Laboratory Analyst with Disability Certificate

• Disability Certificate of 33% or higher is essential.

-Higher Vocational Training Degree in Chemistry and/or Clinical

-experience or specific training in Quality Control and Processes.

-Knowledge of GMPs and medical device manufacturing standards

-Ease in dealing with people and teamwork.

-Basic level of English.

-Skill in computer use.

• Must have own vehicle. The factory is difficult to access without a personal vehicle.

• Contract to be determined. With the possibility of permanent employment.

-Gross annual salary: From €27,000 to €32,000, experience will be valued.

Monday to Friday, in 3 shifts (flexibility):

Morning: 06:00h to 14:00h.

Afternoon: 14:00h to 22:00h.

Night: 22:00h to 06:00h.

• Excellent working environment
• Immediate start

Do you have experience as a laboratory analyst and do you have a disability certificate? At Fundación Randstad, we have an opportunity for you.

Execute the processes described in the Management System that ensure starting materials (raw materials and packaging materials) and manufactured products meet the specified requirements; where applicable, initiate the Non-Conforming product Control process. Continuous improvement focused on quality requirements and supplier efficiency. Participation in Innovation projects.

-Inspection and testing A) Sampling and Inspection: Sampling. qualitative inspection of raw materials. CoA data processing.

B) Quantitative Inspection, Analysis and Testing: Quantitative inspection through testing of Raw Materials and products in the manufacturing process in accordance with QS provisions, requiring the use of complex instrumental analysis.

C) Laboratory Management: Control of materials including PPE, reagents. Control of documentation and Records. Laboratory safety management.

2 Process Control

D) Qualitative Inspection (In Process Control-IPC): Direct qualitative inspection in production (IPC), set quotas, and ensure that production processes are carried out according to approved manufacturing instructions and in the required environment. Approve IPC protocols. Make usage decisions.

E) Non-Conforming Product Management: Initiate and Evaluate non-conforming products. Assist Production in the identification, separation, and review of non-conforming products.

3 Analytical Development

F) Analytical Development: Validation and transfer of testing methods, Training and Qualification of analysts. Instrumentation management - Maintenance and Calibration.

4 Process and Supplier Improvement

G) Process Validation: Based on continuous process improvement, ensure that processes generate products with the required quality, managing the necessary actions to correct the causes of non-conformities or the necessary actions to control their occurrence.

H) Continuous Improvement of supplier efficiency: Ensure that the capacity of supplier processes is adequate to supply products with the required quality.