Planet Pharma
Quality Information System Analyst (FTC)
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Join Our Team as a Quality Information System Analyst – Be a Key Player in Our Digital Transformation!
Are you passionate about leveraging technology to optimise quality systems within a dynamic pharmaceutical manufacturing environment? We are seeking a talented and motivated Quality Information System Analyst to support our journey towards smarter, integrated, and automated operations. This pivotal role offers the chance to contribute directly to groundbreaking initiatives that impact patients worldwide, working within a collaborative team committed to excellence and innovation.
What You’ll Do
- Support the implementation, maintenance, and continuous improvement of GMP-compliant IT systems, focusing on Quality Systems such as LIMS, CDS, and Quality Control Equipment Applications.
- Collaborate with manufacturing, IT teams, and third-party vendors to resolve technical issues, deliver system upgrades, and optimise processes.
- Lead validation activities, author validation documentation, and ensure data integrity in line with regulatory standards.
- Facilitate change management processes, handle IT requests via ticketing systems, and support audits and inspections related to IT quality and compliance.
- Contribute to project planning, requirements gathering, system design, testing, and deployment of new IT solutions aligned with business needs.
- Drive continuous improvement by evaluating processes, recommending enhancements, and staying current with industry trends and regulatory changes.
- Support the organisation’s smart factory initiatives, working across teams to implement innovative solutions.
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Essential Skills & Qualifications
- Bachelor’s degree in Computer Science, Information Systems, or a related field, or equivalent work experience in a regulated environment.
- Proven experience supporting pharmaceutical quality and manufacturing systems, with hands-on expertise in LIMS, CDS, and GMP-regulated quality systems.
- Strong knowledge of System Lifecycle Management, Computer Systems Validation (CSV), and GAMP5 methodologies.
- ITILv4 certification or equivalent experience.
- Familiarity with SQL, data management, analytics, and project management tools.
- Experience supporting validation, change control, and audit readiness within a regulated environment.
- Excellent communication skills, with the ability to simplify technical concepts for non-technical stakeholders.
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Nice To Have Skills
- Knowledge of pharmaceutical laboratory and quality management systems.
- Experience with Agile methodologies and software development lifecycle.
- Understanding of cybersecurity best practices in a manufacturing setting.
- Project management experience.
- Familiarity with GMP standards and regulatory frameworks specific to the pharmaceutical industry.
Preferred Education & Experience
- A relevant degree or equivalent professional experience supporting GMP-regulated systems.
- Prior experience in a pharmaceutical or biotech manufacturing environment.
- Demonstrable expertise in supporting and validating complex IT systems within regulated industries.
Take the next step in your career by joining a forward-thinking organisation dedicated to innovation and quality. Apply now to be part of our transformative journey toward smarter manufacturing—your expertise can make a real difference!
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