Batch Record Reviewer
Infos sur l'emploi
- Date de publication :13 janvier 2025
- Taux d'activité :100%
- Type de contrat :Durée indéterminée
- Langue :anglais (Courant)
- Lieu de travail :Visp / Upper Valais
On behalf of our client, we are seeking a detail-oriented and proactive Batch Record Review and Support Specialist to join their team in Visp.
This role is critical in ensuring the accuracy and compliance of executed batch records within a GMP-regulated environment, supporting smooth operations and timely product releases.
Location: Visp, Switzerland
Contract Type: Contract
Duration: Until 14/07/2025
Start Date: ASAP
Workload: 100%
Your Responsibilities:
* Review executed electronic Batch Records, including cleaning logs, production documentation, temperature reports, test procedures (HEPT, FIT), equipment protocols (autoclave,
washing machines), calibration records, sample results (LIMS), and logbooks.
* Evaluate and clarify review comments with the operations team and liaise with the responsible QA Manager.
* Initiate and support the resolution of deviations and investigations related to batch record observations.
* Assist in initiating Change Requests (CRs) and Temporary Change Requests (TCRs).
* Prepare documentation packages to facilitate timely QA release.
Your Background:
* Prior experience in GDP and GMP-regulated pharmaceutical/API industries is a strong advantage.
* Proven ability to identify non-compliance and quality standard gaps.
* Excellent communication skills and ability to collaborate effectively across interfaces within the organization; strong team player.
* Structured, organized, and focused approach to work with a solution-oriented mindset.
* Agile, motivated, and dynamic with the ability to deliver reliable results under pressure.
* Familiarity with MES Syncade and DeltaV systems is preferred.
* Fluent in English; basic knowledge of German is an advantage.
What's on Offer:
* An opportunity to contribute to the quality and compliance of a leading pharmaceutical organization.
* A collaborative and dynamic work environment in Visp, Switzerland.
* A chance to develop professionally in a fast-paced, innovative setting.
If you are passionate about ensuring quality standards and compliance in the pharmaceutical industry and meet the above requirements, we look forward to receiving your application!
For more information, please contact:
Veronika von Mentzer, Recruiter
Email: Write an email
This role is critical in ensuring the accuracy and compliance of executed batch records within a GMP-regulated environment, supporting smooth operations and timely product releases.
Location: Visp, Switzerland
Contract Type: Contract
Duration: Until 14/07/2025
Start Date: ASAP
Workload: 100%
Your Responsibilities:
* Review executed electronic Batch Records, including cleaning logs, production documentation, temperature reports, test procedures (HEPT, FIT), equipment protocols (autoclave,
washing machines), calibration records, sample results (LIMS), and logbooks.
* Evaluate and clarify review comments with the operations team and liaise with the responsible QA Manager.
* Initiate and support the resolution of deviations and investigations related to batch record observations.
* Assist in initiating Change Requests (CRs) and Temporary Change Requests (TCRs).
* Prepare documentation packages to facilitate timely QA release.
Your Background:
* Prior experience in GDP and GMP-regulated pharmaceutical/API industries is a strong advantage.
* Proven ability to identify non-compliance and quality standard gaps.
* Excellent communication skills and ability to collaborate effectively across interfaces within the organization; strong team player.
* Structured, organized, and focused approach to work with a solution-oriented mindset.
* Agile, motivated, and dynamic with the ability to deliver reliable results under pressure.
* Familiarity with MES Syncade and DeltaV systems is preferred.
* Fluent in English; basic knowledge of German is an advantage.
What's on Offer:
* An opportunity to contribute to the quality and compliance of a leading pharmaceutical organization.
* A collaborative and dynamic work environment in Visp, Switzerland.
* A chance to develop professionally in a fast-paced, innovative setting.
If you are passionate about ensuring quality standards and compliance in the pharmaceutical industry and meet the above requirements, we look forward to receiving your application!
For more information, please contact:
Veronika von Mentzer, Recruiter
Email: Write an email
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