Summary
Overview
Work History
Education
Skills
Timeline
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Patrick Sheridan

Brookline,NH

Summary

Highly-motivated employee with desire to take on new challenges. Strong work ethic, adaptability and exceptional interpersonal skills. Adept at working effectively, unsupervised and quickly mastering new skills. Offering 5+ years supporting GMP manufacturing mRNA and LNP operationss. Successful working long hours and shift changes in challenging environments to meet / exceed production timelines. Excellent history of working well with other team members and pitching in to help achieve team goals. Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy.

Overview

7
7
years of professional experience

Work History

Senior Manufacturing Associate

Moderna Therapeutics
12.2024 - 07.2025
  • Lead team members efforts through design, technical producibility, manufacturing reviews, and solutions creation.
  • Worked flexible hours across night, weekend and holiday shifts.
  • Daily downstream operations to meet production requirements and hit target commerical and clinical drug product quotas.
  • Batch generation, batch closeout, deviation writing, document control, SOP revisions.
  • Cross trained in additional manufacturing departments, regularly required to switch between these job functions.
  • Trained current and new employees on safe and efficient production procedures including; on-the-job trainings, clean room gowning procedures, aseptic technique, software seminars and good documentation practices.

Project Resilience

Moderna Therapeutics
Melbourne
08.2024 - 12.2024
  • Traveled to Melbourne, AUS for site opening and training development.
  • Created training techniques for global mRNA therapeutic teams.
  • Served as sole mRNA expert in country for approximately eight weeks.

Lead, Clinical Manufacturing Associate II

Moderna Therapeutics
09.2022 - 12.2024
  • Streamlined production processes through collaboration while adhering to safety protocols.
  • Escalated manufacturing issues to management and quality assurance for prompt resolution.
  • Contributed to updates for SOPs, continuous improvement initiatives, CAPAs, and change controls.
  • Operated production equipment to manufacture mRNA-based therapeutics efficiently.

Manufacturing Associate

Moderna Therapeutics
08.2020 - 09.2022
  • Met production targets and tight deadlines by collaborating closely with team members.
  • Used problem-solving and issue-resolution skills to promptly and successfully address production problems.
  • Collaborated with other departments to optimize production workflows.
  • Prepared reports and technical documentation of day-to-day production processes.

QA Component Inspector

Azurity Pharmaceuticals
05.2020 - 08.2020
  • Raw material visual inspection, validation, documentation and review for accuracy and quality before release to manufacturing.
  • Solving documentation related issues, which were not limited to, batch closeout, deviations, manufacturing protocols, purchase orders, process orders and training documents.
  • Reported repeated issues to supervisors and other departments, collaborating to identify issue roots and rectify problems.

QA Metallurgy Lab Technician

Hitchiner Manufacturing
10.2019 - 04.2020
  • Real-time elemental composition adjustments, based on specifications for a given custom orders.
  • Spectrometry, x-ray fluorescence, physical and wet chemistry techniques on nickel superalloy material.
  • Developed QA testing procedures and verified performance of tests according to established item specifications and protocol.
  • Completed supporting documentation for testing procedures, data capture forms, equipment logbooks and inventory forms.
  • Documented and executed detailed test plans and test cases and summarized and logged audit findings for reporting purposes.

R&D Lab Technician

Klüber Lubrication
09.2018 - 06.2019
  • Self-motivated, with a strong sense of personal responsibility.
  • Skilled at working independently and collaboratively in a team environment.
  • Daily R&D testing protocols, lab management which include, data entry, inventory and weekly ordering, internal and external sample preparation, equipment cleaning, maintenance and record keeping
  • Aided a 2->200kg scale up process to develop custom oil/grease products for aerospace and automotive industries.

QC Medical Device Lab Associate

Getinge
01.2019 - 05.2019
  • Inspection and destructive testing of medical devices to meet quality specifications.
  • Strict adherence with cleanroom gowning procedures, cleanroom gowning technique and behavior, aseptic technique.
  • Maintained safe, tidy and organized laboratory environment for accurate test results.
  • Regularly worked independently and in a small team to achieve time sensitive sample collection, and to meet a total tested quota per day.

Education

Some College (No Degree) - Chemistry

University of Massachusetts
Lowell, MA

Skills

  • Aseptic Technique
  • JMP and SPSS
  • Affinity Chromatography
  • Reverse-Phase Chromatography
  • ISO Class 7 Cleanroom Operation
  • Grade C and Grade D Cleanrooms
  • Manufacturing Execution Systems
  • SDS-PAGE
  • Spectrophotometry
  • Corrective and Preventative Action
  • Microsoft Office Proficient
  • cGMP Documentation and GDP
  • SAP, DeltaV, Syncade
  • Unicorn AKTA Systems
  • Millipore Tangential Flow Filtration

Timeline

Senior Manufacturing Associate

Moderna Therapeutics
12.2024 - 07.2025

Project Resilience

Moderna Therapeutics
08.2024 - 12.2024

Lead, Clinical Manufacturing Associate II

Moderna Therapeutics
09.2022 - 12.2024

Manufacturing Associate

Moderna Therapeutics
08.2020 - 09.2022

QA Component Inspector

Azurity Pharmaceuticals
05.2020 - 08.2020

QA Metallurgy Lab Technician

Hitchiner Manufacturing
10.2019 - 04.2020

QC Medical Device Lab Associate

Getinge
01.2019 - 05.2019

R&D Lab Technician

Klüber Lubrication
09.2018 - 06.2019

Some College (No Degree) - Chemistry

University of Massachusetts
Patrick Sheridan