Technical Support Officer
$30,000–$35,000 year
On-siteDeeside, Wales, United Kingdom
Job Summary
Write GMP documents including protocols, reports, SOPs, BMRs, and technical or scientific documentation. Respond to product queries from health authorities and investigate deviations or non-conformance reports to write root cause analyses. Perform risk assessments, support new product introductions with practical formulation activities, and manage small projects. Participate in internal and external audits or inspections and support validation activities as required. This role sits within the Technical & Validation team at Reacta Healthcare, a future-focused pharmaceutical business growing rapidly.
Required Qualifications
- Degree or similar in scientific or technical discipline
- Experience of working within a pharmaceutical or related GMP environment
- Demonstrated written and oral communication skills
- Demonstrated ability to work well as part of a team
- Experience of IT software (e.g., Microsoft office, document management or other relevant software)
- Has worked in a technical or scientific role
- Demonstrated planning/organisational skills and the ability to work under their own initiative
Desired Qualifications
- Experience of implementing GMP or efficiency improvements
- Problem solving experience
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