eCSV Compliance Advisor

KeyResponsibilities:

The CSV Analyst will supportGxPimpactingprojects to ensure that all applicable regulatory and compliance requirements are met for any new or revised computerized systems to ensure that these systems are not only defendable during aninspection, butalso confirm that the delivered systems/services are fit for purpose by meeting user requirements.Your Contributions (include, but are not limited to):

Implementation Projects

• Evaluate proposed new computerized systems or software to assessGxPimpact and whereGxPimpact isidentifiedprovides guidance on the risk-based validation approach for the system

• Work closely with the Project manager to ensure all compliance milestones are met during the project lifecycle

• Assistin the development of validation deliverables including Validation Plans, Test Plans/Protocols/Scripts, Specifications and Design Documents, Compliance Assessments, Risk Assessments, Installation Qualification, System and User Acceptance Testing, Data Migration Plans, Traceability Matrices, Validation Reports, Supplier Assessments, etc.

• Prepare, or review and approve major system documentation to ensure consistency with quality standards and quality of deliverables

• Establish andmaintainstandards and training materials for the specification, design, development, configuration, implementation, validation,useand maintenance ofcomputerized systems which support the development,manufactureand distribution of products in alignment with applicable companypolicies and regulations

• Coach the implementation teams in the proper execution of validation documents

• Manage formal testing of computerized systems including, setup of testing, documentation, approval, delivery, and test reporting

• Solve problems during validation process and address/advise onissues such as deficiencies, deviations, and change controls. Ensure initiation/preparation and closeout of all CSV related deviations.

• SupplyaccurateKPIs to management on Project compliance status

   

System Maintenance

• Review proposed changes tovalidatedcomputer systems/qualified IT infrastructure andidentifythe validation or qualification requirements necessary tomaintainthe validated/qualified state after execution of the change

• Ensure all changes are implemented and documented in a compliant manner

• Perform periodic assessment to review and confirm validated status

• Perform periodic re-validations

Quality Management

• Ensure initiation/preparation and closeout of all CSV related deviations, discrepancies and change control documents

• Conduct Quality Reviews to evaluate if processes and deliverables fulfil the requirements for quality, to uncover errors or deficiencies in processes and deliverables, and toidentifystrengths and opportunities for improvement

• Follow up resolution ofidentifiedquality exposures and escalation to team lead if critical situations are not resolvedin due course

• Ensure that suppliers of IT services and solutions areproperly assessedtodeterminetheir level of competence and reliability, and ensure the organization employs appropriaterisk basedapproaches to deliverytaking into accountthe output of the supplier assessment

• Maintain up to date knowledge of evolving regulatory requirements, availability of current/new techniques, and literatureregardingcompliant computer systems, and acts as an information resource for the delivery teams and wider business

 Other

• To ensure compliance with the legislative and internal requirements of the EHS and toparticipatein the fulfillment of the company's targets in the EHS area

Authority (ifapplicable):

• Project decisions that fall under Computerized Systems Validation internal or external guideline will be taken by the CSV Manager

• Approve CSA documents that have a role CSV Manager / CSV Analyst / ITQA approval

Skills & Experience:

• Strong understanding of GXPRegulatationsand best practice (21CFR820, 21CFR11, Annex 11,GAMP, etc.)

• Demonstrated experience in successfully managing complex validation projects andmaintainingthe validation requirements for computerized systems supporting healthcare products

• Detailed understanding of computer system validation and infrastructure qualification, including the application of risk managed approaches

• Experience in electronic software applications such as Electronic Document Management System (EDMS), Product Lifecycle Management (PLM), Quality Management Systems (eQMS), Complaint Management Systems, Enterprise Resource Planningsystems(ERP), etc.

• Ability to rapidly adapt to new situations and environments

• Excellent communication skills with the ability to effectively convey compliance requirements at all levels

• Ability to influence, negotiate, and constructively challenge to achieve productive solutions

• Ability to handle a high concentration of work through successful multitasking & prioritizing

• Conscientious and highly committed, with a dedication to quality

Qualifications/Education:

- Bachelor’s/other degreein computer science, engineering lifescienceor related field, plus 2years experiencewith CSV validation lifecycle management, validation documentation development.

- 2 plus years pharmaceutical manufacturing or Medical Device industry experience in computer systems validation, process validation,QAor compliance functions.

- Excellent understanding and experience with industry regulations, standards, and guidelines, e.g.,GxP, validation, 21 CFR Part 11, etc.

- Excellent presentation and writing skills.

Preferredtrainingrequirements:

• Quality System documents and procedures relevant to all employees (local and Convatec corporatee.g.Code of Ethics and Business Conduct, Quality Policy, Complaints,relevantGxPdocuments), including regular re-training whenrequired

• Quality System documents and procedures relevant to job performance

Occasional on‑site presence may be required for hands‑on validation activities on the machines, depending on business needs.

Note: Please send your CV only in English language.