Quality Control Technician Support Services

3PBIOVIAN; Noáin; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A biopharmaceutical company in Navarra is seeking a Quality Control professional to join their team. The role involves generating documentation, reviewing compliance of analyses, and ensuring the quality of materials. Candidates should possess a degree in a related field, advanced English skills, and relevant experience in molecular biology and regulatory guidelines. The company offers a flexible compensation plan, benefits, and relocation assistance for new hires.

Servicios

Flexible compensation plan

Company benefits club

Relocation assistance

Formación

• University degree or equivalent in Biotechnology, Biochemistry, Biology, Chemistry, or related area.
• Master's degree in Chemistry, Biotechnology, Biochemistry, Biology, Chemistry, or related area.
• At least 4 years of experience in molecular biology and physico-chemical techniques.

Responsabilidades

• Generating necessary documentation related to reference materials (protocols, reports, certificates).
• Following up on the compliance of reference material analyses and reviewing stability study data records.
• Reviewing pharmacopoeia updates.

Conocimientos

Molecular biology techniques

Physico-chemical techniques

Pharmaceutical regulatory guidelines

High level of English (C1)

Educación

University degree in Biotechnology, Biochemistry, Biology, Chemistry

Master's degree in relevant area

Descripción del empleo

Are you looking for an opportunity to develop your professional career in a CDMO Quality Control department?

The successful candidate will join 3PBiovian, in Navarra, Spain, as part of our Quality Control department.

The candidate will be responsible for:

1. Generating necessary documentation related to reference materials (protocols, reports, certificates, etc.).
2. Following up on the compliance of reference material analyses and reviewing stability study data records.
3. Generating and reviewing raw material specifications.
4. Approving the status of materials for subsequent use in manufacturing.
5. Reviewing pharmacopoeia updates.

Assessment criteria:

• University degree or equivalent in Biotechnology, Biochemistry, Biology, Chemistry, or related area.
• Master's degree in Chemistry, Biotechnology, Biochemistry, Biology, Chemistry, or related area.
• High level of English (Level C1 / Advanced Certificate).

At least 4 years of experience in/with:

• Molecular biology and physico-chemical techniques specific to protein characterization.
• Recombinant proteins, mAbs, Biosimilars, ADCs.
• Pharmaceutical regulatory guidelines.

Why 3PBiovian?

Flexible compensation plan, allowing employees to allocate up to 30% of their gross annual salary to services exempt from income taxes (childcare, health insurance, academic training, etc.).

Company benefits club offering exclusive discounts on various products and services (Booking, FNAC, Rituals, El Corte Inglés, etc.).

Relocation assistance for new hires residing outside Navarra.

...And much more!

Why us?

We believe in passionate people with a shared purpose to manufacture advanced medicines.

We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian systems. We support our clients throughout their biologics journey, from development to delivery, offering process and analytical development, preclinical and clinical supply, and commercial production. Focused on biotechnology applications in human and animal health sectors, we provide tailored solutions to meet specific client needs.

As a leading global CDMO and preferred partner for pharmaceutical and biotech companies, we are committed to improving lives.