To provide a quality support to the Quality Systems, Operational Quality and Technical Quality teams as required.

Provide Quality Operations support to the warehouse, primary and secondary packing and laboratory areas as required.
Review pharmaceutical product batch files for timely release by Responsible Person (RP) or certification by Qualified Person (QP).
Provide QA support to the business during root cause analysis investigation
Raise in a timely manner on request or using own initiative Third party notification, CAPA, Deviation and Change Control.
Support activities required to effectively maintain the company Pharmaceutical Quality System
Monitor alerts for potential overdues for Complaints, CAPA, Deviation and Change Control.
Other duties as assigned

Demonstrate flexibility and willingness to support
Ability to work effectively as part of a team
Be punctual, polite and courteous
Ability to use initiative
Good communication skills

Graduate in Pharmaceutical Science or equivalent
Lead auditor trained
Educated to A-level standard in scientific subjects

Experience & Competencies
Previous experience working in QA, QC or Production with in a GMP environment
Previous experience working in a similar role within a Pharmaceutical company
Previous experience creating of updating policies and procedures
Experience of solid dosage forms, liquids, creams and sterile products
Full, valid UK driving licence

Knowledge & Skills
Excellent communication skills, both written and oral
Good working knowledge of Good Manufacturing Practice, Standard Operating Procedures, MHRA guidelines and ICH Guidelines
Knowledge of Sage ERP (Waymade Stock Control Programme)
IT literate in Microsoft Software Packages, particularly Word, Excel and Outlook

Personal Qualities
Enthusiastic and highly motivated
Positive attitude and flexible approach to work.
Self-starting and able to work on own initiative
Reliable and punctual
Strong attention to detail

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