Technical Support Officer

• Writing GMP documents; protocols, reports, SOPs, BMRs and other technical or scientific documents.
• Responding to product queries from health authorities.
• Investigating and writing deviations or non-conformance reports and root cause analyses.
• Performing and writing risk assessments.
• Supporting new product introductions, writing documents, and performing practical formulation activities.
• Involvement in audits or inspections both from internal and external parties.
• Supporting validation activities as required.
• Managing small projects.

To be successful in this role, applicants need to have the following essential skills and experience:

• 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.

Desirable Skills and Experience

• Experience of implementing GMP or efficiency improvements.
• Problem solving experience., Do you want to feel inspired every day? We are future-focused, and our business is growing rapidly. We succeed together through passion, commitment, and teamwork, and so can you.

Due to continued growth, Reacta Healthcare is looking to recruit a Technical Support Officer who will provide technical and scientific support to all areas of the business. The role sits within the Technical & Validation team and reports to the Head of Technical & Validation.