Quality Assurance Officer

• Job Title: Professional – Quality Assurance Officer

• Contract: ASAP for 5 months

• Hours:37 hrs p/w

• Location: Marlow (Hybrid)

• 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:

• 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

• Complete scheduled records and quality system tasks in a timely manner and in compliance with internal standards and EU GMP

• To compile & review Product quality review sets for completeness & compliance to EU GMP, internal requirements and regulatory dossier submissions

• Support in internal audits

• Participate in Quality Risk Management (QRM) assessments

• Project execution and support as required.

• 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:

• Experience from a quality-based job role

• 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

Carbon60, Lorien & SRG – The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

• Experience from a quality-based job role

• 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