Patrick Ryan
East Brunswick,New Jersey
Summary
Dynamic chemical manufacturing professional with a proven track record at DuPont, skilled in regulatory compliance and process validation. Expertise in chemical solution preparation and manufacturing oversight, complemented by strong collaboration and problem-solving abilities. Successfully streamlined operations, enhancing efficiency and ensuring adherence to ISO 9001 standards.
Overview
18
18
years of professional experience
Work History
Chemical Manufacturing
DuPont
06.2018 - Current
- Coordinated with regulatory agencies to ensure compliance with all applicable laws and guidelines related to chemical manufacturing processes.
- Ensured regulatory compliance by maintaining up-to-date knowledge on relevant laws, regulations, and guidelines governing chemical manufacturing practices.
- Managed chemical inventory levels, liaising with suppliers to maintain adequate stock for uninterrupted plant operations.
- Streamlined operations through creation of comprehensive process validation protocols and execution of performance qualifications to ensure quality standards.
- Consistently met or exceeded production targets while maintaining strict quality standards, resulting in increased customer satisfaction.
Chenical Operator
Integra Life Sciences
03.2008 - 06.2013
- Managed operation of chemical processing equipment to uphold production quality standards.
- Monitored and adjusted process parameters to maintain compliance with safety standards.
- Conducted routine maintenance on machinery to minimize downtime and enhance efficiency.
- Collaborated with team members to troubleshoot operational issues and implement solutions.
- Recorded and analyzed production data for quality control assessments.
- Trained new operators on standard operating procedures and safety protocols.
- Implemented process improvements that streamlined operations and reduced waste.
- Assisted in the preparation of materials for production runs, ensuring readiness for operations.
- Ensured safe working environment by strictly adhering to safety protocols and guidelines during chemical operations.
- Operated chemical processing equipment successfully while adhering to company standards.
Pharmaceutical Manufacturing Operator
TrisPharma
06.2013 - 2018
- Operated production equipment to ensure efficient pharmaceutical manufacturing processes.
- Monitored quality control measures, maintaining compliance with industry standards.
- Conducted routine maintenance on machinery to prevent operational downtime.
- Collaborated with team members to streamline workflow and improve productivity.
- Assisted in training new operators on safety protocols and equipment handling.
- Documented production data accurately for regulatory compliance and reporting purposes.
- Ensured cleanliness of work area by adhering to proper sanitation protocols both before starting production runs and after their completion.
- Assisted in the successful completion of validation studies for new processes or equipment, ensuring optimal performance and regulatory compliance.
Education
High School Diploma -
Carteret High
Carteret, NJ06.1998
Skills
Chemical manufacturing
Chemical solution preparation
Manufacturing oversight
Manufacturing processes insight
Manufacturing process audits
Toxic industrial chemicals
Chemical neutralization
Chemical storage management
Chemical hazard awareness
Wet chemical processing
Chemical spill response
Manufacturing production scheduling
ISO 9001 manufacturing standards
Manufacturing and production background
Timeline
Chemical Manufacturing
DuPont
06.2018 - Current
Pharmaceutical Manufacturing Operator
TrisPharma
06.2013 - 2018
Chenical Operator
Integra Life Sciences
03.2008 - 06.2013
High School Diploma -
Carteret High