QA Technician

Actalent; Bedford (OH); On-site; USD 23,000 - 32,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Paid time off

Job summary

Actalent seeks a QA Technician in Bedford, Ohio. This contract role requires performing tests on raw materials, in-process samples, and finished products to ensure quality standards.

You will collect data, maintain records, and collaborate with cross-functional teams to support corrective actions. The role requires lifting up to 50 pounds, standing for extended periods, and strict adherence to cGMP practices.

Qualifications

• Minimum 1 year of work experience in Quality Assurance, Quality Control, or a closely related field.
• Experience in a cGMP environment.
• High school diploma or equivalent.
• Ability to follow established procedures and documentation requirements.
• Strong communication for cross-functional collaboration.
• Ability to collect, interpret, and analyze quality data.
• High ethical standards and commitment to quality compliance.
• Capable of lifting up to 50 pounds unassisted.
• Comfort with standing and moving for extended periods.
• Basic digital literacy to manage documentation and records.

Responsibilities

• Perform tests and inspections on materials and products to verify compliance with quality standards.
• Collect and analyze data from QC activities to identify trends and issues.
• Maintain accurate quality assurance documentation and reports.
• Communicate findings to team members for timely decisions and corrective actions.
• Work with quality engineers, production staff, and supervisors on CAPA actions.
• Support daily production schedules by ensuring timely quality checks.
• Follow procedures to ensure consistency and cGMP compliance.
• Uphold high ethical standards and quality integrity in all tasks.
• Use PPE and follow chemical hygiene guidelines during duties.
• Handle materials safely, including lifting up to 50 pounds and moving as required.

Skills

QA/QC experience

cGMP expertise

Communication

Data analysis

Documentation

Ethics

Lifting 50 lb

Standing/Moving

Digital literacy

Procedures adherence

Education

High School Diploma or Equivalent

Job description

Job Title: QA TechnicianJob Description

Responsibilities

• Perform a range of tests and inspections on raw materials, in-process samples, and finished products to verify compliance with established quality standards.

• Collect and analyze data from quality control activities to identify trends, patterns, and potential quality issues.

• Maintain accurate and up-to-date quality assurance documentation, including test records, inspection reports, and other relevant documents.

• Communicate findings clearly and promptly to relevant team members to support timely decision-making and corrective actions.

• Work closely with quality engineers, production personnel, and supervisors to address quality-related concerns and implement corrective and preventive actions.

• Support the achievement of daily production schedules by ensuring quality checks are completed efficiently and accurately.

• Follow established procedures and documentation practices to ensure consistency and compliance with cGMP requirements.

• Demonstrate high ethical standards by consistently upholding and not compromising quality requirements.

• Use appropriate personal protective equipment and follow chemical hygiene guidelines while performing all duties.

• Handle materials safely, including occasionally lifting and manipulating items up to 50 pounds, and perform tasks that require standing, reaching, bending, stooping, and grasping throughout the shift.

Essential Skills

• Minimum of 1 year of work experience in Quality Assurance, Quality Control, or a closely related field.

• Experience working in a cGMP (current Good Manufacturing Practice) environment.

• High school diploma or equivalent.

• Demonstrated ability to follow established procedures and documentation requirements.

• Strong communication skills to collaborate effectively with cross-functional teams.

• Ability to collect, interpret, and analyze quality control data to identify trends and issues.

• High ethical standards with a strong commitment to maintaining product quality and compliance.

• Capability to occasionally lift up to 50 pounds unassisted.

• Comfort with standing and moving for extended periods, including reaching, bending, stooping, and grasping.

• Basic digital literacy to manage documentation and quality records accurately.

Additional Skills & Qualifications

• Familiarity with quality control and quality assurance principles and practices.

• Experience supporting production environments where adherence to schedules and quality goals is critical.

• Ability to multitask and work effectively in a dynamic, fast-paced team setting.

• Strong attention to detail when performing tests, inspections, and documentation.

• Willingness to consistently use personal protective equipment and follow chemical hygiene practices.

Work Environment

This position is based at a plant facility in Oakwood Village, Ohio, within a Chemical Analysis Division that supports a broad range of industrial and scientific sectors. The work environment is dynamic and fast paced, with a strong emphasis on teamwork, multitasking, and clear communication across quality, production, and supervisory teams. The role involves working in a cGMP-compliant setting where adherence to procedures and documentation standards is essential. The position is categorized as contingent in the United States and may involve scheduling flexibility across Sunday through Saturday. The work requires regular standing and movement, including reaching, bending, stooping, and grasping, as well as occasional lifting and manipulation of materials up to 50 pounds unassisted. Personal Protective Equipment (PPE) is required, and employees must follow chemical hygiene practices to ensure a safe working environment.

Job Type & Location

This is a Contract position based out of Bedford, Ohio.

Pay and Benefits

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

Job Type & Location

This is a Contract position based out of Bedford, Ohio.

Application Deadline

This position is anticipated to close on Nov 18, 2026.

Workplace Type

This is a fully onsite position in Bedford,Ohio.

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.