C

Curia

End-to-end drug development and manufacturing

CSV Systems Engineer 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAlbany, NY, USAIn-person

About the Job

Requirements

  • A bachelor's degree in Information Technology or a related field is required.
  • At least 3 years of experience in quality and computer systems validation and/or information technology is required.

Responsibilities

  • Manage multiple site and global computer systems validation projects concurrently.
  • Maintain close communication with stakeholders and team members about computerized system needs, impacts on computer validation, project validation status, and other relevant issues.
  • Create all computer systems validation deliverables for computer systems validation projects.
  • Provide expertise in standard operating procedure generation and computer systems validation processes.
  • Own general configuration modifications to computer systems validation systems based on computer systems validation compliance standards.
  • Provide expertise in creating computer systems validation execution templates.
  • Perform computer systems validation risk assessments.
  • Own computer systems validation change records, corrective and preventive actions, and quality events for computer systems validation projects.
  • Act as the computer systems validation reviewer for defects and deviations within projects.
  • Support site and global computer systems validation actions arising from audits.
  • Participate in site audits and inspections as a computer systems validation subject matter expert.
  • Provide guidance and resolution on quality issues that affect data or system integrity.
  • Gather inventory and maintain scientific applications and computer systems across company sites, including good manufacturing practice and non-good manufacturing practice systems.
  • Inform Service Engineer I of changes in software and hardware status.
  • Support the Lab Ops team in ensuring computer systems have up-to-date antivirus software.
  • Support the Lab Ops team in ensuring computer systems have backup software installed.
  • Support the Lab Ops team in updating computer systems running outdated operating systems.
  • Perform monthly patching audit risk assessments with the Lead CSV Compliance Analyst.
  • Execute periodic reviews and data collection in preparation for internal audits and inspections.
  • Provide routine project status reports.
  • Provide routine software and hardware inventory updates.
  • Provide routine progress updates on standard operating procedures and templates.
  • Provide corrective and preventive action, quality event, and change record updates to the compliance team.
  • Provide routine audit observations and remediation updates.

Desired Qualifications

  • Experience in the pharmaceutical industry is preferred.

About the Company

Curia

End-to-end drug development and manufacturing

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Albany, NY
Founded
1991

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