Company: Skills Alliance
Location: East Midlands
Closing Date: 28 Feb 17
Salary (£): 60,000 - 80,000
Benefits: bonus and extensive benefits package
QP / Qualified Person and Quality Technical Support Manager – Large, Global Healthcare Brand – East MidlandsSkills Alliance have partnered with world-leading healthcare company based /...
QP / Qualified Person and Quality Technical Support Manager – Large, Global Healthcare Brand – East Midlands
Skills Alliance have partnered with world-leading healthcare company based in East Midlands for the appointment of a QP / Qualified Person who, alongside batch release of a variety of dosage forms will also act as the technical SME within Quality on various projects across the site.
Based on a busy manufacturing site that develops (R&D) and manufactures a huge variety of products covering almost every dosage form including Steriles and non-Steriles. As a diverse site with fluid changes to manufacturing capabilities there is a consistent need for technical input from the Quality department as new product lines and manufacturing suites are added.
As QP you will be responsible for compliant batch release of IMP and Commercial products covering a variety of dosage forms within a busy manufacturing environment. Contributing to high-profile projects as the Quality Technical SME; completing risk assessment, advising on Technical/Product Transfers; Validation / Qualification of new manufacturing suites (Steriles) will also form part of this role. Interaction with multiple functions including R&D, Validation, QC, Manufacturing/Production etc.
Fantastic opportunity to gain experience/exposure to large-scale, high-profile projects on a busy manufacturing site. Fantastic visibility within the organisation and combining QP release and technical project work this will build your profile and acumen to progress quickly within QA. Competitive salary with excellent benefits package and continued professional development. Assitence with relocation is available for the right candidate, as is support with QP training.
QP / Qualified Person (under permanent provisions) status is highly desirable. Equally this opportunity would suit a newly-qualified or trainee QP approaching their Viva. Expert knowledge of GMP / cGMP with significant technical QA experience within a busy manufacturing environment is essential. Whilst ideally you will have worked across a variety of dosage forms; Oral Solid Dose (OSD) manufacturing experience will be especially valuable in this position. Prior experience working on large-scale Technical/Product transfers; setting up a new Sterile manufacturing suite and/or Technical Management experience are all highly desirable.
Key Words: QP | Qualified Person | GMP | cGMP | QA | Quality Assurance | Manufacturing | R&D | IMP | Solid Dose | Sterile | Validation | Qualification | Audit | Internal Audit | External Audit | Technical Transfer | Product Transfer | Pharmaceuticals | East Midlands | Midlands | UK
If you would like to be considered for this opportunity, please click APPLY to send a copy of your CV. For further details and a full job description, please call Joshua Godden on +44 (0) 207 220 6224 or e-mail Joshua.Godden @SkillsAlliance.com. All queries are treated confidentially.
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