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Quality Manager

Quality Manager

Job Title: Quality Manager
Contract Type: Permanent
Location: Blackwood, Caerphilly
Industry: Pharmaceutical
Reference: HQ00004430_1604575501
Contact Name: Angharad Isaac
Contact Email:
Job Published: 05 November 2020
Job Description

Quality Assurance Manager
Salary: £50,000 - £55,000 per annum plus benefits
Permanent
Blackwood

Do you want to be part of a business that makes a real-world impact? Helping to play a role in finding cures for cancer and protecting the environment? You will be fully supported in achieving your goals and will reap the rewards.


Reporting directly to the Quality Assurance Director you will provide leadership of the Quality function to the Blackwood site. This key leadership position is accountable for improving product and process quality. Leading the development, sustaining and improvement of the quality management system and managing customer expectations. In addition, you would be responsible to structure and develop the QA team in support of business growth while creating a culture where everyone owns quality.

Key duties and responsibilities
Sets the overall quality strategy for the manufacturing site that supports growth and compliance readiness.
Actively participates in quality improvement projects to move the organization to rely less on inspections and more on quality assurance.
Carries out leadership responsibilities in accordance with the organisation's policies and applicable laws. Responsibilities include interviewing, hiring, developing, and training employees; planning, assigning, and directing work; appraising performance; rewarding, discipline of employees; addressing complaints and resolving problems.
Provides leadership and coaching to Operations Quality, Quality Systems, and Technical Quality/Quality Engineering teams (5-8 direct reports; total QA team: 10-15 employees).
Leads, maintains and creates efficiencies in the Quality Management System to fulfill international quality system requirements (e.g. 21 CFR 820, ISO 9001, ISO 13485, and IVDR).
Assures management reviews of the Quality System are held and properly documented to reflect the status of the Quality System effectivenes, resulting in corrective actions and improvement plans/actions.
Works closely with all staff to ensure that all aspects of the QMS is understood, implemented and maintained.
Creates cross functional collaboration and influences all business functions to apply appropriate quality tools including Lean, Six Sigma, TQM principles, business process improvement methods and statistical methods (e.g. design of experiments, statistical process control).
Maintains alliance with Divisional, Group, and corporate Quality and Regulatory Affairs to ensure participation in and understanding of associated initiatives.
Effectively manages Corrective and Preventive Action System. Works with various departments to identify actions required to assure corrective and preventative actions are properly documented and follows up to initiate and monitor timely completion of actions.
Oversees the Internal Audit programme assuring compliance with regulatory standards. Coordinate and participate in any external or customer audits.
Sets site wide QA/QC priorities and key objectives to reduce the cost of poor quality and improve the compliance to regulations and the site Quality System.
Manages Key Quality Business Metrics and Department Metrics.
Acts as the site Quality Representative with third party agencies, regulatory agencies and any government agency.
Other duties may be assigned, as required.

Minimum Requirements/Qualifications
5+years Quality Manager experience in IVDD, ISO 9001 and ISO 13485 certified medical-device manufacturing company.
Extensive quality management experience in a high-volume environment.
Experience with problem-solving techniques such as PPI, 8D, DMAIC, PPS
Experience with FMEA and other risk management tools
Strong, proven leadership, communication, and personnel management skills that inspire and motivate a team. Must have had experience with formal goal and objectives setting.
Effective written and oral communication skills in English.
5%-10% travel requirement.

Preferred
ASQ Quality Engineer or Certified Quality Manager; ASQ lead auditor training 3rd-party training record on ISO 13485 and risk management (ISO 14971)
Experience with Lean or Six Sigma improvement systems
Experience in high volume plastics/molding industry.

Vibe Recruit is acting as an Employment Agency in relation to this vacancy.

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