Onsite Specialist II, Scientific Support

Avantor

Toledo

On-site

EUR 42,000 - 54,000

Full time

4 days ago
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Job summary

Avantor is currently seeking an Onsite Specialist II, Scientific Support to assist in High-Throughput Purification within the ACHTP platform. The role supports drug discovery programs, delivering purified compounds and maintaining rigorous data integrity.

Fluency in Spanish and the ability to collaborate across disciplines are valued in this onsite, customer-facing position. You will perform purification using HPLC/SFC, manage samples and data, and contribute to continuous improvement of

Qualifications

  • Education preferably BSc or MSc in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Or equivalent based on experience.
  • Experience and Technical Skills Experience with chromatographic techniques, particularly reversed-phase HPLC and/or SFC, is preferred.
  • Previous experience in an analytical laboratory, pharmaceutical R&D, or a related scientific environment is advantageous.
  • Familiarity with laboratory data systems, scientific documentation, and good laboratory practices.
  • Ability to learn new technologies, procedures, and technical skills quickly.
  • Strong attention to detail and commitment to accurate, high-quality work.

Responsibilities

  • Perform routine and complex compound purification using reversed-phase HPLC and SFC technologies in accordance with established procedures and guidelines.
  • Conduct post-purification processing and ensure compounds are prepared for delivery to project teams.
  • Ensure accurate sample handling, tracking, labelling, and documentation throughout the purification workflow.
  • Maintain high productivity while meeting quality, safety, compliance, and data integrity requirements.
  • Deliver purified compounds within agreed timelines to support medicinal chemistry and drug discovery projects.
  • Use laboratory data systems and related software to record, review, and manage experimental information.
  • Troubleshoot routine technical issues and escalation complex problems appropriately.
  • Work collaboratively within a multidisciplinary ACHTP environment.
  • Contribute to continuous improvement of laboratory workflows and operational efficiency.

Skills

Chromatography
Laboratory data systems
Analytical chemistry

Education

BSc or MSc in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

HPLC
SFC

Job description

The Opportunity

Carries out a range of complex scientific support tasks at customer facilities, requiring significant interpretation of technical/scientific protocols to support research objectives effectively. Solves intricate research support and technical challenges independently, drawing on a deep understanding of laboratory techniques, experimental design, and past experiences to inform judgments and decisions. Supports nucleic acid workflows, performs DNA/RNA extraction and preparation for sequencing, and/or maintains and expands cell and tissue cultures, supporting R&D and production workflows. Collects, documents, and organizes data and observations, ensuring clarity and accessibility for review and analysis by research teams. Collaborates extensively with internal scientific support teams and customer contacts, facilitating communication and understanding across disciplines to meet customer's needs.

Scientific services support Location: J&J, Toledo, Spain Workplace: Onsite at the customer through VWR Platform: Analytical Chemistry & High-Throughput Purification (ACHTP) Position Summary The Onsite Specialist II, Scientific Support will support the High-Throughput Purification (HTP) function within the Analytical Chemistry & High-Throughput Purification (ACHTP) platform, contributing to the efficient delivery of purification services that support drug discovery programs.

Key Responsibilities
  • Perform routine and complex compound purification using reversed-phase HPLC and SFC technologies in accordance with established procedures and guidelines.
  • Conduct post-purification processing and ensure compounds are prepared for delivery to project teams.
  • Ensure accurate sample handling, tracking, labelling, and documentation throughout the purification workflow.
  • Maintain high productivity while meeting quality, safety, compliance, and data integrity requirements.
  • Deliver purified compounds within agreed timelines to support medicinal chemistry and drug discovery projects.
  • Use laboratory data systems and related software to record, review, and manage experimental information.
  • Troubleshoot routine technical issues and escalation complex problems appropriately.
  • Work collaboratively within a multidisciplinary ACHTP environment.
  • Contribute to continuous improvement of laboratory workflows and operational efficiency.
Qualifications
  • Education Preferably BSc or MSc in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Or equivalent based on experience.
  • Experience and Technical Skills Experience with chromatographic techniques, particularly reversed-phase HPLC and/or SFC, is preferred.
  • Previous experience in an analytical laboratory, pharmaceutical R&D, or a related scientific environment is advantageous.
  • Familiarity with laboratory data systems, scientific documentation, and good laboratory practices.
  • Ability to learn new technologies, procedures, and technical skills quickly.
  • Strong attention to detail and commitment to accurate, high-quality work.
Personal Attributes
  • High level of ownership, accountability, and reliability.
  • Effective communication and collaboration skills.
  • Ability to work productively in a fast-paced, multidisciplinary environment.
  • Strong organisational and time-management skills.
  • Commitment to safety, compliance, data integrity, and operational excellence.
Languages
  • Fluent Spanish is highly desirable.
  • Basic working knowledge of English is preferred.
Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world.

EEO Statement

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information.

Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Privacy Policy

We will use the personal information that you have submitted to us in order to consider your application for the relevant role. Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests.

3rd Party Non-Solicitation Policy

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

Avantor, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers. Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.

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