LIMS Technician - Quality Control

3PBIOVIAN; Noáin; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A leading biotechnology company in Spain seeks a LIMS Technician to improve workflows in the STARLIMS application for Quality Control. Responsibilities include user training, maintenance of analytical methods, and development of new functionalities. A degree in a related field and 3-4 years of relevant experience are required. Attractive benefits include flexible hours and a focus on employee well-being.

Servicios

26 paid days off

Flexible compensation plan

Company benefits club

Flexible working hours

Professional growth opportunities

Formación

• 3-4 years of experience in the biotechnology industry.
• Experience with laboratory computer applications.
• Knowledge of GMP regulations.

Responsabilidades

• Maintain and update analytical notebooks for Quality Control.
• Train users in the correct use of the application.
• Develop and validate new functionalities.

Conocimientos

GMP regulations

Biotechnology industry

Laboratory computer applications

Educación

University degree in Chemistry/Biology/Biochemistry/Pharmacy/Biotechnology

University master's degree in Computer Technology/Sample Management/Biomedicine

Descripción del empleo

The successful candidate will join 3PBiovian as a LIMS Technician - Quality Control.

Main responsibilities:

• Carry out improvements in the workflows already implemented in the STARLIMS application for the different management and analytical activities. In implementation stages in the Project Phase.
• Ensure the proper use in Routine of the system carried out by the Super Users for the control of the activities.
• Train the different users in the correct use of the application and its maintenance of the new activities developed in the project phase in the successive product expansions until its passage to routine.
• Participate in the development and validation of new functionalities.
• Write unit tests, drafting of the User SOP, drafting of the configuration SOP, of new functionalities to be implemented.
• Develop, maintain and update the generation of analytical notebooks (ELN) for analytical methods performed in Quality Control.
• Resolve incidents arising from the use of LIMS.

Assessment criteria:

• University degree or equivalent in related areas (Chemistry; Biology; Biochemistry; Pharmacy; Biotechnology, etc.).
• Valuable, university master's degree in related areas (Computer Technology; Sample Management; Biomedicine, etc.).

Between 3 and 4 years of experience in/with:

• GMP regulations.
• Biotechnology industry.
• Laboratory computer applications.
• Management and organization of electronic files and documentation.

️️Why 3PBiovian?

• You will have 26 paid days off: 23 vacation days + 2 personal days + 1 day off set by the company.
• Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income tax (childcare, health insurance, training, etc.).
• Company benefits club, which allows 3P employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, Fnac, Rituals, El Corte Inglés, etc.).
• Flexible working hours during the week and a reduce work day on Friday of 7h.
• Special Summer working day of 7h during July and August.
• 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees.
• The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust.
• We encourage the participation of our employees in solidarity events such as charity races, social donations...
• We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces.
• We have a high-impact work environment with flat hierarchies and short decision-making processes.
• All new hires who reside outside of Navarra are provided with a relocation service and/or assistance.

Why us?

We know it takes people with passion and 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 expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients

From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives.

It's within us.