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Clinical Packaging Supervisor

Job Field:
Clinical Research Jobs, Testing & Analysis Jobs
Discipline:
Laboratory Technician Jobs
Country:
Switzerland
Region:
Switzerland All
Contract Type:
Permanent
Currency:
Unspecified
Salary Description:
Competitive
Posted:
04-Sep-17
Recruiter:
Clintec
Job Ref:
SWI CPS 080817 AD

Clinical Packaging Supervisor (GMP) - Permanent, Greater Lucerne Area

Clintec, Global CRO, is currently looking to hire an experienced Clinical Packaging Supervisor to work dedicated to our top 5 pharmaceutical client, based from their state of the art facility near Lucerne, Switzerland. Apply now to become part of our global team!

Role Overview

We are looking for a Packaging Supervisor, supporting our clients GCS (Global Clinical Supply) Clinical Packaging Group. The role includes general support of the GCS Clinical Packaging group and interfacing with other GSC groups in both the US and the UK, as well with other Departments at our client's Swiss site. This position will support the Clinical Packaging & Distribution Lead.

Responsibilities:

Supports the Clinical Packaging & Distribution Lead
Compliance
Quality checks for packaging batch records
Pre- and post-Execution review including In-Process-Controls
Drives speed, flexibility and reliability
Achieving of batch records
Checks SAP transactions and closes work orders
Provides support to updates and review of Standard Operation Procedures and other GMP relevant documents
Serves as a point of contact for issue resolution
Supports investigations and changes
Supports equipment qualifications
Supports walkthrough Audits and Internal Audits
Tracks and monitors local operational and quality performance.
Escalates issues to the Clinical Packaging & Distribution Lead as appropriate
Assists in development and delivery of metrics

Qualifications and Experience Required:

Min. 3 years’ experience in Quality, Technical Operations, related Business Operations or GMP regulated environment
Demonstrated Quality or Manufacturing/Packaging experience in the areas of pharmaceutical and / or biologics manufacturing or packaging
Demonstrated problem-solving skills
Knowledge of cGMPs, data management, collection, and analysis
Possesses excellent interpersonal, inclusion, and communication skills
Appreciates and respects diversity, cultures, and norms in a team
Drives results
Escalation of issues / concerns to management, as appropriate
Fluent in both German and English
Available to work site based 20 minutes west of Lucerne
Click apply or send your CV to Adam Davis, Senior Global Resourcing Executive - adavis@clintec.com

Company Information:

Clintec AG in Zug is a global CRO present in over 50 countries worldwide. We are currently working on strategic assignments as a pharmaceutical service provider with several major multinational pharmaceutical companies in Switzerland. As part of our expansion to our established team in Switzerland, we have a number of exciting opportunities available.

By working for Clintec you will have exposure to interesting assignments with leading players in global pharma R&D, and hence you can further your career in a dynamic, stable environment where you can be assured of rewarding benefits.

Closing Date:
02/10/2017

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