QC Supervisor

Chemo; León; On-site; EUR 28,000 - 42,000; Full time

Benefits offered by this job

Subsidised canteen

Employee benefits

Career progression

Ongoing training

Innovative working environment

Job summary

INSUD PHARMA, operating across the pharmaceutical value chain, is seeking a QC professional in León to oversee finished, intermediate and raw materials analysis. You will ensure compliance with GMP/GLP, coordinate sampling, and support internal and external audits.

Responsibilities include calibrating QC equipment, reviewing reports, and maintaining SAP records while enabling efficient release processes and continuous improvement in a global setting.

Qualifications

• University degree in Chemistry or a related field.
• Knowledge of GMP and GLP regulations.
• High level of Spanish and English.
• Willingness to travel occasionally.

Responsibilities

• Organize and control analysis of finished, intermediate or raw materials for their release following approved analytical methods.
• Schedule and control microbiological sampling in manufacturing areas (water, air, surfaces).
• Coordinate technicians to manage sampling of materials and products.
• Ensure QC equipment is calibrated/verified before use.
• Review QC analytical reports and input results into SAP.

Skills

Analytical skills

Accuracy

Reliability

Teamwork

Education

University degree in Chemistry or similar

Job description

Experience: Minimum 3 years’ experience in the functions mentioned above.

INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health.

The activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo) and Branded (Exeltis), with over 9,000 professionals in more than 50 countries, 20 state‑of‑the‑art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development.

Global Responsibility

Follow established procedures and guidelines to check, test, and inspect raw materials, goods in process, and finished goods.

Coordinate, evaluate and monitor technical, human resources, the results section, the results, and to inform internal and external auditors; according to the GMP regulations, methods and procedure of the plant, in order to achieve the completion of all work related to the products produced by the plant, provide technical support to internal external companies (clients) and (production) and get a good score evaluations audits. All this taking into account the safety regulations indicated by the company and the use of personal protective equipment provided depending on the risks of each operation.

Specific Responsibilities

• Organize and control the analysis of finished, intermediate or raw materials for their release following approved analytical methods, SOPs or quality guidelines.
• Schedule and control water, air and surfaces microbiological sampling in manufacturing areas.
• Coordination of the technician in order to manage the sampling of raw material, intermediate and finished products.
• Assure Quality Control equipment’s are calibrated/verified before use.
• Review Quality Control analytical reports.
• Add analytical results in inspection lot of SAP system after analysis were completed.
• Compare the physical characteristics of components, materials, equipment, and products to technical specifications to identify defects.
• Provide technical support to internal and external customers.
• Supervise the test performed by analysts and technicians, providing technical support
• Evaluate the work of Quality Control staff to present the Quality Control Responsible their skills and attitudes.
• Prepare CAPAs
• Management of the change controls related to analytical laboratory
• Achieve the company targets
• Organize the workload in order to meet established objectives for product analysis
• Optimize the lead times of the release products

Innovation, customer orientation, communication, teamwork, adaptability/flexibility, productivity, Self-development, sense of urgency, initiative.

Accountabilities

KPI related to the job.

Requirements and personal skills

• Education: University degree in Chemistry or similar.
• Languages: High level of Spanish and English is necessary.
• Experience (years/area): Minimum 3 years’ experience in the functions mentioned above.
• Specific Knowledge: Knowledge of GMP, GLP regulations and Leon Farma SOP’s.
• Travels: Open to travel occasionally.
• Personal skills: good analytical skills, accuracy and reliable, team worker.

Career progression and development within a growing international group

Ongoing training and an innovative working environment

Subsidised canteen and other employee benefits

What will the recruitment process be like?

Initial contact by phone or email with our Talent Acquisition team. 1 or 2 face‑to‑face interviews at our premises in León. Regular updates on the progress of the process.

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