Ormaiztegi Biological & Biomedical Sciences Job Listings

Quality Control Technician64870739704449120

Indeed

Quality Control Technician

We are seeking a candidate with experience for a Quality Control Technician position at a chemical industry company in Andoain. Your responsibilities will include daily verification of quality standards in the laboratory, ensuring full compliance with regulatory requirements. You will also be responsible for supervising and controlling the quality of products received from suppliers. In addition, you will carry out administrative tasks related to the Quality Department, as well as part homologation and process certification according to ISO standards, among other duties inherent to the position. A full-time work schedule of 40 hours per week is offered, distributed from Monday to Friday, with legally mandated breaks. * Prior experience in a position equal to or similar to the one described. * We seek a proactive and dynamic individual. * Proximity of residence to the workplace is valued. GM/GS related to the vacancy.

Lugar, 235X, 20140 Andoain, Gipuzkoa, Spain

Negotiable Salary

Indeed

Cleaner

We are seeking personnel to perform cleaning tasks in various facilities, such as buildings, offices, or premises, as well as common areas. Previous experience in cleaning duties and knowledge of cleaning chemicals and supplies will be considered an advantage. Main responsibilities include cleaning floors, ceilings, walls, and furniture in the interior areas of the facilities. Working hours may be full-time or part-time, Monday through Friday, with half-day shifts from 09:00 to 13:00 or full-day shifts from 15:00 to 21:00. A permanent contract is offered.

Kalea Valle Donibanealde, 13Z, 20100, Gipuzkoa, Spain

Negotiable Salary

Indeed

Production Technicians

**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is based on honesty, excellence, leadership, involvement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization) and **the trust placed in us by more than 40 biotechnology companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for the treatment of various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking **Production Technicians** to perform this key function reporting directly to the Production Manager (USP/DSP). **You will carry out lentiviral vector production processes according to manufacturing guideline instructions under GMP regulations.** To achieve this, you will be part of a team where you will propose improvements, draft manufacturing protocols, standard operating procedures (SOPs), and other relevant documentation related to manufacturing. ### **Your responsibilities** * Carry out lentiviral vector production processes according to manufacturing guideline instructions under GMP regulations. * Draft manufacturing protocols, standard operating procedures (SOPs), and other relevant manufacturing-related documents. * Comply with and ensure compliance with internal production standards. * Be part of a multidisciplinary team to conduct process optimizations and investigations. * Perform maintenance of production areas to ensure their condition and compliance with GMP regulations. ### **What we value in you** You are who we are looking for if you have: * A degree related to biomedical research (Sciences, Biology, Biochemistry, Chemistry, Pharmacy…) or related engineering. * Higher-level qualification related to the field. * Previous experience in production within GMP environments and/or bioprocesses will be positively valued. * Ability to suggest potential process improvements and tests. * Competent verbal and written communication skills in Spanish and English. * Ability to work in a team and meet deadlines. * Residence in Gipuzkoa (or intention to relocate to the area) will be positively considered. ### **We offer you** * You will have continuous career development opportunities that will help you grow your talent throughout your professional journey. * You will participate in innovative projects with constant technological updates. * You will receive a competitive salary commensurate with your profile for this position. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support you during your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (accommodation, job placement for family members, school enrollment, ...). * You will enjoy a professional work environment that truly stands out due to our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals receive equal consideration for our open positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia / San Sebastián, Gipuzkoa, Spain

