• Protect the confidentiality of laboratory data, processes, and proprietary information.
• Follow GMP and laboratory best practices to ensure compliance with regulatory and quality standards.

Requirements

• Bachelor’s degree in Biological Sciences, Chemistry, or a related field from an accredited institution.
• Two (2) years of laboratory experience.
• Knowledge of standard laboratory procedures and practices.
• Ability to read, understand, and implement written laboratory procedures and protocols.
• Ability to handle and work safely with biological and chemical reagents.
• Basic proficiency with Microsoft Word and Excel.
• Ability to organize work effectively and maintain assigned work schedules.
• Ability to set up and operate laboratory and production equipment of moderate complexity.
• Capability to work in a laboratory/cleanroom environment and follow GMP principles.
• Experience in manufacturing, production, or GMP-regulated environments.
• Experience or exposure to large-scale manufacturing or kit production.
• Experience with inventory control, staging, and production support activities.
• Strong attention to detail and commitment to quality in a regulated setting.
• Ability to manage multiple tasks and projects simultaneously in a fast-paced environment.
• Strong problem-solving skills and willingness to assist in process improvement and protocol development.
• Interest in building a career in science, manufacturing, or transplant diagnostics.
• Willingness to learn new techniques and processes with on-the-job training.

Qualifications

• Experience in manufacturing, production, or GMP-regulated environments.
• Experience or exposure to large-scale manufacturing or kit production.
• Experience with inventory control, staging, and production support activities.
• Strong attention to detail and commitment to quality in a regulated setting.
• Ability to manage multiple tasks and projects simultaneously in a fast-paced environment.
• Strong problem-solving skills and willingness to assist in process improvement and protocol development.
• Interest in building a career in science, manufacturing, or transplant diagnostics.
• Willingness to learn new techniques and processes with on-the-job training.

Skills

• Biological Sciences, Chemistry, or related field education.
• Laboratory experience.
• Standard laboratory procedures and practices knowledge.
• Microsoft Word and Excel proficiency.
• Inventory control, staging, and production support activities experience.
• Problem-solving skills.
• Process improvement and protocol development interest.
• New technique and process learning ability.

Benefits

• Medical, dental & vision coverage.
• Critical Illness, Accident, and Hospital coverage.
• 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 coverage.
• Health Spending Account (HSA).
• Transportation benefits.
• Employee Assistance Program.
• Time Off/Leave (PTO, Vacation or Sick Leave).

Pay and Benefits

The pay range for this position is $20.00 - $20.00/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:

Work Environment

This role operates in a laboratory and cleanroom production environment on a 1st shift schedule, typically from 6:00 a.m. to 2:30 p.m. Work frequently takes place at laboratory workstations, low-temperature freezers, and computer workstations, with regular use of laboratory and production equipment of moderate complexity. The position involves handling biological and chemical reagents and requires adherence to GMP standards, laboratory safety procedures, and cleanroom practices. The role may require lifting objects, including laboratory instrumentation, up to 35 pounds. The environment supports professional growth in kit production, large-scale manufacturing, and regulated laboratory operations, offering opportunities to gain and expand GMP experience within a structured and collaborative setting.

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.