What are the responsibilities and job description for the Aseptic Process Validation Specialist position at Fagron?
Who We Are
Since 1990, we’ve grown into a global leader in personalized medicine. Today, our 5,000 energetic employees are based in 80 locations in Europe, North America, South America, Africa and Asia-Pacific and are working together to support over 200,000 customers worldwide.
From compounding and natural products to software, equipment, and genomics — we deliver smart, ready-to-use solutions that make healthcare better.
We’re passionate, science-driven, and always looking for new ways to improve lives. 🚀
Explore your future at Fagron Career Site.
About The Job
The Aseptic Process Validation Specialist is responsible for planning, executing, and overseeing aseptic process simulations (media fills) to ensure compliance with regulatory requirements and internal quality standards. The role involves coordinating cross-functional teams, documenting processes, analyzing results, and driving continuous improvement initiatives in aseptic operations.
Key Responsibilities
Basic Qualifications
Fagron offers its associates competitive salaries and a wide range of benefits including a 401(k) plan with a company matching contribution; medical, vision and dental; health savings account (HSA); holiday/paid time off.
At Fagron, you’ll find plenty of chances to grow — both personally and professionally. We work in an open, dynamic environment where your ideas and talents can shine.
Ready for the challenge?
We’re proud to be an equal opportunity employer. 🌍 Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.
Fagron US is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.
Since 1990, we’ve grown into a global leader in personalized medicine. Today, our 5,000 energetic employees are based in 80 locations in Europe, North America, South America, Africa and Asia-Pacific and are working together to support over 200,000 customers worldwide.
From compounding and natural products to software, equipment, and genomics — we deliver smart, ready-to-use solutions that make healthcare better.
We’re passionate, science-driven, and always looking for new ways to improve lives. 🚀
Explore your future at Fagron Career Site.
About The Job
The Aseptic Process Validation Specialist is responsible for planning, executing, and overseeing aseptic process simulations (media fills) to ensure compliance with regulatory requirements and internal quality standards. The role involves coordinating cross-functional teams, documenting processes, analyzing results, and driving continuous improvement initiatives in aseptic operations.
Key Responsibilities
- Process Simulation Execution:
- Plan, schedule, and execute aseptic process simulations (media fills) in accordance with regulatory guidelines (e.g., FDA, Boards of Pharmacy).
- Ensure the sterile environment and practices adhere to validated aseptic techniques.
- Documentation and Reporting:
- Prepare and maintain comprehensive records of media fill protocols, results, and deviations.
- Generate and present reports summarizing APS findings, trends, and corrective actions to management.
- Compliance and Quality Assurance:
- Ensure APS activities comply with cGMP, regulatory, and company standards.
- Act as a liaison during internal and external audits related to aseptic processing.
- Team Coordination:
- Collaborate with production, quality, and validation teams to ensure readiness for APS activities.
- Train personnel on aseptic techniques and media fill protocols.
- Continuous Improvement:
- Analyze APS outcomes to identify process gaps or improvement opportunities.
- Propose and implement corrective and preventive actions (CAPA) to enhance aseptic processes.
- Risk Assessment and Troubleshooting:
- Perform risk assessments related to APS execution and aseptic processing.
- Troubleshoot issues encountered during simulations and ensure timely resolution.
- Key Performance Indicators (KPIs)
- Timeliness and compliance of APS execution.
- Accuracy and completeness of APS documentation.
- Reduction in APS-related deviations and implementation of CAPA.
- Continuous improvement in aseptic process efficiency.
Basic Qualifications
- Strong knowledge of cGMP, FDA, and other relevant regulatory requirements.
- Excellent organizational and project management skills.
- Proficiency in data analysis and technical writing.
- Effective communication and interpersonal skills for cross-functional collaboration.
- Work in cleanroom environments requiring adherence to strict gowning procedures.
- Ability to work flexible hours to accommodate media fill schedules.
Fagron offers its associates competitive salaries and a wide range of benefits including a 401(k) plan with a company matching contribution; medical, vision and dental; health savings account (HSA); holiday/paid time off.
At Fagron, you’ll find plenty of chances to grow — both personally and professionally. We work in an open, dynamic environment where your ideas and talents can shine.
Ready for the challenge?
We’re proud to be an equal opportunity employer. 🌍 Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.
Fagron US is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.