Negotiable Salary

Embryologist in Vitoria - Part-time64147587663490123

Indeed

Embryologist in Vitoria - Part-time

At Next Clinics, one of the leading assisted reproduction companies in Europe, we are looking for an Embryologist for our clinic in Vitoria. As an Embryologist, your role will involve handling gametes from patients and donors to ensure the highest success rates in our assisted reproduction treatments. **What do we offer?** * 6-month contract * Part-time schedule of 20 hours/week * Continuous training **What will your responsibilities be?** * Preparation and control of culture media * Oocyte denudation * Cryopreservation and thawing of gametes and embryos * Monitoring of embryonic development * IVF, ICSI and embryo transfer * Performing embryonic biopsies * Maintenance and updating of records and related documentation **What requirements must you meet?** * University degree in Biology, Pharmacy, Medicine, Chemistry, Biochemistry or Veterinary Science with a Master’s in Human Reproduction. * At least 1 year of experience in Assisted Reproduction * Availability to perform on-call duties * Attention to detail and organizational skills * Problem-solving ability and proactivity * Advanced level of English, Italian, French, German or Dutch (other languages will be an advantage) If you believe this opportunity is right for you, apply now—we will review your application as soon as possible.

c, Laserna, 1, 01015 Vitoria-Gasteiz, Araba, Spain

Negotiable Salary

Senior Occupational Health and Safety Technician64146425993987124

Indeed

Senior Occupational Health and Safety Technician

Do you have solid experience in Industrial Hygiene and are you looking for a new professional challenge where you can lead, analyze, and improve working conditions from a technical and strategic perspective? At **EUROPREVEN**, we are seeking a **Senior PRL Technician** with experience in **Industrial Hygiene** to join our prevention team on a long-term project. **Your main responsibilities will be:** Industrial Hygiene Area: * Review and evaluation of **chemical products**, safety data sheets (SDS), and labeling. * Analysis and characterization of **workstations exposed to chemical, physical, or biological agents**. * Conducting **hygienic measurements**, sample collection, and data analysis. * Preparation of **technical reports and specific hygiene risk assessments**. * Definition of preventive and corrective measures based on results. * Monitoring exposure to contaminants and assessing the effectiveness of implemented measures. Comprehensive Prevention Management: ️ * Active participation in **planning preventive activities**. * Assessment of general and specific occupational risks. * Proposal and implementation of continuous improvements in safety and hygiene. * Collaboration with the rest of the technical team in preventive campaigns. * Direct support and advice to various departments and area managers. **Essential requirements:** * **Master's degree in Occupational Risk Prevention**, covering all three specialties. * Minimum of **2\-3 years** of experience in similar roles. * Strong analytical skills and ability to prepare rigorous technical reports. * **Responsible, committed, methodical professional with a proactive prevention mindset.** * Class B driver's license and **own vehicle**. What we offer: * **Permanent contract**. * Competitive salary: **30\.000€ gross annual**. * Working hours from Monday to Friday (8:00 AM to 5:00 PM). * Positive work environment, autonomy, and professional development. **Location**: Durango **Immediate incorporation**If you are looking for a new professional challenge in the field of Industrial Hygiene and want to contribute your expertise in an environment where your knowledge will make a difference, **EUROPREVEN is waiting for you.**

