Quality Assurance Specialist (all genders) fixed-term 2 years

Stellenbeschreibung:

At Bayer we work to solve the world’s toughest challenges and strive for a world where health for all and hunger for none is no longer a dream, but a real possibility.

Quality Assurance Specialist (all genders) - fixed‑term 2 years

As a Quality Assurance Specialist, you ensure GMP‑compliant manufacturing of pharmaceutical products and make a significant contribution to the quality and compliance of modern production processes. Leveraging your pharmaceutical expertise, you work closely with Production, QA, and QC teams to ensure that the highest quality standards are consistently maintained and continuously improved in daily operations.

Your Tasks and Responsibilities

You will oversee pharmaceutical production facilities for the manufacture of parenteral products.
In doing so, you will ensure that manufacturing processes are carried out in accordance with GMP guidelines and recognized pharmaceutical regulations.
You will regularly create and update pharmaceutical‑related documents (e.g., manufacturing instructions in accordance with Section 13 AMWHV, SOPs).
In the event of process deviations, you will prepare investigation reports in coordination with QA/QC.
You will ensure that necessary validations of manufacturing processes are carried out, as well as required initial and ongoing training for production staff (12 AMWHV), and initiate measures within the scope of Change Control when necessary changes are required.
You review manufacturing records, handle complaints, and manage the preparation and follow‑up of inspections and audits.
Within the scope of projects and processes, you ensure GMP compliance and optimize it with a view to cost‑effectiveness.
Supervising the practical training of pharmacy interns (4 AappO) is also part of your responsibilities.

WHO YOU ARE

You have a degree in pharmacy and are licensed as a pharmacist.
Ideally, you have gained initial professional experience in the pharmaceutical industry in the areas of manufacturing, testing, and evaluating medicinal products.
You possess a strong understanding of drug risk assessment as well as national and international regulations (pharmaceutical law) and are confident working in a GMP environment.
You are proficient in IT systems such as MS Office.
You have the ability to analyze technical processes, derive targeted measures, and think holistically.
You possess strong organizational skills and excellent communication skills.
You are distinguished by leadership qualities such as the ability to work independently, assertiveness, communication skills, flexibility, and resilience.
You have a strong focus on quality and cost awareness.
Fluency in German and good written and spoken English round out your profile.

Additional Information

The position is a 24‑month fixed‑term contract.

What We Offer

Competitive salary between 77.300€ and 93.800€ per year (full‑time) plus a variable component.
Flexible work models or part‑time arrangements.
Family support services (company daycare centers, childcare support, time off for caring for elderly or dependent family members, summer camps for children).
Professional growth through learning and development opportunities, training programs, development dialogues, coaching and mentoring programs.
Health awareness and self‑care opportunities, such as free health checks with the company doctor.
Inclusive work environment embracing diversity.

Equal Opportunity Statement

Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.