QC Supervisor

UQUIFA; Sant Celoni; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A pharmaceutical company in Sant Celoni, Spain, is seeking a QC Supervisor to manage daily laboratory activities, ensure product quality, and support a team of analysts. Candidates should have a degree in Analytical Chemistry and experience in GMP environments. The position offers an indefinite-term contract and a salary package including bonuses.

Servicios

Indefinite-term contract

Salary package includes bonus

Good training plan

Shift work (M/T)

Formación

• Consolidated experience in analytical techniques, preferably in GMP environments.
• Experience in team management.
• Fluent in English and Spanish (spoken and written).

Responsabilidades

• Coordinate and supervise activities in the QC Laboratory.
• Release and/or reject raw materials and intermediates.
• Manage and issue certificates of analysis.
• Provide technical support to analysts.
• Investigate unexpected results.

Conocimientos

Analytical techniques

Planning skills

Communication skills

Team management

Fluent in English

Fluent in Spanish

Educación

Degree in Analytical Chemistry

Descripción del empleo

About The Role

As Qc Supervisor under supervision of the QC Laboratory Analysis Manager , will be responsible for the daily management of the QC Laboratory performing the following functions:

• Coordination and supervision of the activities carried out in the QC Laboratory.
• Release and/or rejection of raw materials and intermediates in the system.
• Management, issuance and signature of certificates of analysis sent to customers.
• Technical support to the analysts during the analysis and in all the activities related to the laboratory, as well as their continuous training.
• Editing of the weekly and daily planning and distribution of tasks of the analysts to achieve the fulfillment of the planning.
• Investigation of unexpected results (out of specification and/or out of trend) obtained in the laboratory.
• Issuance of investigation reports of unexpected results for CMO products.
• Notification and investigation of deviations generated.
• Collaboration in the elaboration and/or control of the KPI's of the department.

Experience And Attributes We Value

• Degree in Analytical Chemistry.
• Consolidated experience in analytical techniques, preferably in GMP environments.
• Planning and communication skills.
• Experience in team management.
• Fluent English and spanish (spoken and written).

What's on Offer

• Indefinite-term contract
• Salary package of fixed salary plus bonus
• Good training plan
• Shift work ( M/T)