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Quality Technician in Villajoyosa

On-site in Villajoyosa·Added 29 days ago (last checked 15 Oct)

Agency

Michael Page España

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Our summary

Salary: €22,000 - €25,000 a year
About €1,500 - €1,650 a month after tax.
Work mode: On-site, Villajoyosa
Contract: Permanent
English: Required
Experience: 2+ years
Education: University degree

Visa options

The ad rules out sponsorship
The advert says visa sponsorship isn’t available for this role.

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Skills

Nice to have

Regulatory Affairs

Michael Page España is hiring for this role in several places. This vacancy is in Villajoyosa.

This job advert was originally written in Spanish.

Requirements

What we're looking for

Person with a university degree in Chemistry, Pharmacy, Biology, Biotechnology, or related health science areas.
Previous experience of at least 2 years in quality, highly valued within the pharmaceutical industry or in other regulated environments such as cosmetics, food, or medical devices.
High level of English (B2/C1) to interact regularly with international clients and suppliers.
Knowledge of GMP regulations, quality documentation management, audits, CAPAs, and deviations. Knowledge in Regulatory Affairs and chromatographic techniques will be valued.

Pay & benefits

What you'll get

Salary between €22,000 and €25,000 gross per year, with immediate start.
Professional development in a company with international projection and continuous training in GMP regulations.
Participation in international projects and audits with a high technical component within a collaborative and dynamic environment.

The role

You will be part of the Quality team, ensuring compliance with GMP regulations and the continuous improvement of processes in an international, innovative, and growing pharmaceutical company located in La Vila Joiosa (Alicante).

You will be part of the Quality team of a Pharmaceutical company.
International, innovative, and growing company, in La Vila Joiosa (Alicante)

What you'll do

Your main functions as a Quality Technician will be:

Participate in the planning, execution, and monitoring of audits for national and international clients and suppliers.
Review, update, and maintain the documentation of the GMP Quality System.
Manage deviations, corrective and preventive actions (CAPA), and change controls.
Monitor stability studies and perform documentary reviews of production and quality control processes.
Collaborate in qualification, validation, and monitoring of quality indicators (KPIs) activities.
Drive continuous improvement initiatives within the Quality Management System.

Hiring process

2 steps2 interviews

CV registration
Consultant contact
With a specialist Michael Page consultant
If they see that your experience and motivations fit the values and needs of a hiring company, they will contact you to start the selection process: they will learn about your expectations, answer your questions and help you prepare for each stage of the process.
Company interview
With a client company
If your application progresses, we will help you prepare for the interview with useful information about the company, its culture and what it looks for in a profile like yours.
Final stage and negotiation · With a client company

The final stages are set by the client company: Michael Page acts as an intermediary, and the interview and decision rest with the hiring company.
Support continues after the contract is signed.
Michael Page cannot support every candidate; registering and keeping your profile up to date opens the door to future processes.

About Michael Page España

Michael Page is a global recruitment consultancy and part of PageGroup, one of the world's leading professional recruitment firms. The company specializes in placing mid-to-senior level professionals across a wide range of sectors, including technology, engineering, finance, sales, and human resources. With a strong presence in Spain, Michael Page operates offices in major cities and offers services such as executive search, temporary staffing, and outsourcing solutions.

Industry: Staffing

In their own words

About the company & team

Our client is an innovative and growing pharmaceutical company, specialized in the development and manufacture of active pharmaceutical ingredients (API) under GMP regulations. With a strong international orientation, it stands out for its commitment to quality, continuous improvement, and compliance with the highest regulatory standards, collaborating with clients and suppliers at national and international levels from its facilities located in La Vila Joiosa (Alicante).

All open roles at Michael Page España