Job
- Level
- Experienced
- Location
- Reutlingen
- Working Model
- Onsite
- Job Field
- Project
- Employment Type
- Full Time
- Contract Type
- Permanent employment
Job Summary
In this position, you will independently plan and coordinate method validations and stability studies, conduct analytical testing, and communicate with internal and external partners on qualification projects.
Job Technologies
Your role in the team
- Independent planning and coordination of method validations, method transfers, and stability studies in consultation with the supervisor, including the preparation of plans and reports.
- Conducting analytical testing within the scope of method validations, method transfers, and stability studies.
- Participation in cross-departmental projects in the field of equipment qualification and computer system validation.
- Processing of quality-relevant processes (change procedures, CAPA, OOS, qualification of articles and suppliers) within the scope of responsibility.
- Communication with internal departments and external partners and service providers regarding qualification and validation projects.
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Our expectations of you
Education
- Completed Bachelor's or Master's degree in Biotechnology, Pharmacy, Chemistry, Biology, or a related field OR training as an MTA, MTLA, BTA, CTA, PTA with relevant professional experience.
Qualifications
- Analytical thinking and a structured, solution-oriented approach to work.
- Knowledge of relevant regulatory requirements, particularly ICH Q2 and ICH Q1, is desirable.
- Proficient handling of MS Word and Excel as well as good German and English skills.
- High self-motivation and enjoyment of interdisciplinary collaboration and communication.
Experience
- At least 2 years of professional experience in a GMP-regulated environment, ideally in the field of method validation or equipment qualification.
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What we offer
- Varied tasks - Work on innovative products in a company that truly makes a difference!
- GMP meets team spirit - Benefit from flat hierarchies and short decision-making paths.
- The best of both worlds - the advantages of a dynamic company with the security of an international group.
- Flexibility - Flexible working hours for many areas, and attractive shift models in the laboratory.
- Meaningful work with real impact - Your work directly contributes to shaping the medicine of tomorrow.
- Modern working environment - high-tech labs and innovative technologies for optimal working conditions.
- Opportunities for advancement - We support your further education and personal development.
- For your future - Company pension scheme for your long-term security.
- Corporate Benefits & Perks - Enjoy exclusive discounts and additional services.
- Sustainable commuting - Bicycle leasing offer for your commute to work.
- Conveniently located for work - Free parking for cars and bicycles right outside the door.
- Optimal location between Reutlingen, Tübingen in the beautiful Swabian Alps region, easily accessible and not far from Stuttgart.
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Topics You Will Work On
Job Locations
About Your Employer
TETEC AG
TETEC AG, based in Reutlingen, develops and manufactures innovative products in the field of tissue engineering and biomaterials. The company focuses on regenerative medicine, particularly for the treatment of cartilage damage and osteoarthritis. With a dedicated team of over 140 employees, TETEC works on personalized cell therapies and provides solutions for the human musculoskeletal system.
Description
- Company Type
- Established Company
- Working Model
- Onsite
- Industry
- Pharmaceutical Sector, Chemical Industry, Biotech
Project Manager - Method Validation & Qualification
- Location
- Reutlingen
- Working Model
- Onsite
- Diversity
- Open for all genders
