Cranleigh Scientific
QA Officer - 12 Month Contract
Job Location
Englefield, United Kingdom
Job Description
A diagnostics manufacturer has an exciting 12 Month Contract for a QA Officer to join the team. The main purpose of the role will be to ensure compliance within the Quality Management System (QMS). You must have previous experience in an ISO9001 compliant QA function.
RESPONSIBILITIES
•Work closely with the QA/RA Manager managing the Quality Management System.
•Assist all quality and regulatory projects, processes, and activities
•Reviewing and approval of QA-controlled documentation (such as SOPs, batch records, working instructions, non-conforming work);
•Support for the development of appropriate Corrective and Preventative Actions (CAPAs) and continuous improvement activities.
•Maintenance of training records matrices for relevant staff
•To provide administrative support to the QA/RA department and any other duties as requested
•Assist in regulatory audits i.e., ISO9001
•Lead on internal audits
•Act as point of contact for Manager for QA related tasks when QA/RA Manager is not on site
QUALIFICATIONS
Educated to A levels standard.
Degree in Life Sciences (related subject) desirable but not essential
At least 2 years’ experience in a QA regulated environment, industry or science-based company desirable but training will be provided.
Understanding and knowledge of Quality Management Systems (QMS)
Good communication and interpersonal skills
Ability to work proactively both individually and as part of a team
Strong statistical data analysis skills
Ability to be methodical, conscientious, organized and show attention to detail
To maintain a high level of integrity, motivation, and reliability in all work
To be decisive where needed, display decision making and problem-solving skills
Computer literate
Attention to detail
Time management skills
Hybrid: 1-2 days from home after probation
Location: Englefield, GB
Posted Date: 11/24/2024
RESPONSIBILITIES
•Work closely with the QA/RA Manager managing the Quality Management System.
•Assist all quality and regulatory projects, processes, and activities
•Reviewing and approval of QA-controlled documentation (such as SOPs, batch records, working instructions, non-conforming work);
•Support for the development of appropriate Corrective and Preventative Actions (CAPAs) and continuous improvement activities.
•Maintenance of training records matrices for relevant staff
•To provide administrative support to the QA/RA department and any other duties as requested
•Assist in regulatory audits i.e., ISO9001
•Lead on internal audits
•Act as point of contact for Manager for QA related tasks when QA/RA Manager is not on site
QUALIFICATIONS
Educated to A levels standard.
Degree in Life Sciences (related subject) desirable but not essential
At least 2 years’ experience in a QA regulated environment, industry or science-based company desirable but training will be provided.
Understanding and knowledge of Quality Management Systems (QMS)
Good communication and interpersonal skills
Ability to work proactively both individually and as part of a team
Strong statistical data analysis skills
Ability to be methodical, conscientious, organized and show attention to detail
To maintain a high level of integrity, motivation, and reliability in all work
To be decisive where needed, display decision making and problem-solving skills
Computer literate
Attention to detail
Time management skills
Hybrid: 1-2 days from home after probation
Location: Englefield, GB
Posted Date: 11/24/2024
Contact Information
| Contact | Human Resources Cranleigh Scientific |
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