Quality Control Scientist in Neuchâtel

The job holder is accountable for life cycle management activities of analytical assays performed in the QC.
Laboratories of Neuchâtel – Switzerland with a focus on:

Laboratory Investigations
Critical Material Qualification
Laboratory Method Transfers

In addition, the job holder also supports daily QC activities following cGMP, and EHS requirements.

Daily activities:

Validation and Qualification Activities

Author transfer protocols and reports for assays
Author qualification plans and reports for critical reagents
Oversee validation and qualification activities executed by analysts, provide training and support
Execute and documents experiments

Investigation Leads

Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change
Conduct/participate in risk assessments, root cause analysis and investigations
Own Laboratory Investigations and CAPA

Quality Control Support Activities

Support the application of industry specific compliance standards/regulations to
assays life cycle management activities
Participate to daily activities upon request (provide technical and statistical support)

Your profile:

University or engineering degree in analytical chemistry, biotechnology, biochemistry
1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment
Experience in GMP Laboratory activities
Good knowledge of method transfer
Good knowledge of critical reagent qualification
Experience in problem solving and deviation management
Good Knowledge of statistical tools
Fluent in French and English (C1 written and spoken)
Proficiency in all aspects of standard IT tools
Excellent collaboration skills and teamwork mindset
Good trouble shooting and problem-solving skills
Ability to work independently in a fast-paced environment
Ability to manage multiple priorities and know when to escalate issues for resolution
Effective communicator
Demonstrated ability to synthesize information
Demonstrated ability to give and receive feedback

For our client, an international company in Neuchâtel, we are looking for a
QC Associate Scientist.

Start date:ASAP
Contract: for 6 months via Randstad
Extension: possible
Workplace: Neuchâtel
Workload: 100%

Responsibilities:

The job holder is accountable for life cycle management activities of analytical assays performed in the QC.
Laboratories of Neuchâtel – Switzerland with a focus on:

Laboratory Investigations
Critical Material Qualification
Laboratory Method Transfers

In addition, the job holder also supports daily QC activities following cGMP, and EHS requirements.

Daily activities:

Validation and Qualification Activities

Author transfer protocols and reports for assays
Author qualification plans and reports for critical reagents
Oversee validation and qualification activities executed by analysts, provide training and support
Execute and documents experiments

Investigation Leads

Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change
Conduct/participate in risk assessments, root cause analysis and investigations
Own Laboratory Investigations and CAPA

Quality Control Support Activities

Support the application of industry specific compliance standards/regulations to
assays life cycle management activities
Participate to daily activities upon request (provide technical and statistical support)

Your profile:

University or engineering degree in analytical chemistry, biotechnology, biochemistry
1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment
Experience in GMP Laboratory activities
Good knowledge of method transfer
Good knowledge of critical reagent qualification
Experience in problem solving and deviation management
Good Knowledge of statistical tools
Fluent in French and English (C1 written and spoken)
Proficiency in all aspects of standard IT tools
Excellent collaboration skills and teamwork mindset
Good trouble shooting and problem-solving skills
Ability to work independently in a fast-paced environment
Ability to manage multiple priorities and know when to escalate issues for resolution
Effective communicator
Demonstrated ability to synthesize information
Demonstrated ability to give and receive feedback

kontaktiere uns.

wir sind da um deine Fragen zu beantworten.

LS

Luciana Sardo

+41 58 201 55 55
Basel Professionals IT & Life Sciences

der Bewerbungsprozess.

Erfahre wie der Bewerbungsprozess aussieht. Finde heraus wie wir dir helfen werden, diesen Job zu bekommen.

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mit randstad bewerben.

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Wir werden dich kontaktieren.

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deine registrierung.

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background check.

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der perfekte job für dich.

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das interview.

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dein start im neuen job.

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beginne deinen neuen job.

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.

,
veröffentlicht vor 4 Tagen
läuft am 30. November 2024 ab

Job Details

zusammenfassung.

Neuenburg, Neuchâtel

Kontakt

Luciana Sardo

Referenznummer

20031

Beschleunige die Bewerbung, indem du dein Profil teilst

Job Details

For our client, an international company in Neuchâtel, we are looking for a
QC Associate Scientist.

Start date:ASAP
Contract: for 6 months via Randstad
Extension: possible
Workplace: Neuchâtel
Workload: 100%

Responsibilities:

Firma: Randstad Schweiz AG

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