Expert (m/w/d) QRM & Digital Documentation F1 at Pfizer Canada

berlin, Berlin, Germany -

Full Time

Start Date

Immediate

Expiry Date

21 Dec, 26

Salary

90000.0

Posted On

22 Sep, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Industry

Pharmaceutical Manufacturing

Description

Here's what you can expect:

Creation and updating of risk analyses
Creation and updating of SOPs
Review and incorporation of requirements from higher-level guidelines
Initiation and monitoring of change control
Participation in strategic projects in the manufacturing sector
Monitoring and ensuring quality standards with regard to change control management
Design of specifications and initiation of optimizations regarding process capability
Evaluation of processes with regard to digitization and automation potential
Creation, editing, testing and maintenance of digital documents
Supporting the Business Process Owner and Head of Manufacturing in the creation, review and testing of AMPS workflows (EBR / MBR) and adaptation and optimization of accompanying CD/SOP documents.

You bring the following with you:

A completed vocational training as a pharmaceutical technician (m/f/d) with at least 3 years of professional experience
Ideally, professional experience in the manufacture and testing of pharmaceuticals.
Experience with common IT systems
Very good German and good English skills
Awareness of quality, efficiency and effectiveness

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

Here's what you can expect:

Creation and updating of risk analyses
Creation and updating of SOPs
Review and incorporation of requirements from higher-level guidelines
Initiation and monitoring of change control
Participation in strategic projects in the manufacturing sector
Monitoring and ensuring quality standards with regard to change control management
Design of specifications and initiation of optimizations regarding process capability
Evaluation of processes with regard to digitization and automation potential
Creation, editing, testing and maintenance of digital documents
Supporting the Business Process Owner and Head of Manufacturing in the creation, review and testing of AMPS workflows (EBR / MBR) and adaptation and optimization of accompanying CD/SOP documents.

You bring the following with you:

A completed vocational training as a pharmaceutical technician (m/f/d) with at least 3 years of professional experience
Ideally, professional experience in the manufacture and testing of pharmaceuticals.
Experience with common IT systems
Very good German and good English skills
Awareness of quality, efficiency and effectiveness