Biscay, Spain

€ 30,000/year

QUALITY, PROCESSES AND/OR ENVIRONMENTAL MANAGEMENT SYSTEMS CONSULTANT64146420077955125

Indeed

QUALITY, PROCESSES AND/OR ENVIRONMENTAL MANAGEMENT SYSTEMS CONSULTANT

Donostia · Published on 2025\-10\-02 COMPANY DESCRIPTION GRUPO GISMA is a consulting firm with a long-standing track record, founded 27 years ago. Currently, we specialize in ISO STANDARDS, PEOPLE, STRATEGY\-INNOVATION. Our purpose is to make companies more consistent and sustainable. We are a company in constant evolution and are currently undergoing a growth phase. Therefore, we need a QUALITY, PROCESSES AND/OR ENVIRONMENTAL MANAGEMENT SYSTEMS CONSULTANT. POSITION DESCRIPTION \+ RESPONSIBILITIES Do you enjoy challenges and find satisfaction in helping companies implement quality and/or environmental management systems that enhance consistency and sustainability? Can you add value in implementing quality and/or environmental management system projects? We are looking for experienced professionals to lead quality management system projects with clients, focusing on closeness, collaboration, adaptability, efficiency, and value creation. Under the supervision of the Department Manager, your responsibilities will include: * Advising and implementing Quality Management Systems (9001, 45001,) and Environmental Management Systems (14001,14006\...). * Accompanying clients, identifying their needs, and providing solutions that ensure their sustainability. * Delivering training courses on any of the above topics to client companies. * Advising client companies during external audits of Quality and Environmental Management Systems. MINIMUM JOB REQUIREMENTS The most important qualities for our team are responsibility, approachability, collaboration, adaptability to change, and integrity\*\*.\*\* * Education: Degree in Engineering, Chemistry, Biology, Business Administration, or Higher Vocational Training related to quality and environment. * More than 3 years of experience in the previously mentioned functions, either in consultancy or within a company. * Knowledge: ISO 9001, 14001\. Microsoft Office * Strong planning and organizational skills to manage multiple projects simultaneously. * Valid driver's license and access to personal vehicle. **Desirable qualifications:** * Spoken and written Basque (Euskera) * Knowledge of other Standards: ISO 45001, 3834, 15085, 27001, ... * Broad business vision. * Report writing and documentation skills. * Experience using any ERP system. * Knowledge of AI. WHY WORK WITH US? * Flexibility: Flexibility is one of GRUPO GISMA's key characteristics. We work on a project basis, which functions effectively when employees respect quality standards and agreed deadlines with clients. * Telecommuting: We are flexible. To foster relationships, communication among team members, and better integration of new staff, we encourage working from the office one or two days per week. * Development: We support your professional development. Integration plan and annual development plan. If you lack experience in implementing certain Standards, our team will train you. * Holidays: We close for two weeks in August; you can schedule the rest of your vacation time as you wish. * Other benefits: Mileage and daily allowances, company phone and laptop. * Team: You will join a passionate and dedicated team who will welcome you from day one and support your professional growth. * Certifications: We hold various certifications in Quality, Equality, Work\-Life Balance, and Bai Euskarari. Our carbon footprint is calculated and registered. We are listed in the Basque Cybersecurity Centre catalog. ARE YOU THE PERSON WE'RE LOOKING FOR? DON'T HESITATE—APPLY! WE'RE WAITING FOR YOU Apply for this position Details Location Guipúzcoa Sector Consulting Work mode Hybrid Contract type Permanent Working hours Full\-time Share this job offer GRUPO GISMA Job offers

San Martin Kalea, 31, 20005 Donostia, Gipuzkoa, Spain

Negotiable Salary

Biology Teacher in English (ESO/Bachillerato). Part-time. CEU Virgen Niña School Vitoria63841288999043126

Indeed

Biology Teacher in English (ESO/Bachillerato). Part-time. CEU Virgen Niña School Vitoria

From the CEU Virgen Niña School in Vitoria, we need to hire a teacher to teach Biology in English and Physics and Chemistry in ESO and Bachillerato. Requirements:* Degree in Biology, Chemistry, Biochemistry or similar. * Advanced level of English. * Master's in Teacher Training. Responsibilities: Educate students in the respective subjects, promote positive coexistence both inside and outside the classroom, set learning objectives and assess the progress of acquired knowledge, with the aim that students receive a high-quality education at CEU schools and have a satisfactory academic experience

