Quality Control Technician

Actalent; Dayton (OH); Presencial; USD 28.000 - 40.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

HSA

Transportation benefits

PTO / Vacation / Sick Leave

Descripción de la vacante

Actalent is hiring multiple Quality Technician roles in the Dayton, OH area for positions in a highly regulated medical manufacturing environment. Candidates with a high school diploma and quality experience in FDA/GMP/GDP settings are preferred.

Roles span 1st, 2nd, and 3rd shifts and involve working onsite in Dayton, OH. The Quality Technician supports quality assurance activities, ensures non-conforming materials are identified and documented, and maintains compliance with FDA, ISO, and

Formación

• High school diploma or equivalent.
• Prior experience working in a quality role in a highly regulated environment (e.g. FDA, GMP, GDP, etc.).

Responsabilidades

• Perform issuance of controlled documentation in accordance with established procedures.
• Review batch records and manufacturing records to ensure they are organized, quickly retrievable, accurate, complete, and free of errors, following GDP.
• Support chain of custody activities for bulk and labeled drug products, ensuring traceability and compliance.
• Assist cross-functional teams in problem solving and root cause analysis for quality events.
• Work within the Quality Management System (QMS) to support to all cGMP departments.
• Perform material inspection activities to support processing and distribution sites, including incoming material inspections, in-process inspections, and finished product inspections.
• Maintain accurate, complete, and compliant records of all activities, following Good Documentation Practices.
• Work with peers and management to ensure compliance with all Quality Management System requirements and applicable regulations.
• Support internal and external audits as assigned, providing documentation, explanations, and follow-up actions as needed.

Educación

High school diploma or equivalent

Descripción del empleo

Quality Technician

We are hiring for multiple Quality Technician roles in the Dayton, Ohio area! These roles will be working within a highly regulated medical manufacturing environment. Ideal candidates will have at least a High School Diploma or GED and quality experience in a highly regulated environment (FDA, GMP, GDP, etc.). These positions range across 1st, 2nd and 3rd shifts.

Quality Technician The Quality Technician supports quality assurance activities for manufacturing and distribution processes, ensuring that non-conforming materials and products are identified, controlled, and managed in accordance with the Quality System. This role follows all policies and procedures to maintain compliance with FDA, AATB, OSHA, ISO, and related regulatory standards. The Quality Technician works under limited supervision, handling a range of products including medical devices, sterile processed human tissue-based products, biologics, unprocessed human tissue, component supplies, and labeling materials.

Responsibilities

• Perform issuance of controlled documentation in accordance with established procedures.
• Review batch records and manufacturing records to ensure they are organized, quickly retrievable, accurate, complete, and free of errors, following Good Documentation Practices (GDP).
• Support chain of custody activities for bulk and labeled drug products, ensuring traceability and compliance.
• Assist cross-functional teams in problem solving and root cause analysis for quality events.
• Work within the Quality Management System (QMS) to support to all cGMP departments.
• Perform material inspection activities to support processing and distribution sites, including incoming material inspections, in-process inspections, and finished product inspections.
• Maintain accurate, complete, and compliant records of all activities, following Good Documentation Practices.
• Work with peers and management to ensure compliance with all Quality Management System requirements and applicable regulations.
• Support internal and external audits as assigned, providing documentation, explanations, and follow-up actions as needed.

Qualifications

• High school diploma or equivalent.
• Prior experience working in a quality role in a highly regulated environment (e.g. FDA, GMP, GDP, etc.).

Job Type & Location
This is a Contract position based out of Dayton, OH.

Pay and Benefits

The pay range for this position is $24.50 - $24.50/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)

Job Type & Location
This is a Contract position based out of Dayton, OH.

Application Deadline
This position is anticipated to close on Oct 26, 2026.

Workplace Type
This is a fully onsite position in Dayton,OH.

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 [e-mail] 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.