Shift QA Officer, Pharmaceutical - Skipton

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Irfa******

  • United Kingdom 
  • Last Update: 19.10.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
3 Month +
Place
Skipton, GB
Country
United Kingdom

Description


Job Title Shift QA Officer Location Skipton Salary Range 20 26k 14 uplift Hours 6am2 30PM or 2 30Pm10PM Monday to Friday This would suit a candidate with an Operational Quality background ideally 2 years in GMP Manufacturing Job Purpose and Key Accountabilities of the Shift QA Officer The Shift QA Officer works closely with operational teams quality control team engineering team and other support function to ensure compliance to relevant SOPs and GMP standards and delivery of site quality metrics li Perform in processchecks to ensure Quality based systems and procedures are followed within the operations functions Makes decisions and recommendations on actions needed to resolve technical and GMP compliance issues li li Provide guidance on operational changes and improvements li li Support internal and external quality technical audits li li Training of new team members Provide technical training on current and emerging regulatory requirements li li To be located in operations and ensure that GMP Quality batch specific and where applicable client requirements are being adhered to at all times within the Operations area li li Display GMP attitude at all times li li Participate in CI activities and projects through challenging current working practices with a view of improving efficiencies and Quality standards li li Prioritise workload and ensure key quality issues and business priorities are addressed and escalated appropriately and resolved in a timely manner li li Assist in quality investigations and participate in incident meetings li li Verify cGMP data entries into site computer systems li li Participate in required site meetings as representatives of Quality when required li li Apply problem solving capabilities to determine root causes of issues and identify effective CAPA to increase right first time and improve efficiencies and reduce operating costs li li Review batch documentation for adherence to cGMP compliance li Qualifications em Essential em li GMP knowledge li li GCSEs A levels or equivalent li em Desireable em li Educated to degree level or equivalent in Chemistry Pharmaceutical Science Life Science Engineering or other similar disciplines li Knowledge and Experience for the Shift QA Officer em Essential em li Must have previous experience of working in a cGMP manufacturing environment li li Experience and ability to drive issues through to satisfactory conclusion li li Experience of assimilating contents of written documents quickly and accurately li li Ability to work in cross functional teams li em Desireable em li Ideally previous experience of working in a Quality environment li li Knowledge of document systems and indexing are desirable li li General appreciation of factory operating systems is desirable li Please contact Mustafa Ahmad at Science Solutions Required skills li class lozenge skillname Compliance li li class lozenge skillname Quality Assurance li li class lozenge skillname Veterinary li li class lozenge skillname Pharmaceuticals li

Seniority Level

Entry level

Industry

    • Staffing

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