Job details

Quality Control Manager

Company details

Profile Group is a premium Selection and Recruitment company that has been helping candidates in their job search for 30 years. Working with a wide variety of companies, we provide candidates with a high quality service that helps both in the application process and improving the various skills required to succeed in interviews.
Our client, Physiol, a member of the BVI group specialized in ophthalmic surgery, is involved in the research, development and manufacture of intraocular implants for cataract surgery.

Function

As a QC Manager, you have the following responsibilities:


Post Market Surveillance

  • You work closely with RA/QA, R&D, Industrialisation, Operations, Clinical and other functional areas to evaluate actual of potential product failures and update risk management files as needed
  • You support QA in the Complaint management process and you are responsible for managing a team in charge of investigating, determining root cause and ultimate resolution of product failures
  • You contribute to product safety, product quality and customer satisfaction related decisions
  • You participate and support internal and external supplier audits and inspections
  • You monitor and advise on how the product quality is performing and publishes data and reports regarding the effectiveness of the quality management system


Product Acceptance & Investigations

  • You plan and conduct the analysis, inspection, design, tests and/or integration of test methods to assure the quality of assigned products or components
  • You develop test methods and participate in the assessment of returned products, incoming, in-process and final test/inspection.
  • You apply statistical process control (SPC) methods for analyzing data to evaluate the current process and process changes
  • You coordinate the documentation review, inspection workflow, training, problem solving and calibration for test equipment
  • You advise on changes and their implementation and provides training, tools and techniques to enable others to achieve quality
  • You utilize statistical analysis techniques to determine product acceptance and AQL sampling plans, evaluate process capabilities and develop statistically sound tolerance limits
  • You participate in the non-conformance reporting system. You identify non-conformance trends and develop and administer technical investigation and corrective action programs.

Product Development & Operations

  • You collaborate with R&D in the development and implementation of product test plans including Verification and Validation of products and processes
  • You serve as liaison to design, procurement and manufacturing engineering
  • You participate and / or lead validation programs of processes and product
  • You perform standard quality engineering reviews of design documentation for compliance with stated requirements, including supplier quality and company quality records
  • You work with Manufacturing Engineering to address supplier quality issues

Tags: quality, quality assurance manager, quality control, QHSE manager, quality engineer, quality supervisor, quality control manager, QC, quality & compliance engineer, medical devices, assurance qualité, controle qualité, ingénieur qualité, biotech, pharma

Profile

Required education and experience:

  • You have a master's degree in science or another technical field
  • You have a minimum of 8 years’ experience with a first experience as a team leader in the medical device, Pharma industry or any other compliant environment.
  • You have knowledge in Medical device Quality system, including 21 CFR Part 820 (QSR) & ISO 13485
  • You demonstrate skills in statistical analysis
  • You have experience in internal and external audit
  • You have experience with CAPA, complaint investigation, field action processes and risk management
  • You have strong computer skills

General and behavioural skills and competencies:

  • You have team leadership spirit
  • You are recognized as a technical leader in the company
  • You are able to lead a Continuous improvement Team, CAPA team, or working with a customer or supplier to resolve product quality issues
  • You are assertive and unifying, you have a sense of dialogue and compromise
  • You are self-sufficient

Language

FR/EN

Offer

You join a dynamic and state-of-the-art environment in a company that encourages its teams to take initiatives and bring ideas that contribute to the success of the company. Physiol offers you a position of responsibility, with a competitive salary package.

  • Placed on:Wed 13 May 2020
  • Location: Liège

Profile Group

Quai Mativa 62
4020 Liège

E-mail

Interested?

For more information:
Call ANAELLE HENRARD
at the number: 0470 40 77 30
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