Contract Manufacturing Quality Manager
Kingston upon Hull, East Yorkshire, GB
1d ago


Contract Manufacturing Quality Manager

Kingston upon Hull, East Yorkshire

Competitive Salary & excellent benefits package

This role provides an exciting opportunity to manage the Quality team in our contract manufacturing area, producing solid dose and sterile injectable dosage forms.

This role will provide strong leadership and external stakeholder management whilst driving a Quality culture of continuous improvement.

The role will have direct management of the quality assurance team for the areas whilst also being the primary quality contact for our external customer.

In this role you'll be :

  • Working as part of the site leadership management team, alongside all factory support functions, providing quality support and QA expertise
  • Managing the quality assurance team for the contract manufacturing area
  • Acting as the primary Quality contact for customer relations
  • Ensuring EU GMP quality requirements are met for all product manufacture with the EU
  • Ensuring factory activities are fully compliant with regulatory and Reckitt guidelines to minimise risk to consumers, company and brand name
  • Ensuring hat any risks are assessed, identified, and documented, prior to batch release with minimum risk of non-compliance to EU GMP and the Market Authorisation
  • Making sure targets for quality improvement plans are met in alignment with customer expectations
  • Facilitate the identification, communication, and the ongoing removal of identified quality and compliance risks
  • Providing quality oversight of validation activity relating to facilities, introduction of new equipment, changes to current equipment, NPD EPD and product transfers
  • You’ll succeed because you

  • Are a Certified QP named on MIA license (minimum 2 years QP batch release)
  • Possess a broad understanding of manufacturing operations and quality management systems
  • Have pharmaceutical cGMP / manufacturing experience, including a good understanding of RB pharmaceutical manufacturing and QC testing operations
  • Hold a range of dosage form experience : Solid dose, Liquid dose, Sterile all preferable
  • Have experience of validation, training, auditing and risk management
  • Demonstrate strong stake holder management and relationship building skills
  • Have effective communication, presentation and influencing skills
  • Are able to work with and influence cross functional teams and external stakeholders
  • You'll love it because...

  • You will be providing the quality framework and infrastructure to support contract manufacturing operational activities, ensuring continued compliance to EU GMP, to facilitate global supply of licensed products
  • You will be managing operational QA teams, ensuring compliance to cGMP requirements in all areas of operations
  • You will be joining a global consumer goods manufacturer with excellent career progression opportunities within
  • Equality

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