Data Validation and Support Specialist

Key Responsibilities Areas

• The key responsibility areas (KRAs) are major outputs for which the position is responsible and not a comprehensive statement of all position activities.

Information Systems

• Be actively involved in performing Computer Systems Validation activities, particularly with spreadsheets validation as according to the spreadsheet validation SOP.
• Create, update and/or review validation documents including but not limited to spreadsheet/user requirements, test plans, IQ/OQ/PQ tests, UAT and reports
• Writing and reviewing validation documentation that meet regulations and requirements, including change management activities
• Facilitate and conduct functional risk assessments
• Liaise with stakeholders (vendors, subject matter experts, testers) in the planning and execution of CSV projects
  • Includes prospective, concurrent and retrospective validation
  • Includes spreadsheet validation
  • Where required, prepare spreadsheet templates and validate their use according to SOP.
  • Review spreadsheet templates if prepared by others and assist in validating their use
  • Be involved in maintaining validation of computerised systems and spreadsheets
  • Assist in maintaining Computer Systems Validation SOPs and Templates
  • Must be highly proficient with the use of Excel, particularly with formulas, functions and protecting spreadsheets
  • Provide application support for a wide range of scientific applications. This includes covering the entire lifecycle of application systems, from strategy through to support and retirement
  • Be involved in investigating, analysing hardware and software problems, and ensuring relevant validation documentation are updated
  • Contribute towards scientific system upgrades, installation, integration, customisation and configuration, and ensure validation documents are updated accordingly
  • Maintain effective communication with users when resolving incidents and fulfilling requests
  Accreditation
  • Adhere to ISO/IEC 17025, OECD Principles of GLP, GCLP Principles, 360biolabs’ Quality Management System, and other requirements as relevant per NATA Accreditation and regulatory guidelines.
  Team Work
  • Maintain high levels of communication with colleagues
  • Collaborate well in a cross functional matrix environment
  Safety
  • Ensure the safe and efficient conduct of company activities
  • Ensure compliance to relevant internal processes and statutory requirements
  Professional Development
  • Attend meetings associated with Information Systems or the work of 360biolabs
  • Participate in professional activities including attendance at training courses and seminars in the field of expertise

Key Selection Criteria

Qualifications

• Degree in Science or IT or equivalent plus relevant experience (Essential)

Experience / Knowledge / Attributes
High degree of self-motivation with the ability to work independently and to effectively manage and prioritise work (Essential)
Eagerness to learn, be pro-active and willing to share knowledge (Essential)
Strong analytical and problem-solving skills; ability to perform root cause analysis (Essential)
Approachable individual that is dedicated to providing friendly support, as well as willing to go the extra mile (Essential)
Excellent administrative and organisational skills (Essential)
Experience in writing computer system test scripts, validation protocols and summary reports (Essential)
Experience in technical writing in both validation and QMS documentation (Essential)
Good interpersonal skills to facilitate interaction among staff and project teams (Essential)
Ability to work effectively as part of a multi-disciplinary team (Essential)
Excellent analytical, interpersonal, verbal and written communication skills (Essential)
High level of attention to detail (Essential)
Working knowledge of IT hardware and software, including Windows Server and Desktop OS (Essential)
Highly proficient with Microsoft Excel, particularly with formulas and functions (Essential)
Good understanding on version control with documents and spreadsheets (Essential)
Broad knowledge and exposure to computer systems validation principles and methodology, including quality guidelines and regulations (GxP) (Essential)
Good knowledge of regulations applicable to computerised systems (eg US FDA 21 CFR Part 11, GLP) (Essential)
Knowledge and exposure to systems such as LIMS and Document Management Systems (Desirable)
Experience with Excel macros and VBA (Desirable)
Knowledge and exposure to computerised systems validation (Desirable)
Basic knowledge of ‘good practise’ of quality guidelines and regulations (GxP) (Desirable)
Ability to work independently on multiple concurrent projects with minimal guidance (Desirable)
Experience working in a Scientific Environment (Pharma/Biotech) (Desirable)
Experience working with a range of scientific software (Desirable)