Calle la Esperanza, 19, 01002 Vitoria-Gasteiz, Araba, Spain

Negotiable Salary

Business Development Managers63840025114881127

Indeed

Business Development Managers

**About us** ------------------ We are a CDMO (Contract Development and Manufacturing Organization), and the trust placed in us by more than 40 biotechnology companies worldwide is our best endorsement. We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for the treatment of various diseases, including hematological and solid cancers, as well as rare diseases. **We're looking for you to join our Team!** ### **Your role** We are seeking **Business Development Managers**, reporting to the Head of Business Development, with experience in this function, whose main mission will be to identify and generate new business opportunities for the company, aiming to convert them into new contracts for the organization. Likewise, they will support negotiations with clients on some of the emerging opportunities when required. ### **Your responsibilities** * Identify and generate new opportunities from clients interested in VIVEbiotech's services, with the ultimate goal of converting these into new contracts and achieving the Annual Sales Plan. * Continuously follow up on VIVEbiotech’s portfolio of potential clients through regular re-contacts using different formats, aiming to uncover new opportunities. * Prepare and attend meetings with clients at VIVEbiotech or at the client's premises, highlighting the distinctive features of the company's services and products, and adapting effectively to each client's specific needs. * If required, participate in certain negotiation processes with our clients. * Adequately understand VIVEbiotech's market, including potential clients, competitors, and technological partners, among others, to successfully perform the duties of a business development technician. * As required, prepare and attend several international sector-specific events per year to expand and strengthen VIVEbiotech’s current client portfolio. * Align with VIVE culture both within and outside your team: teamwork, behavioral values, customer orientation, and continuous improvement in quality, safety, and environment are essential to becoming part of the VIVEbiotech team. * Proactively provide ideas for continuous improvement in cost-effectiveness related to your knowledge, experience, and execution of your role, contributing to the achievement of your team or department’s objectives. * Report any significant issues affecting the smooth progress of your activities or those of your team or department to your direct supervisor. * Carry out your job responsibilities while respecting the company's cultural values both within and outside your team. Key work behaviors include: + Teamwork, with proactive collaboration and mutual support among colleagues, performing necessary cross-functional tasks within your department to ensure successful team or department outcomes. + Customer orientation, responding flexibly to emerging needs. + Working with a mindset of continuous improvement regarding the quality of your tasks, workplace health and safety, and environmental impact, particularly within your team or department and across the company in general. ### **What we value in you** You are who we’re looking for if you have: * University degree in Molecular Biology, Biotechnology, Biomedicine, Pharmacy, etc. A Master’s degree or PhD thesis will be positively considered. * Excellent command of English, strong internal and external communication skills, both verbal and written. * Scientific-technical background enabling effective interaction with VIVEbiotech's type of clients. * At least 1 year of experience in sales/business development within the pharmaceutical/biotech industry, preferably in the CDMO sector. * Outstanding communication ability. * Experience in negotiation, sales, market analysis, technology monitoring, etc. * Experience conducting international travel and attending trade fairs and congresses. * Ability to continuously learn, with a process improvement mindset, and proactivity in problem-solving and proposing improvements. * Rigor and autonomy, as well as flexibility and capacity to work quickly and accurately, with a clear customer focus and commitment to high-quality standards. * Teamwork skills and a positive attitude toward change. ### **What we offer** * You will have access to continuous career development that supports nurturing your talent throughout your professional journey. * You will participate in innovative projects undergoing constant technological updates. * You will receive a competitive salary aligned with your profile for this position. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing disease cures. * We will support your personal relocation process if you come from another region and wish to move to Donostia-San Sebastián (accommodation, job placement for family members, school enrollment, etc.). * You will enjoy a professional working environment truly distinguished by our humanity and closeness, where diversity and inclusion are valued. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals are equally considered for our open positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary

