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MedPharm

Topical and transdermal drug delivery CDMO

IT Operations & Scientific Systems Specialist

System Administration +1Confirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • Bachelor’s degree or equivalent practical experience in Information Technology, Computer Science, a scientific discipline, or a related field.
  • At least 5 years of hands-on IT support or systems administration experience, including at least 3 years supporting laboratory, manufacturing, or other regulated environments.
  • Working knowledge of GxP and 21 CFR Part 11 requirements, change control, and data integrity principles.
  • Proficiency with Windows 10/11, Active Directory, and Microsoft 365 administration; familiarity with Windows Server.
  • Experience supporting instrument-connected PCs and scientific software in a laboratory setting.
  • Familiarity with PC imaging, backup solutions, NAS administration, and virtualization.
  • Working understanding of networking fundamentals, including TCP/IP, DNS, DHCP, VLANs, and Wi-Fi.
  • Strong documentation skills, including experience writing or executing SOPs, test scripts, or change controls.
  • Ability to travel locally between the Stirrup Creek and Emperor Blvd sites as needed; personal or company vehicle required.
  • Professionalism and discretion when handling confidential data and sensitive systems.
  • Ability to follow gowning, PPE, and safety procedures in regulated laboratory environments; occasional lifting and moving of IT equipment is required.

Responsibilities

  • Provide Tier 1–2 deskside, phone, and ticket-based troubleshooting for hardware, software, and enterprise applications across the Stirrup Creek and Emperor Blvd sites, resolving issues within defined service levels.
  • Image, deploy, patch, maintain, and retire desktops, laptops, mobile devices, and related peripherals, and maintain accurate hardware and software asset records.
  • Administer user accounts in Active Directory and Microsoft 365, including onboarding and offboarding, group and distribution list management, licensing, and multi-factor authentication, in partnership with HR.
  • Ensure Microsoft updates are applied to endpoints and servers in a timely and controlled manner.
  • Use remote control tools to support desktop and software issues.
  • Support printers, phones, conference-room and audio-visual equipment, perform first-line troubleshooting of wired, Wi-Fi, and VPN connectivity, and escalate issues as appropriate.
  • Assist with server, VMware virtualization, and Veeam backup operations, including job monitoring and restore requests.
  • Reinforce security best practices with end users, including phishing awareness, device encryption, and acceptable use.
  • Install, configure, and support PCs and software that control laboratory instruments, including HPLC/UPLC, GC, dissolution and diffusion systems, FTIR, Karl-Fischer equipment, microscopes, titrators, and spectrophotometers.
  • Administer Chromatography Data Systems, including Waters Empower, encompassing user and role management, system configuration, LAC/E support, and instrument integration.
  • Own backup, restore, and archiving processes for instrument and scientific data, including Synology and QNAP NAS devices, and perform and document periodic restore tests to verify recoverability.
  • Maintain secure configuration of laboratory devices, including network placement, antivirus settings and exclusions, and operating system hardening of instrument workstations.
  • Coordinate patching and operating system upgrades on validated instrument PCs through formal change control, working with instrument vendors, laboratory personnel, and QA.
  • Serve as the day-to-day IT point of contact for laboratory staff and instrument service engineers during installations, upgrades, repairs, and relocations.
  • Maintain validated states for computerized systems in compliance with GxP and 21 CFR Part 11 requirements and ALCOA+ data integrity principles.
  • Author, update, and maintain SOPs, work instructions, and change control records; participate in deviations, investigations, and CAPAs related to IT systems.
  • Support validation activities, including drafting and executing IQ/OQ protocols and test scripts for IT systems and laboratory informatics platforms.
  • Perform periodic user access reviews and support audit trail reviews and periodic system reviews in collaboration with QA.
  • Support internal, client, and regulatory audits by providing evidence of IT controls and system documentation.
  • Collaborate with the Manager, GxP Systems and Site Operations, Vice President of IT, UK Site Lead, IT contractors, and cross-functional teams including QA, Laboratory, Manufacturing, and Operations.
  • Coordinate with external IT and instrument vendors for system upgrades, preventive maintenance, and issue resolution.
  • Participate in special projects, on-call duty rotation, and strategic IT initiatives as required.
  • Travel between the Stirrup Creek and Emperor Blvd sites as needed to deliver consistent IT support across both locations.

Desired Qualifications

  • Experience with Chromatography Data Systems, preferably Waters Empower.
  • Pharmaceutical, biotech, or CDMO experience.
  • Relevant certifications such as CompTIA A+, Network+, Security+, Microsoft 365, or ITIL Foundation.

About the Company

MedPharm

Topical and transdermal drug delivery CDMO

MedPharm is a contract development and manufacturing organization focused on topical, transdermal, and mucosal drug delivery. It provides end-to-end services from formulation development through clinical and commercial manufacturing, including analytical testing and regulatory support, and operates proprietary delivery platforms such as MedSpray, MedTherm, and AquaRMed to enable multiple administration routes. The company combines contract research with a patent portfolio and offers lifecycle support across development and manufacturing, differentiating itself from competitors. A July 2024 merger with Tergus Pharma expanded capabilities to include hormone-based and highly potent drugs, enhancing scale and scope with the aim of helping pharma and biotech move products from early formulation to scalable manufacturing.

Company size
Not listed
Company stage
Grant
Total funding
$390K
Headquarters
Guildford, United Kingdom
Founded
1999

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