Job Title: Quality Inspector
Job Description

The Quality Inspector will work under the direction of the Quality Inspector Supervisor in a c-GMP regulated manufacturing environment operating under Q7A standards. This is a contract position that may become permanent and is intended to cover for employees on leave. The role involves minimal paperwork but requires basic computer skills, such as sending coherent emails with daily findings. Good communication skills are essential as the inspector will interact with operators to address and communicate issues found during inspections.

ResponsibilitiesUphold all standards of quality assurance compliance.Ensure GMP checklist and all other procedures are actively followed.Support good manufacturing practices and good documentation practices in the plant.Educate employees and document instances based on GMP observations.Be the point-of-contact for GMP questions and improvements from employees.Maintain a thorough audit log of GMP improvement opportunities.Follow through with corrective and preventative actions (CAPA) on GMP program compliance.Act as a liaison and educator for quality compliance and continuous improvement.Perform all requested quality tests for equipment and room approval.Work in extreme cold and hot environments (up to 120 F).Comprehend oral and written English instructions.Lift up to 55 pounds and drive a forklift safely and efficiently.Follow established policies and procedures.Operate and maintain chemical processing equipment.Exhibit manual dexterity, perceptual speed, and flexibility.Adapt to rapidly changing priorities based on business needs.Pass a pre-employment physical with drug screen and physical capabilities test.Squat to touch the floor 10 times without assistance.Lift a graduated weight up to 55 pounds from 4” to 57”.Stack 40, 55 lbs. bags within 10 minutes.Push at least 102 lbs. from any height.Pull an average of 100 lbs. at 36”.Ascend/descend a vertical ladder for 15 rungs (8 rungs 2 times).Lift 30 lbs. to workers' overhead extension for one repetition.Simulate scraping movement: 20 lbs. CW/CCW for 2 minutes at 18 inches height.Simulate opening/closing a valve with a crossbar at 60 inches height.Maneuver 185 lbs. from the floor to 4 inches one time.Essential SkillsKnowledge of theories, principles, and methods of quality assurance programs.Understanding of GMP from a pharmaceutical and/or food safety perspective.Good Documentation Practices.Good Manufacturing Practices.Understanding of scientific methods and technical/mechanical processes.Experience in an FDA ICH-Q7 and 21 CFR 117 environment.Strong communication and collaborative skills.Ability to work effectively and efficiently on multiple projects at once.Ability to work effectively in a team environment.Ability to respond to rapidly changing demands.Additional Skills & QualificationsHigh School Diploma or GED.Work Environment

The Quality Inspector will work as part of a very collaborative team environment. 75% of the time will be spent on the production floor, which includes moving between buildings and navigating stairs (one line is three stories tall). The role requires working in extreme temperature conditions.

Pay and Benefits

The pay range for this position is $23.00 - $25.00/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 Saint Louis,MO.

Application Deadline

This position is anticipated to close on Feb 4, 2025.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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

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.