Manufacturing Technician [Role in SHIFT] / ta-612

Location
CH-Neuchatel
Start
01.07.2024
End
30.06.2025
Workload
100 %
All-in / Hour
rate negotiable
Total Hours

Deadline:

 

Manufacturing Technician [Role in SHIFT] / ta-612

Location
CH-Neuchatel
Workload
100 %

Start

01.07.2024

End

30.06.2025

DEADLINE

  • CH-Neuchatel
  • CH-Neuchatel01.07.202430.06.2025100 % rate negotiable

For our customer located in Neuchatel/Switzerland we are currently looking for a: Manufacturing Technician [Role in SCHIFT] (m/f/x)

 

  • Location: 100 % Neuchatel
  • Role in SCHIFT 2x2x2x4 (2 mornings, 2 afternoons, 2 nights and 4 consecutive days off) 
  • Branch: Pharma
  • Duration: 01.07.2024 – 30.06.2025
  • French speaker needed!

Tasks & Responsibilities

The main objective of the production technician is to carry out activities related to the of an active pharmaceutical substance.
Must be able to:

  • comply with cGMP, BDP and EHS standards
  • Carry out routine and non-routine process activities (schedule completion)
  • Report technical and/or organizational problems
  • Share knowledge with colleagues
  • Propose ideas for continuous improvement
  • Maintain the condition of production areas

RESPONSIBILITIES:

  • Responsible for compliance with cGMP, BDP and EHS standards
  • Responsible for training follow-up
  • Responsible for proper execution of work
  • Responsible for reporting any problems encountered
  • Be 100% autonomous in the activities of his/her work area
  • Involved in continuous improvement
  • Respect and apply leadership behaviors
  • Respect for organizational processes
  • Verification 

Must Haves

  • BAC + 2 (majoring in biotechnology, chemistry, biology, biochemistry) or equivalent
  • Good knowledge of one of the following processes: cell culture and/or protein purification process support activities on a production line
  • Ideally CFC in chemical and pharmaceutical production or equivalent
  • Ideally, a first successful experience in the pharmaceutical, food or chemical industry.
  • Knowledge of Good Manufacturing Practices (cGMP)
  • Knowledge of the controlled atmosphere working environment
  • Knowledge of pack office software (Outlook, Excel, Word, PWP)
  • Good verbal and written communication skills in French (minimum level B2).

Nice to Haves

  • Good verbal and written communication
  • Methodical and rigorous approach to work
  • Availability and flexibility
  • Organizational skills
  • Dynamic and willing character
  • Team spirit
  • Ownership

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-Neuchatel
  • CH-Neuchatel01.07.202430.06.2025100 % rate negotiable

For our customer located in Neuchatel/Switzerland we are currently looking for a: Manufacturing Technician [Role in SCHIFT] (m/f/x)

 

  • Location: 100 % Neuchatel
  • Role in SCHIFT 2x2x2x4 (2 mornings, 2 afternoons, 2 nights and 4 consecutive days off) 
  • Branch: Pharma
  • Duration: 01.07.2024 – 30.06.2025
  • French speaker needed!

Tasks & Responsibilities

The main objective of the production technician is to carry out activities related to the of an active pharmaceutical substance.
Must be able to:

  • comply with cGMP, BDP and EHS standards
  • Carry out routine and non-routine process activities (schedule completion)
  • Report technical and/or organizational problems
  • Share knowledge with colleagues
  • Propose ideas for continuous improvement
  • Maintain the condition of production areas

RESPONSIBILITIES:

  • Responsible for compliance with cGMP, BDP and EHS standards
  • Responsible for training follow-up
  • Responsible for proper execution of work
  • Responsible for reporting any problems encountered
  • Be 100% autonomous in the activities of his/her work area
  • Involved in continuous improvement
  • Respect and apply leadership behaviors
  • Respect for organizational processes
  • Verification 

Must Haves

  • BAC + 2 (majoring in biotechnology, chemistry, biology, biochemistry) or equivalent
  • Good knowledge of one of the following processes: cell culture and/or protein purification process support activities on a production line
  • Ideally CFC in chemical and pharmaceutical production or equivalent
  • Ideally, a first successful experience in the pharmaceutical, food or chemical industry.
  • Knowledge of Good Manufacturing Practices (cGMP)
  • Knowledge of the controlled atmosphere working environment
  • Knowledge of pack office software (Outlook, Excel, Word, PWP)
  • Good verbal and written communication skills in French (minimum level B2).

Nice to Haves

  • Good verbal and written communication
  • Methodical and rigorous approach to work
  • Availability and flexibility
  • Organizational skills
  • Dynamic and willing character
  • Team spirit
  • Ownership

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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