Skip to content

This website works best using cookies which are currently disabled.Cookie policy  Allow cookies
JobServe
 

Job Application

 
 
 

Please answer the following questions in order to begin the process of your application.

 
 
Email Address *
 
 
 
File Attachments:
(2MB file maximum. doc, docx, pdf, rtf or txt files only)
 
Attach a CV * 
 
 
 * denotes required field
 
 
 

Key Privacy Information

When you apply for a job, JobServe will collect the information you provide in the application and disclose it to the advertiser of the job.

If the advertiser wishes to contact you they have agreed to use your information following data protection law.

JobServe will keep a copy of the application for 90 days.

More information about our Privacy Policy.

 

Job Details

 

Quality Engineering Specialist (Contract)

Location: Aargau Country: Switzerland
 
Join a Leading Biopharma Company as a Quality Engineering Specialist!

On behalf of our client, a multinational company in the pharmaceutical, biotechnology, and nutrition sectors, we are looking for QA Specialist (CSV & Automation) responsible for the qualification and validation compliance of equipment and computerized systems related to aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products as part of CAPEX project portfolio in Stein, AG.

Contract Type: Contract
Start Date: ASAP
Location: Stein
Workload: 100%
Duration: 1 year

Your mission:
Responsible for the compliance of commissioning and qualification of large CAPEX projects (eg new drug product facility) from ideation to execution phases, throughout all design phases:
Ensure that qualification/validation plan and execution of equipment, infrastructure and computerized systems are in place by adhering to the company's Quality policies
Approve SOPs, commissioning/qualification/validation protocols and reports as well as project related CQV/CSV documents (eg URS, FAT/SAT, etc.)
Provide QA leadership, oversight and support to staff on qualification/validation topics related to ongoing projects and ensures that selected vendors are qualified
Act as first point of contact within GQE for any area related to the life cycle and compliance for equipment, infrastructure and computerized-systems qualification/validation, including documentation in shared global systems (eg Kneat, Trackwise, DMS, Unifier, etc.)
Manage Quality deviations, changes and CAPAs/tasks in an open and timely manner, taking leadership for their resolution, but escalating when necessary

Your background:
Bachelor or Master's degree in Engineering, Life Sciences or related field
Significant experience in the GMP regulated pharmaceutical industry, preferably in a role within a Quality Unit
Experience in a QA role for the CSV/Automation of GMP systems related to aseptic fill-finish processes and facility (filling equipment, lyophilization, clean utilities, and clean room facilities)
Fluent in English, German would be an advantage

What's on Offer?
An opportunity to prove your expertise in a leading global company.
Be part of a dynamic team and a positive company culture.

If this sounds like you, don't hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: (see below)

By applying for this position, I consent to the Swisslinx Group of companies:
- storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external Servers for the purpose of informing me of potential employment opportunities
- using my personal information or
- supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities
- transferring where applicable my personal information to a country outside the EEA/EFTA

I also hereby agree to the Swisslinx privacy policy and Terms of Use


Posted Date: 28 Oct 2024 Reference: JS16341 Employment Business: Swisslinx Contact: