Actalent
Job Title: Validation Engineer II
Job Description
We are seeking a highly detail-oriented Validation Engineer II to support the qualification and validation of laboratory equipment, with a strong emphasis on sanitization processes. This role is critical to ensuring compliance with regulatory standards and internal quality systems in a GMP-regulated environment.
Responsibilities
Carry out hands-on testing and qualification of equipment used in manufacturing and cleanroom environments.
Run and document validation protocols (IQ/OQ/PQ) for sterilization systems and related machinery.
Work directly with systems like autoclaves, SIP (Steam-in-Place), CIP (Clean-in-Place), and dry heat sterilizers to ensure proper function and compliance.
Perform temperature mapping and other studies to verify equipment performance.
Partner with teams across engineering, manufacturing, and quality to keep projects on track and compliant.
Help prepare for inspections by organizing validation records and offering technical insights.
Essential Skills
Experience in sanitization, validation, GMP, and sterilization.
Strong ability to organize and document.
Detail-oriented approach to tasks.
Additional Skills & Qualifications
Bachelor’s degree in engineering, life sciences, or a related discipline.
3–7+ years of experience in validation within the pharmaceutical or biotech industry.
Strong hands-on experience with sterilization systems including SIP, CIP, autoclaves, and dry heat.
Solid grasp of IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) processes.
Ability to work independently and take initiative with minimal guidance.
Comfortable working in a fast-paced environment and responding quickly to project needs.
Work Environment
This position operates within a laboratory environment, where you will engage with advanced sterilization systems and processes. The role requires adaptability and the ability to respond swiftly to project demands.
Job Type & Location
This is a Contract position based out of Silver Spring, Maryland.
Pay and Benefits
The pay range for this position is $52.88 - $57.69/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 Silver Spring,MD.
Application Deadline
This position is anticipated to close on Oct 8, 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.
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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
We are seeking a highly detail-oriented Validation Engineer II to support the qualification and validation of laboratory equipment, with a strong emphasis on sanitization processes. This role is critical to ensuring compliance with regulatory standards and internal quality systems in a GMP-regulated environment.
Responsibilities
Carry out hands-on testing and qualification of equipment used in manufacturing and cleanroom environments.
Run and document validation protocols (IQ/OQ/PQ) for sterilization systems and related machinery.
Work directly with systems like autoclaves, SIP (Steam-in-Place), CIP (Clean-in-Place), and dry heat sterilizers to ensure proper function and compliance.
Perform temperature mapping and other studies to verify equipment performance.
Partner with teams across engineering, manufacturing, and quality to keep projects on track and compliant.
Help prepare for inspections by organizing validation records and offering technical insights.
Essential Skills
Experience in sanitization, validation, GMP, and sterilization.
Strong ability to organize and document.
Detail-oriented approach to tasks.
Additional Skills & Qualifications
Bachelor’s degree in engineering, life sciences, or a related discipline.
3–7+ years of experience in validation within the pharmaceutical or biotech industry.
Strong hands-on experience with sterilization systems including SIP, CIP, autoclaves, and dry heat.
Solid grasp of IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) processes.
Ability to work independently and take initiative with minimal guidance.
Comfortable working in a fast-paced environment and responding quickly to project needs.
Work Environment
This position operates within a laboratory environment, where you will engage with advanced sterilization systems and processes. The role requires adaptability and the ability to respond swiftly to project demands.
Job Type & Location
This is a Contract position based out of Silver Spring, Maryland.
Pay and Benefits
The pay range for this position is $52.88 - $57.69/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 Silver Spring,MD.
Application Deadline
This position is anticipated to close on Oct 8, 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.
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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.