QC TECHNICIAN MICROBIOLOGY

MCR International; Asturias; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A major healthcare company in Asturias is seeking a detail-oriented QC Technician - Microbiology. In this role, you will oversee laboratory operations ensuring compliance with GMP standards and facilitate continuous improvement initiatives. The ideal candidate will have a Degree in Biology with a specialization in Microbiology and at least 1 year of experience in Quality Control within the pharmaceutical sector. Competitive compensation and opportunities for professional growth offered.

Servicios

Dynamic and collaborative work environment

Opportunities for professional growth

Competitive compensation and benefits package

Formación

• Minimum 1 year of experience in Quality Control within the pharmaceutical industry specialized in Microbiology.

Responsabilidades

• Ensure compliance with company procedures on Safety, Environment, and Quality.
• Supervise and guide analysts in performing laboratory tests and activities.
• Review and approve analytical documentation including test results.
• Collaborate in drafting SOPs and specifications.
• Manage SAP entries for results and batch management.
• Oversee calibration and qualification of laboratory instruments.
• Drive continuous improvement projects and promote process optimization.

Conocimientos

Communication skills

Problem-solving skills

Educación

Degree in Biology or related field

Microbiology specialization

Descripción del empleo

AH-2511-401
QC TECHNICIAN MICROBIOLOGY
ASTURIAS

About the Role

We are looking for a highly skilled and detail-oriented QC Technician - Microbiology to join an important healthcare company. In this role, you will lead and oversee critical laboratory operations, ensuring compliance with GMP standards and regulatory requirements. You will play a key part in maintaining the integrity of the quality systems, driving process automation, and supporting continuous improvement initiatives.

Key Responsibilities

• Ensure compliance with company procedures on Safety, Environment, and Quality.
• Supervise and guide analysts in performing laboratory tests and activities.
• Review and approve analytical documentation, including test results, certificates of analysis, stability studies, and supplier qualifications.
• Collaborate in drafting SOPs, specifications, analytical methods, and stability protocols.
• Manage SAP entries for results, batch management, and material creation.
• Guarantee proper packaging and custody of QC samples (stability, cleaning, reference standards).
• Oversee calibration and qualification of laboratory instruments and maintain related documentation.
• Lead technical services activities: equipment calibration, qualification, and lifecycle management.
• Maintain updated procedures for computerized systems validation and ensure data integrity.
• Manage supplier qualification for services and equipment.
• Evaluate and review data from external laboratories.
• Drive continuous improvement projects and promote process optimization and automation.
• Support production and analytical development activities (method validations, transfers, investigations).
• Collaborate in aseptic process simulation design and execution.
• Provide technical support during audits and inspections by health authorities.
• Assist in preparing responses to technical inquiries from clients and regulatory bodies.
• Contribute to internal training and analyst qualification programs.

Regulatory & Quality Compliance

• Update laboratory procedures to meet GMP and pharmacopeia requirements.
• Review validation protocols and reports to ensure regulatory compliance.
• Participate in risk assessments, deviation investigations, and CAPA implementation.

What They Offer

• A dynamic and collaborative work environment.
• Opportunities for professional growth and involvement in innovation and automation projects.
• Exposure to international standards and interaction with health authorities and global suppliers.
• Competitive compensation and benefits package.

Qualifications

• Degree in Biology or related field.
• Valuable Microbiology specialization.
• Minimum 1 year of experience in Quality Control within the pharmaceutical industry working specialized in Microbiology.
• Excellent communication, and problem-solving skills.