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88,000+ live jobsTech Transfer Technician
On-site in Azuqueca de Henares·Added 2 days ago (last checked 15 Nov)
18 open roles
Our summary
- Hours
- Monday to Friday
- Work mode
- On-site, Azuqueca de Henares
- Contract
- Fixed-term
- Spanish
- Fluent
- English
- Required
- Education
- University degree
- Benefits
- Life insurance







Visa options
The ad rules out sponsorship
The advert says visa sponsorship isn’t available for this role.
Skills
This job advert was originally written in Spanish.
Requirements
What we're looking for
- Education: Degree or Bachelor's in Pharmacy or similar. Master's degree in the pharmaceutical field.
- Languages: Fluent Spanish and English; knowledge of other languages will be valued.
- Experience (years/area): at least 1-2 years of experience in a similar role, in formulation, production, or technology transfer in the pharmaceutical industry is highly valued.
- Specific knowledge: GMP, GLP, ICH, and FDA regulations and technology transfer procedures. Knowledge of formulation development (production equipment and processes), knowledge of regulatory affairs. Solid product knowledge.
- Personal skills: Ability to work both in a team and independently, dynamism, and multitasking.
Pay & benefits
What you'll get
Our benefits!
💸Attractive salary package depending on merit
🥼 Life and accident insurance
🍽️ Company canteen (free)
🥼 Co-payment on voluntary health insurance
💸Benefits and Savings Club
📈Development plans, internal mobility policy
⭐And much more!
The role
Position: Tech Transfer Technician - Injectables Plant
Experience: at least 1-2 years in the development of commented functions is highly valued
Location: Azuqueca de Henares
We are looking to hire a Tech Transfer Technician to join the team at our injectables pharmaceutical plant in Azuqueca de Henares.
The challenge!
Facilitate the transfer of pharmaceutical technologies from R&D or third parties to production, ensuring a seamless scale-up and regulatory compliance. The role includes evaluating potential new products and ensuring smooth technology transfers for successful industrialization.
What you'll do
- Work with manufacturing, quality assurance, quality control, regulatory affairs, and supply chain teams to ensure a smooth and efficient transfer. Support troubleshooting activities, investigate deviations, and contribute to continuous process improvement initiatives.
- Organize internal and client meetings to oversee project milestones, monitor execution, and report on progress.
- Issue MBR, BOM, and any other project-related documentation.
- Provide support during the manufacturing of registration/validation batches.
- Provide scientific and technical expertise, for example, in matters of quality, regulations, and technology transfer, and resolve day-to-day issues to ensure the flow of information between different functions and meet the project schedule.
- Verify that GMP document content is correct and complete and complies with the dossiers.
- Support product launches from the new site following the transfer, in collaboration with the commercial transfer team, supply chain, quality control, and regulatory affairs.
How you'll work
- Travel: Availability for occasional travel.
⏰Flexible schedule from Monday to Friday with entry from 08:00 to 09:30 and exit from 16:30 onwards depending on the entry time
📜Temporary contract due to production circumstances
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 about ensuring 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 experience 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 (Chemo), Branded (Exeltis), and Biotech (mAbxience), 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.
Additional information
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
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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