Jr Validation Engineer

Actalent; Westerville (OH); On-site; USD 40,000 - 56,000; Full time

Benefits offered by this job

Onsite role

Contract-to-hire

Job summary

Actalent is seeking an Equipment Validation Engineer to support validation activities, author documentation, and assist with change control within a GMP-regulated manufacturing environment. The role blends office-based documentation with hands-on exposure to manufacturing operations, based in Columbus, OH.

Responsibilities include validating equipment, maintaining protocols, and collaborating with engineering and manufacturing teams to ensure adherence to GMP standards.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related technical field OR equivalent pharmaceutical manufacturing experience.
• 0-2 years of professional experience.
• Strong written and verbal communication skills.

Responsibilities

• Support equipment validation activities for manufacturing equipment and systems.
• Author, revise, and maintain validation protocols and documentation.
• Execute validation activities and ensure compliance with established procedures.
• Support change control processes related to equipment modifications and maintenance.
• Update and maintain SOPs, work instructions, and operational procedures.
• Partner with engineering and manufacturing teams during equipment installations and modifications.
• Provide validation support for equipment changes and system improvements.
• Assist with continuous improvement initiatives within manufacturing operations.
• Ensure compliance with GMP regulations and validation standards.
• Participate in investigations, risk assessments, and documentation reviews as required.
• Monitor CPPs and CQAs related to validated processes.

Skills

Validation

Protocols

CPP

CQA

SOP

Education

Bachelor's degree in Engineering or Life Sciences

Job description

Job Description The Equipment Validation Engineer will support equipment validation activities, author and execute validation documentation, assist with change control processes, and collaborate with manufacturing and engineering teams to ensure compliance with GMP requirements. This position offers a blend of office-based technical documentation work and hands-on exposure to manufacturing operations.

Validation Engineer Job Description The Equipment Validation Engineer will support equipment validation activities, author and execute validation documentation, assist with change control processes, and collaborate with manufacturing and engineering teams to ensure compliance with GMP requirements. This position offers a blend of office-based technical documentation work and hands-on exposure to manufacturing operations.

Responsibilities

• Support equipment validation activities for manufacturing equipment and systems.
• Author, revise, and maintain validation protocols and documentation.
• Execute validation activities and ensure compliance with established procedures.
• Support change control processes related to equipment modifications and maintenance.
• Update and maintain SOPs, work instructions, and operational procedures.
• Partner with engineering and manufacturing teams during equipment installations and modifications.
• Provide validation support for equipment changes and system improvements.
• Assist with continuous improvement initiatives within manufacturing operations.
• Ensure compliance with GMP regulations and validation standards.
• Participate in investigations, risk assessments, and documentation reviews as required.
• Monitor critical process parameters (CPPs) and critical quality attributes (CQAs) related to validated processes.

Essential Skills

• Knowledge in validation, validation protocols, process validation, and validation testing.
• Experience with equipment validation, CPP, CQA, risk assessment, SOP, and work instruction.
• Bachelor's degree in Engineering, Life Sciences, or a related technical field OR equivalent pharmaceutical manufacturing experience.
• 0-2 years of professional experience.
• Strong written and verbal communication skills.
• Ability to work independently and take ownership of assigned responsibilities.
• Strong organizational and problem-solving abilities.
• Demonstrated initiative and willingness to learn in a regulated environment.
• Familiarity with GMP, pharmaceutical, and engineering technical documentation.

Additional Skills & Qualifications

• Internship, co-op, or academic project experience in manufacturing or engineering environments.
• Experience working in a pharmaceutical, biotechnology, medical device, or regulated manufacturing environment.
• Familiarity with GMP regulations, validation, or quality systems.
• Experience authoring technical documentation or procedures.
• Exposure to process improvement initiatives.

Job Type & Location

This is a Contract to Hire position based out of Columbus, OH.

Pay And Benefits

The pay range for this position is $28.85 - $40.87/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)
• Workplace Type This is a fully onsite position in Columbus,OH.
• Application Deadline This position is anticipated to close on Oct 7, 2026.

About Actalent

Actalent is a global leader in engineering & 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.