QA Technician Manufacturing63840025096705128

Indeed

QA Technician Manufacturing

**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is built on honesty, excellence, leadership, engagement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization) and **the trust placed in us by more than 40 biotech companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for the treatment of various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking a **QA Technician Manufacturing** to fill this key position reporting directly to the Department Manager. Your mission will be **to ensure that necessary activities are carried out within the company to comply with applicable “Regulatory Requirements” and the “Quality Management System” in Manufacturing and Quality Control activities.** Similarly, you will provide **active support in continuous improvement of the quality system and in the implementation of new computerized systems and technologies for the overall enhancement of VIVE’s Quality area.** ### **Your responsibilities** * Manage the execution of the Quality Management System: Change Controls, corrective and preventive actions (CAPAs), risk assessments… * Manage GMP documentation: Standard Operating Procedures, Master Formulas, Analytical Methods… * Provide active support in the implementation of new computerized systems in the Quality area (ERP, Document Management, and management of Change Controls, Deviations, and CAPAs). * Review and approve the execution of manufacturing instructions and analytical techniques. * Support the execution of projects: product development, process validations, and preparation of reports. * Support audit execution. * Comply with VIVE's safety regulations and contribute to their continuous improvement by reporting incidents from your own area or any other part of the company if detected. ### **What we value in you** You are who we are looking for, if you have: * Studies related to Pharmacy, Biotechnology, Biology, Biochemistry, etc., complemented with knowledge of Regulatory Compliance (GMP, etc.) * Training in Good Manufacturing Practices: EMA and FDA * Previous experience in the pharmaceutical industry in similar roles, with certification in Good Manufacturing Practices. * Experience in risk analysis and management, as well as in the use of computerized systems applied to the pharmaceutical industry will be valued. * Additionally, you are a person oriented toward high quality (excellence and self-demand), organized and orderly. * You proactively provide ideas for continuous improvement and offer your knowledge and experience to help achieve your Department's objectives. * Ability to work effectively within a team and you are proactive. * You are responsible and rigorous in your work, demonstrating high work capacity when there is high demand for results and deadlines. * You always demonstrate a positive attitude towards change. * Residence in Gipuzkoa (or intention to relocate to the area) will be positively considered. ### **We offer you** * You will have continuous career development that will help you grow your talent throughout your professional journey. * You will participate in innovative projects undergoing constant technological updates. * You will receive a competitive salary commensurate with your profile for this position. * You will have flexible working hours, with the support needed to balance your personal and professional life. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (accommodation, job placement for family members, school enrollment, …). * You will enjoy a professional work environment truly distinguished by our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals receive equal consideration for our open positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary

DSP Production Technicians63840025079555129

Indeed

DSP Production Technicians

**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is based on honesty, excellence, leadership, engagement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization) and **the trust placed in us by more than 40 biotech companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for the treatment of various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking **DSP Production Technicians** to perform this key role directly reporting to the DSP Production Manager. **You will carry out lentiviral vector production processes according to manufacturing guidelines under GMP regulations.** To achieve this, you will be part of a team where you will propose improvements, draft manufacturing protocols, standard operating procedures (SOPs), and other relevant documentation related to manufacturing. ### **Your responsibilities** * Carry out lentiviral vector production processes according to manufacturing guideline instructions under GMP regulations. * Draft manufacturing protocols, standard operating procedures (SOPs), and other relevant manufacturing-related documents. * Comply with and ensure compliance with internal production standards. * Be part of a multidisciplinary team to conduct process optimizations and investigations. * Perform maintenance of production areas to ensure their condition and compliance with GMP regulations. ### **What we value in you** You are who we are looking for if you have: * Degree related to biomedical research (Sciences, Biology, Biochemistry, Chemistry, Pharmacy…) or related engineering. * Higher vocational qualification related to the field. * Previous experience in production within GMP environments and/or bioprocesses will be positively considered. * Ability to suggest potential process improvements and testing. * Competent verbal and written communication skills in Spanish and English. * Ability to work in a team and meet deadlines. * Residence in Gipuzkoa (or intention to relocate to the area) will be positively valued. ### **What we offer** * You will have continuous career development opportunities that will help you grow your talent throughout your professional journey. * You will participate in innovative projects with constant technological updates. * You will receive a competitive salary commensurate with your profile for this position. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support you in your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (housing, job placement for family members, school enrollment, etc.). * You will enjoy a professional work environment truly distinguished by our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals receive equal consideration for our vacant positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary