Qa engineer állások, munkák egészségügy, gyógyszeripar területen

• Minőségbiztosítás területén dokumentációs tevékenységek végzése, adatok feltöltése, kigyűjtése, elemzése, azok grafikus ábrázolása
• Értékelésekben történő részvétel
• Oktatási rendszer támogatása, tananyagok készítése
• Quality dokumentációk készítésében támogatás, fordítás

• Planning and initiation of business cases, definition of the project scope, objectives and deliverables. This includes gathering requirements, assessing feasibility and developing a project plan that aligns with organizational goals
• Monitoring of timelines and budget

QA Manager - Drug Product klinische Herstellung QA Manager - Drug Product Clinical Manufacturing (m/f/d) - Quality Assurance / Pharmaceutical / cGMP / Synthetic Molecules / GMP Audits / SAP / Veeva / German / English Project: For our client, a large pharmaceutical company based in Basel, we are...

Innovation/Design Control & Project Quality Engineer You can find all of our job offers by clicking here: /. Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics....

Global MSAT Quality Systems (QMS) Specialist Global MSAT Quality Systems (QMS) Specialist (m/f/d) : Quality Systems/ GMP Operations/ QMS/ CAPA/ Change Control/ MSAT/ Engineering Operations/ Pharma/ Veeva Vault/ Quality Docs/ LMS/ English Project: For our pharmaceutical customer based in Basel, we...

Scientist Quality Assurance (100%) INNOMEDICA IS A YOUNG NANOTECH COMPANY with around 40 employees, several promising drugs in preclinical and clinical development and its own clean room production. The pipeline is based on a liposomal delivery system and includes, in particular, parenteral drug...

• You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

Lead Expert Quality Assurance, Deputy Responsible Person 40% Become part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing...

Plan, Conduct, and Follow Up on Pharmacovigilance Audits including oversight and training of external service providers and consultants (for audits), ensuring adherence to company standards and regulatory requirements...

• Plan and Conduct GCP Audits: Develop a risk-based audit schedule covering all relevant areas, including investigator sites, vendors, and internal processes, to ensure adherence to GCP guidelines
• Oversee Corrective and Preventive Actions (CAPA) specific to GCP (internal or external)

Following up on production-related nonconformities, supporting root cause analyses, defining and monitoring corrective actions, and preparing evaluations and statistics of nonconformities...

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