Company

Biotech

BiologicalSafetySpecialist

€38–55k ~AI est. Spain FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Biological Safety Specialist. Skills: Biological safety, Biocompatibility, Regulatory documentation. Develop biological safety documentation. Review biological safety documentation”

What You'll Achieve.

Ensure products meet standards; Influence product approval; Influence market readiness

Industry & Context.

Biotech
Problems you'll solve

Analytical thinking; Critical thinking

What They're Looking For.

Must Have

Bachelor's degree with at least 5 years of relevant experience, Master's/Doctorate degree with at least 2 years of relevant experience, Knowledge of medical device regulations, Knowledge of international standards related to biological safety, Knowledge of biocompatibility, Experience assessing compliance of biocompatibility studies, Experience assessing material characterization against regulatory requirements, Proven ability to write complex technical documentation, Proven ability to review complex technical documentation, Proven ability to manage complex technical documentation, Proven ability to write regulatory documentation, Proven ability to review regulatory documentation, Proven ability to manage regulatory documentation, Analytical and critical thinking skills, Proficiency in Microsoft Word, Proficiency in other standard documentation tools, Fluency in proficiency in the local language

Nice to Have

Master's degree with at least 2 years of relevant experience, Doctorate degree with at least 2 years of relevant experience

What You'll Do.

Develop biological safety documentation

Review biological safety documentation

Maintain biological safety documentation

Develop biological safety reports

Review biological safety reports

Maintain biological safety reports

Assess biocompatibility data

Audit biocompatibility data

Assess material characterization data

Audit material characterization data

Interpret scientific information

Interpret technical information

Support risk assessments

Support regulatory submissions

Collaborate with cross-functional teams

Integrate biological safety considerations

Review technical documents

Contribute to technical documents

Review regulatory documents

Contribute to regulatory documents

Support continuous improvement

Improve biological safety processes

Improve biological safety methodologies

Improve compliance frameworks

How You'll Work.

Team & Collaboration

Cross-functional teams; Multidisciplinary teams; External stakeholders

Full Job Description

## Description This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Biological Safety Specialist based in Spain. This role sits at the intersection of science, regulation, and medical device innovation, ensuring that products meet the highest standards of biological safety throughout their development lifecycle. You will contribute directly to the safety and compliance of medical technologies that impact patient health globally. Working within a highly specialized and regulated environment, you will evaluate scientific data, assess biocompatibility, and support the creation of critical regulatory documentation. The position involves close collaboration with multidisciplinary teams and external stakeholders to ensure alignment with international standards. You will play a key role in shaping safety assessments that influence product approval and market readiness. This is a detail-driven and impact-focused role suited for professionals passionate about science, compliance, and healthcare innovation. ## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant

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