£23K/yr to £27K/yr
England, United Kingdom
Temporary, Variable

QA Analyst

Posted by Central Employment Agency (North East) Limited.

Central Employment is delighted to present an opportunity to work in a global pharmaceutical business. The opportunity will be working in the Quality Assurance team creating, monitoring and implementing Quality systems that are required in a pharmaceutical manufacturer. This is an excellent opportunity to join a leading business, understanding the importance of quality, compliance and the systems that underpin and create the foundations for all regulatory requirements. We are looking for candidates with a scientific degree or relevant experience who are looking to build a career in pharmaceuticals and QA.

Key Responsibilities

  • Provide Quality support for regulatory, global QMS and site QMS requirements. Proactively build Quality into site/department processes, systems and strategies to enable a state of permanent inspection readiness.
  • Ability to lead and/or participate in projects liaising with internal and external customers/stakeholders effectively and efficiently. Lead and participate in compliance and continuous improvement activities.
  • Develop proactive relationships with key stakeholders, (internally & externally) and perform all activities in accordance with cGMP requirements.
  • Maintain systems to provide assurance to Site Management of ongoing compliance to applicable Organon and regulatory requirements, including:
  • General Methods
  • Ensure governance and team compliance through company processes, business practices and SOPs to deliver on business goals with the highest level of ethics and integrity.
  • Take accountability for self-development; ensure understanding and application of policies and procedures to enable success for the organisation and to respond to the needs of the business.
  • Provide Support with Audit/inspection requirements to ensure site and department compliance/readiness

Essential Requirements

  • Degree in Chemistry, Pharmacy or other scientific field OR relevant experience

The Person

  • Good written and spoken communication skills and ability to work in and lead cross-functional teams.
  • Ability to form good working relationships with other functional groups.
  • Attention to detail and well-organised approach to working.
  • Ability to be decisive and influence across disciplines and all levels with demonstrated leadership skills to drive change in a compliance culture.
  • Ability to lead and implement multiple projects/tasks simultaneously with competing and/or changing priorities; effective time management.
  • Ability to influence areas not under direct control to achieve objectives and effectively communicate challenging goals
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