QA Manager 100% (w/m/d)
Introduction
Established in 1836, Acino, part of Arcera, is a pharmaceutical company headquartered in Zurich, with a clear focus on selected markets in the Middle East, Africa, and Latin America, as well as Ukraine and Eurasian countries. With over 3,000 people across 90 countries, we deliver quality pharmaceuticals to promote affordable healthcare in these emerging markets. We also leverage our high-quality pharmaceutical manufacturing capabilities and network to supply leading companies through contract manufacturing and out-licensing.
Acino is part of Arcera, a diversified life sciences holding company, established by ADQ in Abu Dhabi in 2024 with the purpose to advance innovation in line with the Emirate’s 2030 vision for the sector and beyond.
We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our team in Munich, Germany.
QA Manager 100% (w/m/d)
Major Accountabilities:
Review and approval of GMP and GDP related documents (e.g. MBRs, Certificates of Analysis, deviations, artworks)
Support of the Qualified Person (QP) in batch release preparation, including document provision, review, and preparation, batch record review, as well as maintenance and continuous improvement of related systems.
Management, coordination and follow-up of change controls, complaints, deviations, CAPAs and Events in the eQMS, ensuring timely completion and GMP-compliant execution
Continuously drive improvement of our quality assurance systems
Review and update of documents (e.g. SOPs, certificates of analysis, specifications, SMF)
Represent the company in inspections by authorities and provide support as well as follow-up of observations
Responsible for the archiving of documents as well as for the storage and management of retained samples
Support other team members as required
Compile and lead communication with suppliers and service providers
Support in administrative and organizational activities
Administration of the GMP training in electronic learning management system
Coordination, preparation, and review of Product Quality Reviews (PQRs)
Your Profile:
Master’s degree in Life Science, preferably in Pharmacy or Pharmaceutical Sciences
3-5 years of experience in pharmaceutical industry preferably in Quality Assurance or Quality Management
Excellent planning and organizational skills with capability to prioritize tasks and adhere to timelines highly required
Prompt and accurate performance of tasks and responsibilities
Structured and quality-conscious way of working
Able to work in an international and interdisciplinary environment
Team player with good communication and negotiation skills
Target oriented, multi-tasking and able to work under pressure
Fluent in German and English, with excellent written and verbal communication skills
You can expect the following benefits:
We offer a very attractive working environment within a highly motivated team with excellent working conditions.
A position with a stable and resilient pharmaceutical company
An international working environment within a continuously growing organization
Interesting and highly diverse responsibilities that provide a strong foundation for further career development in the pharmaceutical industry
An attractive salary package
Complimentary coffee, tea, and fresh fruit
Attractive additional benefits, such as corporate benefit programs
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future.
Contact
If you are interested in this role we are looking forward to hearing from you.
Please apply via our HR system here.
Note that only direct applications via our HR system (follow the link above) will be considered.