Monte Adams
Raleigh,US
Summary
I am a highly motivated and established leader with over 16 years of manufacturing experience. Skilled processes improvement specialist with a vast knowledge of cGMP and clean room manufacturing within Grades A, B, C and D. Expert at creating and implementing streamline training programs to provide guidance and mentoring of employees, all while maximizing productivity goals and safety throughout.
Overview
16
16
years of professional experience
Work History
ASEPTIC TECHNICIAN II
Pfizer
03.2020 - 07.2025
- Trained in clean room technique, design/processes and gowning of ISO 5/EU Grade A/B areas.
- Provided consistent application of both technical and regulatory knowledge to drive production within the manufacturing suite to meet customer and business goals.
- Acted as the manufacturing point person on the floor for manufacturing processes and called upon to make real-time decisions on a wide range of production issues.
- Ensured that when quality-related issues arise, the issues are quickly elevated with proper documentation of the events and if needed, any corrective or preventative actions, which resulted in a team effort with multiple functional departments.
- Worked with corporate Aseptic compliance to identify process improvements for filling equipment set up and interventions.
- Monitored and adjusted production equipment to ensure quality of the product and increase productivity.
- Enhanced product quality by conducting thorough formulation testing and analysis.
Formulation Technician
Pfizer
08.2015 - 03.2020
- Streamlined manufacturing processes for increased efficiency by optimizing formulations.
- Developed new formulations with improved performance, resulting in satisfied customers and increased sales.
- Collaborated with cross-functional teams to ensure successful product launches and meet project deadlines.
FILLING TECHNICIAN AND FORMULATION
Hospira, a Pfizer Company
03.2009 - 08.2015
- In charge of setting up, repairing, cleaning and oversight of the production lines in a Terminally Sterilized ISO Grade 8D/7C controlled area, ensuring that all production goals were achieved while using and implementing plant and corporate SOP's.
- Troubleshot and repaired solution equipment such as pumps, conveyors and filling needles while using manuals, SOP's and specifications required by 21 Code of Federal Regulations (CFR) Parts 210 and 211.
- Communicated and worked alongside various departments such as Production Management, Quality Assurance, Maintenance and Engineering staff, pertaining to the status of manufacturing operations, equipment reliability, environmental problems and potential quality and compliance concerns.
- Demonstrated strong attention to detail and organizational skills while performing a variety of production-related tasks.
- Executed manufacturing processes for the given area with strict adherence to GMP regulations, guidelines and safety procedures.
Education
High School Diploma -
Goldsboro High School
Goldsboro, NC06.1999
Skills
- Leadership, Staff Training, Lean Concepts, Pharmaceutical Manufacturing, Quality Control, Training Program Development, Production Protocols, Aseptic Technique, Production Maintenance, OSHA Compliance, cGMP, Quality Compliance, Regulatory Compliance, Production Efficiency, Formulation Analysis, Cross-Functional Collaboration, Technical Documentation
Timeline
ASEPTIC TECHNICIAN II
Pfizer
03.2020 - 07.2025
Formulation Technician
Pfizer
08.2015 - 03.2020
FILLING TECHNICIAN AND FORMULATION
Hospira, a Pfizer Company
03.2009 - 08.2015
High School Diploma -
Goldsboro High School