Analyst, Pharmaceutical Development

Jobtailor; Sintra; Presencial; EUR 25 000 - 42 000; Tempo integral

Resumo da oferta

Jobtailor in Portugal seeks an analytical lab professional to join the quality team. You will perform method validation, verification, transfers and stability sampling, generating reports and CoAs to support regulatory compliance.

You will manage critical documents, CAPA, and assist in audits while acting as primary site contact for new product introductions across sites, ensuring SOP adherence and GMP compliance worldwide.

Qualificações

• Bachelor’s degree in chemical engineering, chemistry or similar.
• Demonstrated knowledge of working in an analytical lab environment, of the cGMPs, and should have the ability to follow SOPs and policies.
• Demonstrated ability and skill to perform required analytical techniques and to operate and troubleshoot the associated equipment and software.
• Capability of working with others and as part of a team is essential.
• Good problem-solving techniques is needed to make necessary adjustments and to prioritize tasks.

Responsabilidades

• Stays updated with regulatory and quality standards, evolutions in GXP compliance and best practices where needed everywhere in the world.
• Performs required Method validation, verification, transfer and stability samples analytical work and fills out relevant documentation, including generating reports and filling CoAs.
• Performs request, label and management of assigned products process validation batches and stability samples for the new geographical and presentations filings.
• Supports the management of critical documents and CAPA in addition to the preparation of quality management and audit reviews.
• Acts as primary contact for the related sites to support the introduction of assigned products for the identified purpose.
• Ability to remain update in all analytical techniques required.

Conhecimentos

Analytical skills

Team player

Problem solving

Laboratory experience

cGMP knowledge

Formação académica

Bachelor’s degree in Chemical Engineering or Chemistry

Descrição da oferta de emprego

Responsibilities

• Stays updated with regulatory and quality standards, evolutions in GXP compliance and best practices where needed everywhere in the world
• Performs required Method validation, verification, transfer and stability samples analytical work and fills out relevant documentation, including generating reports and filling CoAs.
• Performs request, label and management of assigned products process validation batches and stability samples for the new geographical and presentations filings.
• Supports the management of critical documents and CAPA in addition to the preparation of quality management and audit reviews.
• Acts as primary contact for the related sites to support the introduction of assigned products for the identified purpose.
• Ability to remain update in all analytical techniques required.

Requirements

• Bachelor’s degree in chemical engineering, chemistry or similar;
• Demonstrated knowledge of working in an analytical lab environment, of the cGMPs, and should have the ability to follow SOPs and policies;
• Demonstrated ability and skill to perform required analytical techniques and to operate and troubleshoot the associated equipment and software;
• Capability of working with others and as part of a team is essential;
• Good problem-solving techniques is needed to make necessary adjustments and to prioritize tasks.