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Job Title: Professional – Quality Assurance Officer
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Contract: ASAP for 5 months
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Hours:37 hrs p/w
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Location: Marlow (Hybrid)
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Pay rate: 17.67
SRG are working with a global pharmaceutical company who are seeking a QA officer to join their Marlow site.
Role overview
Reporting to a Quality Manager you will provide day-to-day assistance for commercial QA activities associated with effective running of the site QMS supporting batch release. The QA Officer will ensure assigned tasks are performed in a timely manner to meet internal standards and all associated international GMP/GDP requirements.
Primary Duties:
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To assist in maintenance of quality systems including deviations/ exception reporting, change control, supply agreements, document control, quality metrics reporting, training as determined by the QA Manager
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Complete scheduled records and quality system tasks in a timely manner and in compliance with internal standards and EU GMP
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To compile & review Product quality review sets for completeness & compliance to EU GMP, internal requirements and regulatory dossier submissions
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Support in internal audits
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Participate in Quality Risk Management (QRM) assessments
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Project execution and support as required.
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Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Experience and Education Required:
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Experience from a quality-based job role
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2-3 years in a GMP environment
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Basic experience in pharmaceutical manufacturing, distribution, and control measures
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Basic experience in Quality administered systems. Previous use of TrackWise QMS beneficial.
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Ability to apply technical knowledge and understanding to making appropriate and timely risk-based decisions.
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Able to demonstrate good planning and organisational skills
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Attention to detail and accuracy – able to follow verbal and written instruction (SOP’s).
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Quality and process orientation and mindset
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Possession of good verbal and written communication skills
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Sterile injectable manufacture/Manufacture of novel dosage forms is desirable
Carbon60, Lorien & SRG – The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
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Experience from a quality-based job role
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2-3 years in a GMP environment
-
Basic experience in pharmaceutical manufacturing, distribution, and control measures
-
Basic experience in Quality administered systems. Previous use of TrackWise QMS beneficial.
-
Ability to apply technical knowledge and understanding to making appropriate and timely risk-based decisions.
-
Able to demonstrate good planning and organisational skills
-
Attention to detail and accuracy – able to follow verbal and written instruction (SOP’s).
-
Quality and process orientation and mindset
-
Possession of good verbal and written communication skills
-
Sterile injectable manufacture/Manufacture of novel dosage forms is desirable
Contact Detail:
SRG Recruiting Team