Senior Quality Controller – Praca – Poznań, Sady

Lina Medical; Poznań; Hybrid; PLN 60,000 - 95,000; Full time

Benefits offered by this job

Private medical care

Sports card

Flexible working time

Home Office

Co-financing for English language

Job summary

Lina Medical in Poznań is seeking a Quality Control specialist to oversee incoming inspections, document control, and final product testing. You will collaborate with R&D and production, select measuring equipment, and support audits to ensure compliance with ISO 13485.

The role requires 2 years in QC, familiarity with medical device standards, and good English communication. Training and career growth opportunities are offered in an international setting.

Qualifications

• Minimum 2 years of experience in Quality Control.
• Experience in Medical Devices or Pharmaceutical industry is an advantage.
• Conversational English – verbal and written.
• Knowledge of technical drawing.
• Auditing experience is an advantage.

Responsibilities

• Collaborate with R&D and production teams to supervise the introduction of new components.
• Oversee selection of measuring equipment for processes.
• Create and maintain quality documentation and assist in approvals of technical docs.
• Supervise incoming materials, testing, and documentation.
• Oversee final product inspections and reporting of performance.
• Participate in internal and external audits.
• Lead quality investigations and corrective actions.

Skills

Quality control

Quality assurance

Auditing

English communication

Technical drawing

ISO 13485

Medical devices

Education

Relevant education

Tools

Keyence

Job description

Essential job functions :

• Strick cooperation with R&D department in Denmark and all linked departments in Poland;
• Supervision over the introduction of new components into production;
• Creation of quality documentation and support in the creation and approval of technical documentation;
• Supervision over the selection of measuring equipment for process;
• Incoming processes supervision and its documenting;
• Ad hoc problem solving in area of Incoming Inspection;
• Incoming inspection responsible including performance and documentation;
• Final Control of product including performance and documentation;
• Participation in non-conformance process;
• Measuring equipment- operation and design (Keyence);
• Collection of raw materials? batch certificates (CoC; Quality Certificates; etc);
• Creating documents according existing procedures;
• Coordinator of Nice Label system;
• Participation in internal and external audits;
• Quality investigations and training.

Education and Experience:

• 2 years of experience in Quality Control
• Work experience within Medical Devices or Pharmaceutical industry is an advantage;
• Conversational English ? verbal and written;
• Relevant education and/or experience;
• Experience in auditing is an advantage;
• Fast learning and open minded;
• Knowledge of technical drawing;
• Efficient, accurate, work according to plan;
• Flexible, pro-active & hard working;
• Familiar with ISO 13485;
• Fast learning and open minded;
• Knowledge of technical drawing;
• Efficient, accurate, work according to plan;
• Flexible, pro-active & hard working;
• High profile commitment to Quality;
• Positive & problem solving attitude;
• Team Player.

We offer:

• Full-time job contract;
• Opportunity to work in an international environment;
• A number of benefits (private medical care, sports card, flexible working time, Home Office, co-financing of holidays, co-financing for English language classes, fruit and snacks);
• Great atmosphere in the office and interesting challenges;
• Opportunity to grow with the organization and build a successful career path;
• Internal and external training.