Process Documents Jobs in Bergisch Gladbach

Als Business Process Manager sind Sie eine wichtige Sttze fr die Prozessverantwortlichen mit Ihrer Expertise beraten Sie sie bei der Erstellung von effizienten Prozessen die den Erfolg des Unternehmens nachhaltig sichern.Sie erreichen mit den Prozessverantwortlichen optimale Ergebnis More...

As Senior Manager Process Development at Miltenyi Bioindustry you will lead a group driving the technical development of cells and vectors for our customers. The focus is on cell and gene therapy as well as lentiviral vector services implemented on our advanced inhouse platforms e.g. More...

Supporting customer projects with a focus on the area of Sales & Distribution/Material Management.Support in all project phases from conception design customising and prototypes to rollout. to the roll out.Consulting our customers in the environment of implementation and migratio More...

 Within our R&D Reagents department you are supporting the hematopoietic stem cell (HSC) engineering team.You are responsible for the planning implementation and execution of projects focusing on GMPcompliant processes using the CliniMACS Prodigy platform.You plan and carry o More...

You primarily support S/4 Hana transformation projects in the life science chemicals and food production industries with a focus on the area of (embedded) extended warehouse management.Furthermore you support all project phases from conception design customising and prototypes to rol More...

Analyzing of the customer situation creating process documents concepts and blueprints with a focus on SAP financial modules (FI AA CO CA IM TR BPC).Responsibility for the systemside realization of customer requirements (customizing coordination of addons user exits developm More...

Analyzing of the customer situation creating process documents concepts and blueprints with a focus on SAP financial modules (FI AA CO CA IM TR BPC)Responsibility for the systemside realization of customer requirements (customizing coordination of addons user exits development of repo More...

In your role as a Regulatory Affairs Manager you will be involved in the development of ATMPs.You will support the Regulatory Affairs department in preparing and reviewing approval documents for our products in cell and gene therapy.You will compile dossiers and take care of the submi More...

In your role as a Regulatory Affairs Manager you will be involved in the development of ATMPs.You will support the Regulatory Affairs department in preparing and reviewing approval documents for our products in cell and gene therapy.You will compile dossiers and take care of the submi More...

You will join our team responsible for the postmarket surveillance (PMS) of our clinical products (medical devices in vitro diagnostics and GMP products) and perform organizational and administrative tasks to manage PMS data.    You will be responsible for the mana More...

In the Clinical Trial Execution Service department you will support our study processes and activities in line with our gotomarket strategy for investigational medicinal products (IMPs) particularly in haematological and oncological indications. You will be the expert and first point More...

In this role you will be responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP) E6 ICH Guidelines and other regulatory guidance documents and Clinical Trials Regulati More...

Job Description Tasks Coordination and oversight of all tasks related to type Investigation in concurrence with internal stakeholders and the competent authority Advising of all departments of the design organisation in all questions regarding airworthiness operational suit More...

Job Description: The main skills we are looking for Experience in System Engineer EWIS – CS25 H Experience in Wiring Diagram Experience in Cable Harness Very important to create the documents with requirements as per EASA Standards

In the Clinical Trial Execution Service department your role will support the Clinical Trial Lab Management in the operational daily business.Create and maintain trial related lab trackers (e.g. on screening samples lab reconciliation tracker sample destruction etc.) as required More...

Within our department Molecular Technologies & Stem Cell Therapy you will support projects in the field of hematopoietic stem cell (HSC) therapy.You will assist in the development of innovative products and the automation of GMPcompliant processes using the CliniMACS Prodigy platf More...

As the head of Sales Enablement you will be responsible for managing the design development and deployment of the sales process sales training product education sales skills enablement programs sales bootcamps sales academy and sales certification programs that drive elite sales perfo More...

In the Clinical Trial Execution Service department your role will support our trial processes and activities in line with our gotomarket strategy for Investigational Medicinal Products (IMPs) especially in hematological and oncological indications. As a key contact for bioanalytical s More...

The Senior Recruiter is responsible for Service Excellence throughout the recruitment cycle. The Senior Recruiter acts as a brand ambassador for their client and partners with the hiring managers in a consultative capacity. They are focused on delivering top talent for their hiring ma More...

As an SAP specialist (m/f/d) in the process industry segment you will manage customer projects with a focus on the area of PPPI.You will support all project phases from conception design customizing and POC to the rollout of SAP ECC and S/4HANA.You actively work on the further develo More...