Laboratory Supervisor

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.

MAIN RESPONSABILITIES

The role involves supervising laboratory operations, ensuring compliance with quality standards, and driving efficiency through team management, process optimization, and equipment maintenance. It requires expertise in genetics and molecular biology techniques, the ability to work independently, and flexibility to occasionally work evenings and weekends.

• Informs Laboratory Manager of any significant day-to-day operational issues and oversight of the laboratory operation and personnel performing testing.
• Monitoring, coordinating, and supporting all aspects of laboratory operations, including but not limited to inventory, equipment, and training of laboratory personnel. Plan workloads, implement continuous improvement methodologies, and oversee efficiency controls.
• Supervises, orients, and instructs laboratory personnel and assists in performance evaluations.
• Reviews and oversees laboratory Quality Management and Quality Assurance programs.
• Helps troubleshoot equipment issues.

Requirements:

• Degree in Laboratory Science or Medical Laboratory Technology (Ciclos Formativos de Grado Superior).
• Proficiency in standard laboratory techniques, including pipetting, laboratory math, and protocol preparation. Hands-on lab experience is highly preferred.
• Molecular biology expertise, including RNA/DNA extraction (manual and automated), nucleic acid quantification, PCR, RT-PCR, MLPA, and NGS (Thermo Fisher/Illumina platforms).
• Experience in laboratory equipment maintenance, workload organization, and process improvements, with a proven ability to manage change and implement new protocols or systems.
• Familiarity with automated liquid handling equipment is a plus.
• Strong communication skills to explain instrument principles and controls effectively.
• Proficiency in Microsoft Office (Excel, Word, PowerPoint).
• Advanced English skills (written and spoken) are strongly preferred.

Key Knowledge, Skills, and Abilities:

• Strong organizational skills, attention to detail, and a solid work ethic.
• Familiarity with national and international accreditation programs (CLIA, CAP, ISO) and experience with compliance inspections.
• Knowledge of regulatory, quality assurance, quality control, and safety procedures to maintain audit-ready standards.
• Excellent communication, critical thinking, and leadership skills, with experience in process improvement, change management, and team building.
• Ability to multi-task and work efficiently in a fast-paced, deadline-driven environment.
• Proficiency in sterile techniques, manual dexterity for lab equipment use, and comfort working in biohazard environments following safety policies.
• Flexibility to work different shifts, including weekends and holidays, as required.
• Experience in project management and the ability to work independently.

What We Offer:

• Opportunity to work in a leading global organization in healthcare and genetic services.
• Supportive and collaborative work environment.
• Medical insurance.
• Flexible compensation options.
• Free coffee at the workplace.
• Discounts on our platform and gym memberships.
• Job stability in a growing and innovative company.

*The interview will be conducted in English.

We look forward to receiving your application!