Alle Stellen für den Wiedereinstieg

Recipharm Advanced Bio, located in Cuxhaven, is a globally recognized partner for the development of the latest virotherapies and vector‑based vaccines. We develop manufacturing processes and produce oncolytic viruses for sustainable cancer treatment, gene therapies for genetic diseases, and innovative viral vector vaccines against fatal infectious diseases.

Recipharm Advanced Bio is part of Recipharm, a leading Contract Development and Manufacturing Organisation (CDMO) for the pharmaceutical industry. With over 5,200 employees worldwide, we provide manufacturing services for medicines in various dosage forms. In addition, the production of clinical trial material, active pharmaceutical ingredients, and pharmaceutical product development complement our portfolio.

As a contract manufacturer with project-based business, we work according to the principles of Good Manufacturing Practice (GMP). We serve customers in Europe, North America, and Asia and thereby support the development of highly innovative medicines. Our everyday work is highly varied and offers many development opportunities. We now want to reinforce our quality control department with a highly motivated colleague (m/w/d) in the framework of a maternity leave replacement.

Ihr Tätigkeitsfeld

• Support the head of quality control (HQC) in ensuring that Biopharmaceuticals, pharmaceuticals and other contracted products are tested in compliance with all applicable laws, regulations, standards, GMP guidelines and international guidelines.
• Assist in the development and manufacture of pharmaceutical products.
• Carry out release, stability, validation, verification and qualification testing for starting materials and finished products in accordance with current GMP guidelines.
• Document and evaluate test results.
• Maintain and calibrate laboratory equipment.
• Validate analytical methods.
• Create and edit test instructions and other related documents and procedures of quality control in agreement with the client (e.g., SOPs, qualification and maintenance documentation of laboratory equipment).
• Collaborate with interdisciplinary teams to optimise processes.
• Contribute to quality assurance measures within quality processes (e.g., D, CC, CP, OOS).

Ihre Qualifikationen

• Completed training as Technical Assistant (TA) in the fields of biology, chemistry or pharmacy, or comparable qualification.
• Experience in a pharmaceutical or biotechnological environment is an advantage.
• Knowledge of GMP or other certified quality management systems.
• Careful, structured working style with a strong focus on quality and hygiene awareness and organisational talent.
• Team player and strong communicator.
• Analytical thinking and problem‑solving competence.
• Very good German and English language skills in spoken and written form round out your profile.

Unser Angebot

• 2‑year fixed-term employment full‑time with the option of a permanent contract, 30 vacation days.
• An extremely varied workday.
• A family‑friendly company climate in an international environment.
• An attractive remuneration package.
• A company fitness programme, equity‑like benefits, bike leasing option.
• A company health insurance with health budget and many extra benefits.
• A mentoring programme for integration, etc.

Kontakt

Haben wir Ihr Interesse geweckt? Dann freuen wir uns über die Zusendung Ihrer aussagekräftigen Bewerbungsunterlagen.

Bei Fragen vorab erreichen Sie uns unter personal@vibalogics.com.

Seniority level

Entry level

Employment type

Contract

Job function

Management and Manufacturing

Industry

Pharmaceutical Manufacturing

Location: Cuxhaven, Lower Saxony, Germany