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QA Batch Record Reviewer 100%
vor 2 Wochen
Visp, Schweiz Careforce VollzeitKey Responsibilities Review executed batch records including production documentation and raw data Ensure full and accurate documentation to support batch release Clarify record comments with operational teams and assess with the responsible QA Manager Support the initiation of deviations and investigations related to record-review findings Job ID 18408
Batch Record Reviewer
vor 2 Wochen
Contract duration: 1 year
Location: Visp
The main task is to check the control of completed production batch records, data is transferred to control systems and participate in review meetings in close cooperation with QA and operations.
Depending on the workload, support is also required for general work in the company, such as creating presentations, ordering office supplies, archiving documents, etc.
As an in-house batch record reviewer, you are responsible for the independent and timely execution of the production document control according to in-house instructions. You will support the investment team by providing and preparing as well as maintaining production-relevant documents. Overall, they also support other company groups in the maintenance and provision of documents and create added value for the company.
Responsibilities:
- The timely and independent execution of the operational batch record review (manufacturing protocols, cleaning protocols, etc.) in accordance with the company's internal work instructions
- Maintenance of company document lists (KPIs, expense lists, etc.) with the support of the investment team and operations.
- General document support on behalf of the project teams (e.g. provision and collection of documents, inspection of labels and the like)
- Creation of the production certificate after the batch is completed.
- Care and responsibility for the controlled copied work instructions in the company.
- Responsibility for the archiving of process-relevant documents from the company
Requirements:
- Experience in a pharmaceutical environment in a similar role
- Very good written and spoken German and English
- Understanding the applicable cGMP regulations
- Good IT skills, especially in MS Office
