Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

Pharmaceutical Verification Manager (m/f/d) Full-time at AKTIV Personal-Service GmbH

Berlin, Berlin, Germany -

Full Time

Start Date

Immediate

Expiry Date

04 Jan, 27

Salary

90000.0

Posted On

06 Oct, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Industry

Pharmaceutical Manufacturing

Description

Your responsibilities as a Scientist/Device Engineer (m/f/d) in the pharmaceutical industry:

Planning and execution of design verifications
Product approvals and technical documentation
Evaluation of regulatory changes and their implementation in development processes
Participation in interdisciplinary development teams
Creation of verification plans, execution of studies and documentation of the results

Your profile as a Scientist/Device Engineer (m/f/d) Pharma:

Completed Bachelor's or Master's degree in a life science discipline, such as medical technology, biotechnology, pharmacy, chemistry, biology, molecular biology, cell biology, or engineering with a focus on biomedicine.
Experience in a regulated environment, especially with design control processes for combination products
Knowledge of planning, conducting, and documenting design verifications

How To Apply:

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

Responsibilities

Your responsibilities as a Scientist/Device Engineer (m/f/d) in the pharmaceutical industry:

Planning and execution of design verifications
Product approvals and technical documentation
Evaluation of regulatory changes and their implementation in development processes
Participation in interdisciplinary development teams
Creation of verification plans, execution of studies and documentation of the results

Your profile as a Scientist/Device Engineer (m/f/d) Pharma:

Completed Bachelor's or Master's degree in a life science discipline, such as medical technology, biotechnology, pharmacy, chemistry, biology, molecular biology, cell biology, or engineering with a focus on biomedicine.
Experience in a regulated environment, especially with design control processes for combination products
Knowledge of planning, conducting, and documenting design verifications