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Actalent
Validation Support Specialist
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What they do
A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.
$92,582 / year median in the U.S.
+6% projected growth
Job Description
Job Title:
Validation Support Specialist Job Description The Validation Support Specialist executes qualification and validation activities for autoclaves and washers used in manufacturing operations. This role follows pre-approvedIQ/OQ/PQ
protocols, accurately records data and documents results in accordance with Good Documentation Practices, and supports equipment qualification and validation efforts in a regulated manufacturing environment. The position offers an opportunity to gain experience and establish a career within a large pharmaceutical manufacturing setting. Responsibilities Execute autoclave qualification and validation activities in alignment with approved protocols and established procedures. Perform washer qualification and validation cycles to ensure equipment operates reliably and meets defined specifications. Follow and execute pre-approvedIQ/OQ/PQ
protocols with a high level of accuracy and compliance. Accurately record data and document results in accordance with Good Documentation Practices (GDP) and internal documentation standards. Support equipment qualification and validation efforts for manufacturing operations by assisting with test execution and data collection. Verify that validation activities are completed according to established procedures, protocols, and regulatory expectations. Maintain accurate, organized, and up-to-date validation documentation for audits, reviews, and ongoing operations. Collaborate with validation and manufacturing teams to support project timelines and ensure validation tasks are completed on schedule. Identify and communicate documentation discrepancies or protocol deviations promptly to the appropriate stakeholders. Assist with data entry and documentation updates related to validation and qualification activities. Demonstrate willingness to learn new processes and tools to support evolving validation and manufacturing needs. Essential Skills Minimum of 1 year of experience in pharmaceutical, biotechnology, or other regulated manufacturing environments. Experience operating autoclaves and/or washers in a manufacturing setting. Ability to follow detailed written procedures and protocols accurately and consistently. Understanding of Good Documentation Practices (GDP) and their application to validation activities. Strong attention to detail and organizational skills when handling validation data and documentation. Self-motivated mindset with a strong work ethic and commitment to completing tasks thoroughly. Ability to learn new processes quickly and apply training to day-to-day validation work. Capability to work independently when needed while still collaborating effectively with cross-functional teams. Previous experience in validation, commissioning, qualification, or quality support activities. Exposure toIQ/OQ/PQ
activities in a GMP-regulated environment. Experience working in GMP-regulated environments and understanding of basic GMP principles. Proficiency in data entry with a focus on accuracy and completeness. Additional Skills & Qualifications Demonstrated willingness to learn and adapt to new validation tools, systems, and procedures. Ability to communicate clearly and professionally with validation and manufacturing team members. Comfort working with technical documentation and validation protocols. Strong sense of ownership and accountability for assigned validation tasks and documentation. Interest in building a long-term career in validation, quality, or manufacturing support within the life sciences industry. Previous involvement in equipment qualification projects or quality support initiatives is beneficial. Work Environment This role is fully onsite Monday through Friday in a GMP-regulated pharmaceutical manufacturing environment. Standard daytime hours are expected, with no routine overtime anticipated. The position involves working around manufacturing equipment such as autoclaves and washers and handling technical documentation and data entry tasks. You will collaborate closely with validation and manufacturing teams in a structured, process-driven setting that emphasizes compliance, accuracy, and safety. The environment offers an opportunity to gain valuable hands-on experience and establish a foothold in large-scale pharmaceutical manufacturing. Job Type & Location This is a Contract position based out of Sanford, NC. Pay and Benefits The pay range for this position is $25.00 - $27.00/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 Sanford,NC.