GxP Computer Systems Administrator

placeFramingham calendar_month 

Overview:

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.
Audacious: We Are Bold and Innovative.
Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients.

Join us, as we reshape the future.

Job Summary:

The GxP Computer Systems Administrator will be responsible for managing GxP-compliant and lab computer systems and ensuring their optimal performance. They will collaborate closely with various teams such as Validation, Quality, and Manufacturing to maintain the integrity of computer equipment connected to GxP systems.
Their primary objective will be to ensure that these systems remain operational, audit-ready, and function within regulatory and quality guidelines, supporting the company's mission to deliver high-quality and compliant biotechnological products.

This position will be located onsite in Framingham, MA, and will also need to be available to work with the UK teams remotely in the early mornings Eastern time.

This position is based in our Framingham location and typically has a 5-day on-site expectation.

Responsibilities:

Key responsibilities:

  • Build, manage, configure, and monitor GxP connected and lab computer systems, particularly on Windows OS, ensuring continuous uptime, security, and performance of systems connected to laboratory and manufacturing equipment.
  • Work within IT and QA Change Control systems to ensure the business is appropriately executing Change Controls on GxP and lab connected computer systems.
  • Maintain administrator access on GxP software and computer systems and ensure protocol is followed in granting system access to users.
  • Work closely with the Director, GxP and lab Applications and Sr. Mgr of IT Operations to create, maintain, and update all necessary GxP documentation to ensure systems are always audit-ready. Maintain SOPs, user manuals, forms, and device qualification.
  • Ensure that backup and system update operations for GxP and lab computer systems are executed to specification. Monitor and verify that backup and recovery processes are functioning as required and troubleshoot issues when necessary.
  • Assist the Validation, and Quality Assurance teams by assisting them in reviewing log data for potential errors, inconsistencies, or anomalies that could impact system integrity or compliance.
  • Act as the primary point of contact for identifying and resolving hardware and software issues related to GxP and lab connected computer systems. Provide hands-on support for diagnostics, patching, and system upgrades.
  • Work collaboratively with cross-functional teams including IT, Validation, Quality Assurance, Manufacturing, and Research & Development to support the integration and operation of GxP and lab computer systems.
Other responsibilities
  • Ensure GxP and lab computer systems are secure and adhere to the company’s Cybersecurity strategy.
  • Ensure compliance for technology projects including GDPR, Sarbanes Oxley, 201 CMR 17.00, 21 CFR Part 11and cGxP requirements.

Qualifications:

Education:

  • Bachelor’s degree in Computer Science, Information Technology or equivalent experience.

Required Experience:

  • 3-5 years experience working with GxP-compliant systems in a biotech, pharmaceutical, or medical device environment.
  • Strong knowledge of GxP, 21 CFR Part 11, and GAMP5 regulations
  • Experience working with audit trails, electronic record management systems and familiarity with FDA audits.
  • Expertise in Windows OS administration and Microsoft’s update cycle.
  • Familiarity with lab and manufacturing equipment used in biotech or pharmaceutical production environments.
  • Experience with backup management and data recovery.
  • Understanding of IT service management principles (ITIL framework is a plus).
  • Ability to troubleshoot hardware and software issues, perform system upgrades, and ensure robust security measures.
  • Excellent documentation and communication skills with a high attention to detail.
  • Ability to work effectively in a fast-paced, regulated environment and manage multiple priorities.

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response.
The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.

The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.

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