CSV Engineer
Posted 1 week ago by Impact Engineering
Negotiable
Undetermined
Undetermined
Craigavon, Northern Ireland, United Kingdom
Summary: The CSV Engineer role at Impact Engineering Ltd involves providing project support for a key pharmaceutical customer in Northern Ireland. The position requires collaboration with the CSV Lead to ensure compliance with protocols and regulations while adhering to GMP requirements. Candidates must have relevant experience in life sciences and automation projects. Sponsorship is not available for this position.
Key Responsibilities:
- Work closely with and follow the instructions of the CSV Lead to ensure compliance with required protocols and regulations.
- Perform all duties in accordance with GMP requirements, SOPs and controlled documents.
- Support the project team as they work towards execution and handover.
Key Skills:
- 3+ years experience in life sciences.
- Knowledge and illustrated experience of working with GAMP, 21 CFR Part 11, etc.
- Excellent ability to work with others showcasing strong communication and organisational skills.
- Prior experience of working in automation projects is preferred.
Salary (Rate): undetermined
City: Craigavon
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Company Description Impact Engineering Ltd is a trusted automation partner focused on business transformation, digitalization, and providing innovative automation solutions. Our mission is to maximize safety, quality, and efficiency while minimizing costs and environmental impact. We offer a range of services from consultancy to automation projects and targeted training, all aimed at adding value to businesses navigating digitalization.
About the Role: We are seeking to hire a CSV Engineer to join the Impact Engineering team providing project support for a key pharmaceutical customer in Northern Ireland. Candidates must be approved to work in Ireland or United Kingdom. Candidates requiring sponsorship cannot be considered at this time.
Responsibilities:
- Work closely with and follow the instructions of the CSV Lead to ensure compliance with required protocols and regulations
- Perform all duties in accordance with GMP requirements, SOPs and controlled documents.
- Support the project team as they work towards execution and handover
Requirements:
- 3+ years experience of life sciences experience
- Knowledge and illustrated experience of working with GAMP, 21 CFR Part11 etc.
- Excellent ability to work with others showcasing strong communication and organisational skills
- Prior experience of working in automation projects is preferred