Validation Specialist

Job Description

Job Description

Job Title: Validation Specialist

Job Description

The Validation Specialist develops, executes, and maintains validation and qualification programs to ensure manufacturing equipment, utilities, processes, and systems meet FDA, cGMP, and internal standards. This role supports sterile injectable manufacturing operations, safeguards product quality, and helps maintain regulatory compliance and inspection readiness in a highly controlled environment.

Responsibilities

• Develop, execute, and maintain validation and qualification programs for manufacturing equipment, utilities, processes, and systems.
• Perform equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for manufacturing systems and production equipment.
• Create, update, and control validation documentation, including Validation Master Plans, User Requirements Specifications, validation protocols, and final summary reports.
• Support the qualification of critical utilities such as HVAC, Water for Injection (WFI), purified water, clean steam, compressed air, and environmental monitoring systems.
• Execute process validations, media fills, cleaning validations, and requalification activities to ensure ongoing compliance and process robustness.
• Conduct risk assessments related to validation activities and document risk-based rationales for validation strategies.
• Investigate validation deviations, identify root causes, and implement corrective and preventive actions.
• Support and evaluate change controls to ensure validated states are maintained when equipment, utilities, or processes change.
• Review validation data for accuracy, completeness, and compliance with applicable regulations and internal procedures.
• Ensure documentation practices align with data integrity principles and meet FDA, cGMP, and company standards.
• Collaborate closely with Engineering, Production, Quality Control, Microbiology, and Quality Assurance teams to plan and execute validation activities.
• Support commissioning activities for new or modified equipment and systems, ensuring smooth transition into validated operation.
• Participate in and support regulatory inspections and internal audits by providing validation documentation and subject matter expertise.
• Contribute to continuous improvement initiatives related to validation, qualification, and overall quality systems.
• Ensure ongoing compliance with FDA regulations, cGMP requirements, data integrity standards, and internal procedures in all validation activities.

Essential Skills

• Bachelor’s degree in Chemistry, Microbiology, Biotechnology, Engineering, Pharmacy, or a related scientific field.
• At least 5 years of validation experience within pharmaceutical manufacturing.
• Hands-on experience supporting sterile injectable manufacturing environments.
• Demonstrated experience with equipment, utility, process, and cleaning validation.
• Strong understanding of FDA cGMP regulations and 21 CFR Parts 210 and 211.
• Working knowledge of Annex 1 sterile manufacturing requirements.
• Experience conducting risk assessments, deviation investigations, and managing change controls.
• Proficiency in developing and executing IQ/OQ/PQ protocols and related validation documentation.
• Knowledge of data integrity principles, including ALCOA+.
• Experience in quality assurance and validation activities within a regulated environment.
• Strong technical writing skills for authoring protocols, reports, and supporting documentation.
• Strong analytical and problem-solving skills with attention to detail.

Additional Skills & Qualifications

• Experience in Chemistry, Microbiology, Biotechnology, or related scientific disciplines.
• Experience working with sterile manufacturing processes and media fills.
• Exposure to Computer System Validation (CSV) in a pharmaceutical or cGMP environment.
• Familiarity with cleaning validation principles and practices.
• Experience collaborating with cross-functional teams including Engineering, Production, Quality Control, Microbiology, and Quality Assurance.
• Ability to interpret and apply regulatory guidance and industry best practices to validation strategies.

Work Environment

The role operates within a cGMP-compliant pharmaceutical manufacturing environment, including clean room areas dedicated to sterile injectable production. Work is performed in highly controlled, regulated spaces where adherence to aseptic techniques, environmental monitoring, and strict documentation practices is essential. The position involves close collaboration with cross-functional teams and regular interaction with production equipment, utilities, and quality systems in a clean room and broader cGMP facility.

This is a Contract to Hire position based out of Boca Raton, FL.

The pay range for this position is $36.06 - $45.67/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)

This is a fully onsite position in Boca Raton,FL.

This position is anticipated to close on Aug 21, 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 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 View email address on ziprecruiter.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.