Visual Inspection Operator

Actively Interviewing for Visual Inspection Operator to join CDMO in Birmingham, AL!

Job Description

The Visual Inspection Operator plays a critical role in ensuring that finished products meet rigorous quality and safety standards before they reach customers. This position suits someone who is highly detail-oriented, dependable, and comfortable performing repetitive tasks while following precise procedures in a fast-paced pharmaceutical manufacturing environment. The role offers opportunities for cross-training and internal advancement within a supportive, growth-focused culture.

Responsibilities

• Conduct manual visual inspections of finished products to identify defects, flaws, or nonconformities as defined by established procedures and criteria.
• Individually manipulate and examine each unit to verify that it meets all quality and regulatory standards.
• Carry out operational tasks by following established processes and working within defined settings or parameters.
• Perform routine activities such as finished product sampling, labeling, and final packaging.
• Operate basic machinery, tools, and equipment according to documented protocols and work instructions.
• Assist in equipment installation and maintenance by preparing materials and following detailed instructions.
• Support the quality function by working within strict Good Manufacturing Practice (GMP) and quality control standards.
• Follow mandatory work instructions, including the correct use of personal protective equipment (PPE), to safeguard the environment and the wellbeing of oneself and others.
• Record numerical data accurately and complete required documentation in a timely and precise manner.
• Perform basic math calculations as needed to support inspection and production activities.
• Handle chemicals safely and follow procedures related to chemical handling, wet chemistry, and testing where applicable.
• Support laboratory and cleanroom practices by maintaining cleanliness, order, and compliance with regulatory expectations.
• Communicate effectively with team members and supervisors to coordinate workflow and ensure smooth operations.
• Participate in cross-training opportunities to expand skills across laboratory, manufacturing, and quality-related tasks.

Essential Skills

• Strong attention to detail and the ability to identify defects or nonconformities during manual visual inspection.
• Ability to follow detailed written procedures, work instructions, and established processes consistently.
• Comfort with repetitive tasks while maintaining focus, accuracy, and quality.
• Basic math skills and the ability to record numerical data accurately.
• Familiarity with Good Manufacturing Practices (GMP) and quality control principles, or the ability to learn them quickly.
• Ability to operate basic machinery, tools, and equipment in a manufacturing or laboratory environment.
• Willingness and ability to follow safety procedures, including proper use of personal protective equipment (PPE).
• Effective communication skills to work collaboratively with team members and supervisors.
• Dependability, punctuality, and a strong sense of responsibility for product quality and safety.

Additional Skills & Qualifications

• Experience in a laboratory setting is a plus.
• Bachelor's degree preferred, particularly in chemistry or a related scientific discipline.
• Exposure to cleanroom environments and laboratory operations is beneficial.
• Experience with chemical handling, wet chemistry, or chemical testing is advantageous.
• Understanding of pharmaceutical manufacturing processes and regulatory expectations is a strong asset.
• Ability to support quality assurance and quality control activities within strict standards.
• Interest in cross-training and developing skills across multiple functions, including manufacturing, laboratory, and quality.
• Motivation to grow within a company that promotes from within and supports career development.

Work Environment

This position is based 100% on site in a pharmaceutical laboratory and cleanroom environment. You will work around manufacturing processes, laboratory equipment, and chemicals, following strict GMP, quality, and safety standards. The standard schedule is Monday through Friday, 7:00 a.m. to 4:00 p.m., with the potential for overtime and holiday work as business needs arise. Shift changes are expected in the future, so some flexibility with working hours is important. The role requires adherence to cleanroom protocols and the use of appropriate personal protective equipment (PPE) in designated areas. The work setting is structured, process-driven, and highly regulated, with a culture that emphasizes quality, safety, collaboration, and opportunities for cross-training and internal promotion.

Job Type & Location

This is a Contract position based out of Birmingham, AL.

Pay and Benefits

The pay range for this position is $25.00 - $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 Birmingham,AL.

Application Deadline

This position is anticipated to close on May 29, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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.