€50k - €55k
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92,000+ live jobsQA Technician | Validations
On-site in Arganda del Rey·Added 1 month ago (last checked 26 Oct)
Our summary
- Salary
- €35,000 - €37,000 a year
About €2,200 - €2,310 a month after tax.
- Hours
- Rotating shifts, including nights
- Work mode
- On-site, Arganda del Rey
- Contract
- Permanent
- English
- Required
- Education
- University degree






Visa options
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
Skills
This job advert was originally written in Spanish.
Requirements
What we're looking for
Degree in Pharmacy, Chemistry, Biology, Biotechnology or similar.
Experience in QA operations within the pharmaceutical industry, manufacturing environments, quality, layers. Essential.
Professional level of English.
Open to working rotating shifts: morning, afternoon and night.
Be a professional with great passion!
Pay & benefits
What you'll get
- Immediate start.
- Dynamic and quality-oriented environment.
- Culture of continuous improvement and innovation.
- Opportunity to have a direct impact on daily operations.
- Attractive competitive compensation package + interesting benefits
If you are interested, or know someone, do not hesitate to contact me!
The role
Important and leading company in the pharmaceutical sector dedicated to the manufacturing of products under GMP standards, with a strong focus on quality, innovation, and continuous improvement.
- Major leading company
- Permanent Position as Operational Quality Assurance Technician
What you'll do
As part of the team, you will be responsible for the following duties:
- Production during softgel capsule manufacturing operations.
- Review and approval of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
- Supervision of GMP compliance in production areas, including encapsulation, drying, inspection, and packaging.
- Management and follow-up of deviations, CAPAs, and change controls.
- Define and coordinate appropriate corrective and preventive actions in collaboration with Production and other departments.
- Support investigations and root cause analyses related to manufacturing incidents.
- Review and approval of SOPs, protocols, reports, and quality documentation.
- Participate in risk assessments and continuous improvement initiatives.
Hiring process
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
Important and leading company in the pharmaceutical sector dedicated to the manufacturing of products under GMP standards, with a strong focus on quality, innovation, and continuous improvement.




