What are the responsibilities and job description for the 9265 - Quality Analyst II position at Orion?
Job description
Orion Group Life Sciences are looking for a Quality Analyst II for our Pharmaceutical client based in Runcorn. Initial 12-month. Hybrid role, 70% onsite and 30% from home.
Purpose of the role
- Author of qualification documents for Quality control department equipment's. (Examples, CSV, VP, FDS, URS, etc).
- Writing the protocols required for qualification documents such as IOQP etc.
- Coordinating with CSV, QA and IT team and external vendor for execution of the qualifications.
- Writing user SOP's for the equipment's with in the Quality Control department.
- Project plan and attending the regular meeting with in the department.
Required skills and knowledge
- Science degree or equivalent.
- Good planning skills.
- Good organisational skills.
- Good Communication skill.
- Understanding of GMP, CFR21 and Data integrity.
- Good attention to detail.
If you would like to have a confidential conversation regarding this opportunity please reach out to Tim Browaeys, tim.browaeys@orioneng.com or contact Tim on 0044 7593448607
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Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
