We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department.
Por favor, presente su candidatura sin demora si su perfil encaja bien con este puesto, debido al alto nivel de interés.
Responsibilities
Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader.
Ensure the correct training of the personnel in charge.
Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms.
Participate in internal / external audits as required by the Quality Assurance Department.
Comply and ensure compliance with GMP standards within the work team.
Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB).
Investigate and propose new methods or process innovations to optimize and improve the work in the area.
Ensure proper compliance with regulations and correct completion of current documentation.
Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager.
Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB).
Supervise the correct completion of the new equipment entry documentation.
Supervise the correct training of the personnel in charge, if any.
Carry out the distribution and supervision of daily activities.
Write and keep updated the documentation associated with the production processes carried out in the USP area.
Control / monitoring of orders placed in the USP production area using ERP software.
Assessment Criteria
Education:
Bachelor's degree in Pharmacy;
Biology;
Biochemistry;
Biotechnology;
Chemistry;
IPPA;
Chemical Engineering, cell culture etc. Desirable but not required Master's degree or equivalent in related fields.
Languages:
Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate).
Experience (1-2 years):
GMP/GLP regulations
Industrial‑scale bioreactors
Cell Cultures
Microbiological analysis techniques
Upstream production positions
Biotechnology / Biopharmaceutical Sector
Other requirements:
Open to work in shifts.
Software package: Office. User level.
Benefits
A permanent and stable position in a competitive growing company.
A competitive time off package with 41 paid days of vacation.
Versátil compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.).
All new hires who reside outside Navarra are provided with a relocation service and/or assistance.
Company benefits club, which allows employees to obtain exclusive prices and discounts on a multitude of products and services.
Learning & Development department creates personalized, individualized and differentiating career plans for employees.
Focus on internal talent and stable employment, focusing on upskilling and reskilling.
Participation in solidarity events such as charity races, social donations.
Programs aimed at improving physical, psychological and emotional well‑being, including Corporate Challenge, healthy lunches and comfortable and safe work spaces. xhfqzwm
High‑impact work environment with flat hierarchies and short decision‑making processes.
#J-18808-Ljbffr