Job Information
Actalent Process Control Technologist in Syracuse, New York
Job Title: Process Control Technologist III / Validation SpecialistJob Description
We are seeking an experienced Validation Specialist for the position of Process Control Technologist III. The ideal candidate will have extensive experience in equipment, process, and computer/control system validation within a pharmaceutical manufacturing environment.
Responsibilities
Design, conduct, and report validation studies for equipment and processes, including FAT, SAT, IQ, OQ, PQ, and PPQ.
Complete all aspects of the validation process, including design/development, writing validation protocols, executing validation studies, and writing final reports.
Coordinate and execute validation studies with production, QA, QC, materials management, and other internal departments.
Perform test runs in compliance with protocols and SOPs, completing proper documentation.
Compile and analyze data collected during test runs, including creating graphs, charts, or tables as needed.
Participate in project teams for new equipment and processes, providing input on validation requirements, resources, and timing.
Develop new product and facility validation strategies.
Complete validation maintenance, including confirmations, continued process verifications, and periodic revalidation studies.
Provide training and guidance to less experienced staff and review their work.
Support change control administration, evaluating changes for impact on validations and calibrations.
Work with customers, vendors, and external service providers to complete validations.
Represent the department at audits and assist in CAPA development and implementation.
Essential Skills
Bachelor’s degree in sciences or equivalent; master’s degree is a plus.
5+ years in the pharmaceutical validation field; experience with sterile product/process validation is a plus.
Experience administering a change control program in a regulated industry.
Exceptional technical writing skills.
Knowledge of contemporary validation practices and procedures in a pharmaceutical manufacturing environment.
Proficiency in using computer software, including databases, spreadsheets, and word processing.
Ability to operate specialized equipment, such as temperature datalogging systems.
Understanding of cGMPs, industry standards, and validation guidelines.
Attention to detail and ability to manage multiple projects, priorities, and deadlines.
Strong communication skills with coworkers and management.
Additional Skills & Qualifications
Membership in specialized groups and committees, as assigned.
Ability to review, edit, and approve SOP revisions ensuring compliance with validations.
Work Environment
The work schedule is Monday to Friday, from 7:30 AM to 4 PM. Working days and hours may vary based on the production schedule.
Job Type & Location
This is a Permanent position based out of Syracuse, NY.
Pay and Benefits
The pay range for this position is $90000.00 - $90000.00/yr.
Company Benefits Company Benefits Company Benefits • 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 Syracuse,NY.
Application Deadline
This position is anticipated to close on Mar 31, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.