QC Analyst II – Quality Team Leader QC, no-188

Location
CH-Stein
Start
01.02.2023
End
31.07.2024
Workload
100 %
All-in / Hour
see job description
Total Hours
3128

Deadline:

Deadline
21.11.2022

 

QC Analyst II – Quality Team Leader QC, no-188

Location
CH-Stein
Workload
100 %

Start

01.02.2023

End

31.07.2024

DEADLINE

Deadline
21.11.2022

  • CH-Stein
  • CH-Stein01.02.202331.07.2024100 % 3128see job descriptionDeadline
    21.11.2022

For our customer located in Stein, Switzerland we are currently looking for a: QC Analyst II – Quality Team Leader QC (m/f/x)

  • Location: CH-Stein (100% on-site / no home-office)
  • Duration: 01.02.2023 – 31.07.2024
  • Pay rate: 35,86 – 40,34 chf/h

Tasks & Responsibilities

Operational

  • Sample storage and management
  • Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
  • Ensure all activities in compliance with cGxP, incl. data integrity

HSE

  • Comply with all HSE guidelines
  • Detect and report potential accident, risks and propose solutions
  • Responsible for participating in initial training and retraining

Key Performance Indicators 

  • Orders are processed correctly and quickly
  • no waiting times due to wrong or delayed order
  • Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time
  • Ensure constant readiness for inspection, no critical complaints from superiors and inspectors
  • Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities
  • Finding and implementing optimization options to reduce costs
  • Completed training plan.
    Dimensions of the Job 
  • Impact on the organization Direct impact on Quality, compliance, and product timely delivery

Must Haves

Specific major accountabilities
In addition to the defined accountabilities of Job Profile the following accountably are relevant:

  • Perform and document lab analysis (standard and more complex techniques)
  • Support analytical investigations and OOx
  • Implementation of innovative DP/DS methods from development
  • Participation in co-validation activities or analytical transfers
  • Reports to (solid line): QC Lead Microbiology or Quality Team Leader QC Microbiology (depending on size)

Relevant Experience

  • Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique; microbiological analysis.

Education & Qualification

  • Completed apprenticeship as a laboratory assistant or equivalent training

Languages

  • Basic (oral and written) in English;
  • fluent in local language – German (oral and written)

Competencies

  • Collaboration; result-oriented
  • Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
  • Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
  • Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making
  •  

 

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Stein
  • CH-Stein01.02.202331.07.2024100 % 3128see job descriptionDeadline
    21.11.2022

For our customer located in Stein, Switzerland we are currently looking for a: QC Analyst II – Quality Team Leader QC (m/f/x)

  • Location: CH-Stein (100% on-site / no home-office)
  • Duration: 01.02.2023 – 31.07.2024
  • Pay rate: 35,86 – 40,34 chf/h

Tasks & Responsibilities

Operational

  • Sample storage and management
  • Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
  • Ensure all activities in compliance with cGxP, incl. data integrity

HSE

  • Comply with all HSE guidelines
  • Detect and report potential accident, risks and propose solutions
  • Responsible for participating in initial training and retraining

Key Performance Indicators 

  • Orders are processed correctly and quickly
  • no waiting times due to wrong or delayed order
  • Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time
  • Ensure constant readiness for inspection, no critical complaints from superiors and inspectors
  • Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities
  • Finding and implementing optimization options to reduce costs
  • Completed training plan.
    Dimensions of the Job 
  • Impact on the organization Direct impact on Quality, compliance, and product timely delivery

Must Haves

Specific major accountabilities
In addition to the defined accountabilities of Job Profile the following accountably are relevant:

  • Perform and document lab analysis (standard and more complex techniques)
  • Support analytical investigations and OOx
  • Implementation of innovative DP/DS methods from development
  • Participation in co-validation activities or analytical transfers
  • Reports to (solid line): QC Lead Microbiology or Quality Team Leader QC Microbiology (depending on size)

Relevant Experience

  • Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique; microbiological analysis.

Education & Qualification

  • Completed apprenticeship as a laboratory assistant or equivalent training

Languages

  • Basic (oral and written) in English;
  • fluent in local language – German (oral and written)

Competencies

  • Collaboration; result-oriented
  • Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
  • Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
  • Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making
  •  

 

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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