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87,000+ live jobsSecondary Packaging Material Quality Control Analyst
On-site in Azuqueca de Henares·Added 11 days ago (last checked 2 Nov)
61 open roles
Our summary
- Hours
- Rotating shifts, including nights · Monday to Friday
- Contract
- Permanent
- Benefits
- Life insurance



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
✔ Vocational Training or equivalent in Pharmacy, Chemistry, Biology, Health Sciences, or similar.
✔ Solid experience in a GMP environment and knowledge of associated documentation and requirements.
✔ Knowledge in material sampling, AQL inspection, document review, and release processes.
✔ Methodical, rigorous profile, with attention to detail and orientation toward regulatory compliance.
Nice to have
✔ Valued experience in supplier management and packaging materials/medical devices.
Pay & benefits
What you'll get
⏰Rotating shift: mornings 06:00 to 14:00, afternoons 14:00 to 22:00, and nights 22:00 to 06:00 (Monday to Friday)
📜Permanent contract
💸Salary based on merit (fixed salary + rotation bonus + night shift bonus)
🥼 Life and accident insurance.
🥼 Co-payment for voluntary health insurance.
💸Benefits and Savings Club.
📈Development plans, internal mobility policy.
The role
Position: Secondary Packaging Material Analyst
Location: Azuqueca de Henares
Experience: at least 2 years in similar roles
What you'll do
· Execution and recording of sampling activities for Direct Materials (API, excipients, and packaging material).
· Physical and IT maintenance of the sampling room.
· Physical and IT maintenance of the documentation archive.
· Physical and IT maintenance of the sample library.
· Inspection by attributes (AQL) of primary and secondary packaging materials.
· Execution of testing for different water qualities and secondary packaging materials.
· Monitoring of the documentation established for the execution of tasks in the Laboratory (standard operating procedures, supporting documentation, manuals, etc.) and GxP work systematics.
· Contribution to guaranteeing the state of training control required in their area of responsibility (specific technique, GxP, safety, etc.).
· Collaboration for the correct development of GMP regulatory inspections, customer audits, and the execution of the self-inspection program.
· Collaboration in maintaining the proper state of order and cleanliness of the Laboratory.
What do you need?
Our benefits!
⭐And many more!
What will the Selection process be like? 🕵️
Follow us on social networks such as LinkedIn/Instagram and stay tuned to any offers we release; the opportunity to be a new Insuder is waiting!
#InsudPharma #Challenger #Insuder #InsudTalent
Hiring process
➡️Keep an eye on your phone and email! Most likely, the first thing we will do is contact you through one of those two channels.
➡️Prepare well! We will continue with an in-person/virtual interview depending on availability and agreement; there may be between one and two interviews in the process and, depending on the type of process, there may also be some type of test.
➡️Wait for the result! We care that you feel guided in every selection process and know what to expect from us, so we will endeavor to always indicate the status of the process to you.
About Insud Pharma
- Industry
- Pharmaceuticals
In their own words
About the company & team
INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and expertise in scientific research, development, manufacturing, sale, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health.
INSUD PHARMA's activity is organized into three synergistic business areas: Industrial, Branded, and Biotech, with more than 10,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development.
We are incorporating a new INSUDER as a Secondary Packaging Material Analyst in our injectables plant located in Azuqueca de Henares.
The challenge!
To guarantee the correct execution of sampling activities and basic laboratory analysis, and the monitoring of applicable regulations and procedures to ensure the full development of their work activity in a GxP environment.
Additional information
The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as set out in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.
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