International Pharmaceutical Manufacturer seeks an experienced QA Officer.
Participate in daily updates for batch release priority.
To initiate and assist with deviations and changes related to batch review and be able to assess them on behalf of the QP.
Complete GMP reviews of batch documents in a timely manner in keeping with manufacturing schedules.
Highlight significant GMP and patient safety concerns to supervisor or QP’ as needed.
To co-ordinate and maintain the files for a range of quality records as required
To participate as required in Regulatory and customer audits.
To assist in progression of regulatory actions, customer complaints, GDP incidents where required.
To perform regular audits of the manufacturing facility and contribute to continuous improvement activities
To undertake work related to job objectives as directed by QA management.Skills and experience
Degree level qualification in science discipline or equivalent.
Experience of working within a (bio) pharmaceutical, clean room or manufacturing environment.
Knowledge of sterile aseptic filling and packing manufacturing processes is desirable.
The job holder is expected to demonstrate a willingness to engage in self-directed learning, an ability to assimilate new information into their routine working practices and a desire to develop their level of experience and expertise.
Experience of working with documentation and quality management systems desirable.
A natural tendency towards continuous improvement is required.
Job Type: Permanent
To apply for this job please visit www.cv-library.co.uk.