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Quality Supervisor

MTrec Recruitment and Training
Job LocationAshington
EducationNot Mentioned
Salary28,000 - 30,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Company DescriptionOur client is a market leader in their sector. Due to growth, they are now looking for a motivated Quality Supervisor who is looking to grasp an outstanding career opportunity, and help a business grow and improve.The Role

  • In this position the Quality Supervisor will support the Quality Manager and have day to day quality responsibility on the manufacturing site.
  • Supervise and train a small team of Quality Technicians ensuring timely inspection of packaging materials, start materials, intermediates and finished products.
  • Release of start, intermediate materials for use in production.
  • Coordinate on site environmental monitoring program, implement best practices, generate and report trend data.
  • Ensure QC activity are aligned with planned production activities.
  • Ensure all activity is in accordance with the principles of pharmaceutical Good Manufacturing Practice and safe working practices.
  • Contributing to the effectivity of the site QMS by reporting and investigating deviation, non-conformance and out of specification results, helping to identify and implement corrective actions to resolve problems and to prevent recurrences.
  • Performing internal audits.
  • Ensuring documentation is completed in accordance with site requirements.
  • Ensuring equipment is calibrated in accordance with identified schedules.
  • Generation of KPI data associated with department and site performance.
  • Ensuring record keeping is in accordance with cGMP guidance.
  • Develop training regime for QC/QA departments and assist in training role out across departments.
  • Carry out COSHH risk assessments.
The Person
  • Previous experience of working in a senior quality role within a manufacturing environment.
  • Experience gained within a pharmaceutical chemical and or cleanroom environment is essential.
  • Previous experience in personnel management and development, ensuring you are able to direct your team to successful completion of all tasks whilst maintaining good morale.
  • Thorough knowledge of ISO quality systems and validation principles for manufacturing processes.
  • Understanding and application of QMS processes, tools and techniques.
  • Sound working knowledge of ISO9001 and GMP requirements.
  • Experience of validation of systems and processes.
  • Strong leadership, communication, and influencing skills in order to work effectively across organizational boundaries and influence decision-makers across multiple sites/regions/levels.
  • With good attention to detail, you approach situations with a meticulous eye on safety, quality and procedures.
  • You will have excellent troubleshooting skills with a focus on finding a solution through to resolution.
  • Good writing and computer skills required for keeping accurate records, writing reports and standard operating procedures.
The Benefits
  • Permanent job.
  • Competitive salary.
  • Opportunity to work for an employer of choice in the region.

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