Summary
Overview
Work History
Education
Skills
Timeline
Generic

Melissa Snowden

Weymouth,MA

Summary

Detail-oriented and hard-working operator with 4 years of experience in GMP-regulated pharmaceutical positions.

Overview

7
7
years of professional experience

Work History

Senior Manufacturing Technician

Sanofi
Framingham, MA
09.2025 - Current
  • Conducted Downstream Purification operations for two drug products, working with SUT (single-use technology) items, purification skids, nanofiltration, and other equipment used in the process.
  • Adhered to safety protocols and quality standards in all manufacturing processes.
  • Assisted in troubleshooting equipment malfunctions and implemented corrective actions.
  • Collaborated with team members and other departments to ensure workflow efficiency.

Manufacturing Associate/Team Leader

Catalent Pharma Solutions
Chelsea, MA
09.2023 - 09.2025
  • Operate industrial spray drying equipment and other manufacturing equipment units such as autoclaves, parts washers, and filter integrity testing machinery. Monitor production parameters on an HMI and make adjustments and conduct needed tasks as necessary during the batching process.
  • Ramp up and ramp down spray dryer production for each batch and complete COP cleanings of parts used and ready everything for the next production batch. Document, verify and review activities in GMP regulation logbooks and batch records. Assemble, disassemble, setup, and conduct CIP procedures on spray dryer equipment and IBCs used in production.
  • Follow SOPs, OJT, gowning, and safety requirements. Follow GMP and GDP regulations. Maintain clear communication with team and other departments, including composing shift notes at the end of the day and attending meetings.
  • Act as a team lead to guide and direct the team.

Senior Manufacturing Technician

Sanofi
Framingham, MA
03.2022 - 09.2023
  • Processed equipment parts and batched cell media used for biopharmaceutical manufacturing.
  • Created and executed electronic batch records via PAS-X MES; also utilized paper logbook records.
  • Operated autoclaves, scales, industrial parts washers, CIP/COP, conductivity and pH meters, media batching, sampling, aseptic technique, visual inspection, equipment assembly, batching caustic solutions/soak tanks, and filter integrity testing.
  • Followed SOPs, gowning, and safety requirements. Communicated with other departments such as QA and facilities. Conducted monthly and special manufacturing equipment disinfections.

Supervisor

Cleanroom Facility Services
Framingham, MA
07.2019 - 03.2022
  • Trained and managed a crew for the process of nightly aseptic technique disinfections and GDP-adhered logbook documentation in a biopharmaceutical manufacturing controlled environment (Sanofi Framingham).
  • Ensured completion of disinfection procedure, activity documentation, overseeing document corrections, document review, action notice special disinfection execution and documentation. Communicated with other departments.
  • Followed SOPs. Gowning procedure. Participated in Sanofi iLearn learning modules.

Education

Associate of Science - Biology

Quincy College
Quincy, MA
05-2023

Associate of Science - Healthcare Administration

Quincy College
Quincy, MA
05-2019

Skills

    Fast Learner; Retains Information Well

    Attention to Detail

    Interpersonal and Writing Skills

    Ability to Work Independently or as a Team Player

    Hard-Working and Reliable

    Experience in supervising a team

    Computer literate/MS Office

    GMP and GDP Experience

Timeline

Senior Manufacturing Technician

Sanofi
09.2025 - Current

Manufacturing Associate/Team Leader

Catalent Pharma Solutions
09.2023 - 09.2025

Senior Manufacturing Technician

Sanofi
03.2022 - 09.2023

Supervisor

Cleanroom Facility Services
07.2019 - 03.2022

Associate of Science - Biology

Quincy College

Associate of Science - Healthcare Administration

Quincy College
Melissa Snowden