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Company DescriptionJob DescriptionThe QC Microbiology Sr. Manager will be responsible for managing the microbiology testing capabilities for a large scale manufacturing site in Solothurn,...
5 hours ago - Source Neuvoo PREMIUM Europe
JobdescriptionAre you an IT Project Manager and you have experience in the Pharmaceutical or Biotech Environment? Our client is looking for an experienced candidate willing to take up this...
5 hours ago - Source Neuvoo PREMIUM Europe
Company DescriptionJob DescriptionAs Quality Control Associate, you will be responsible for Raw Material Release within the Quality department, which includes:Ensure raw material testing based on...
5 hours ago - Source Neuvoo PREMIUM Europe
Company DescriptionJob DescriptionLogistic Management: Work cross functionally to support purchasing, receipt, storage and distribution of test solutions and laboratory reagents for the Solothurn...
5 hours ago - Source Neuvoo PREMIUM Europe
Company DescriptionJob DescriptionReviewing validation documentation and additional protocols and reportsReviewing GMP documents and raw data for compliance to applicable regulatory and corporate...
5 hours ago - Source Neuvoo PREMIUM Europe
JobdescriptionOur client, biotechnology company in Solothurn area is looking for aProject ManagerContract until 30.06.2021Start: asapJOB OVERVIEW:The Project Manager is an intermediate level resource...
5 hours ago - Source Neuvoo PREMIUM Europe
Company DescriptionJob Description1. Quality Operation oversightDesigns and manages (including their development) the Solothurn Operation Quality Team of subject matter experts who...
5 hours ago - Source Neuvoo PREMIUM Europe
The incumbent supervises Manufacturing Associates, schedules shift tasks, ensures cGMP compliance and safety procedures are adhered to. He/She ensures manufacturing documentation is updated and...
1 day ago - Source Jobleads Europe
Full-time Region: EU+/Canada Job Description JOB PURPOSE: Industrial Engineers take on an integral role at Biogen by driving and implementing continuous improvement throughout the business. The...
1 day ago - Source Jobleads Europe
This person is responsible for coordinating manufacturing activities across 1 BMC, 5 shifts and support departments. Cross-shift and cross-functional communications will be a daily focus of this...
1 day ago - Source Jobleads Europe
Are you anIT Project Managerand you have experience in thePharmaceuticalorBiotechEnvironment? Our client is looking for an experienced candidate willing to take up this challenge: Lead moderate to...
1 day ago - Source Jobleads Europe
Job Description JOB PURPOSE: Industrial Engineers take on an integral role at Biogen by driving and implementing continuous improvement throughout the business. The Operations and Systems Improvement...
5 hours ago - Source Neuvoo BULK Europe
Job Description Contribute to the development and management of the Annual Affiliate Audit Schedule (5%) Schedule, prepare, conduct and report Affiliate audit and compliance monitoring activities to...
5 hours ago - Source Neuvoo BULK Europe
Job Description JOB PURPOSE: The incumbent understands industry-wide and Regulatory expectations for validation, and works with other members of management to ensure validation practices are...
5 hours ago - Source Neuvoo BULK Europe
Job Description Reviewing validation documentation and additional protocols and reports Reviewing GMP documents and raw data for compliance to applicable regulatory and corporate guidance documents,...
5 hours ago - Source Neuvoo BULK Europe
Job Description JOB PURPOSE: The Lean Manufacturing specialist role follows the Lean manufacturing principles. The role directly supports all departments at the Solothurn Manufacturing Site. Main...
5 hours ago - Source Neuvoo BULK Europe
The purpose of the Head of Validation Engineering position is to manage the Validation Engineering group within the Engineering Department to maintain highly reliable and compliant process equipment...
1 day ago - Source Jobleads Europe
Job DescriptionDevelops the site manufacturing schedule for day to day operations and supports planning activities for long term timelines. Responsible for tactical day-to-day scheduling and...
5 hours ago - Source Neuvoo BULK Europe
Job Description As Quality Control Associate, you will be responsible for Raw Material Release within the Quality department, which includes: Ensure raw material testing based on rapid spectroscopic...
5 hours ago - Source Neuvoo BULK Europe
Job DescriptionThis Engineer is responsible for the operation, maintenance and expansion of the manufacturing data systems for Biogen’s Next Generation Manufacturing Execution System supporting...
5 hours ago - Source Neuvoo BULK Europe
Company DescriptionJob DescriptionPrepare data extract reports for validation protocol and review of the protocols accordingly. Main point of contact for Eurofins PSS to coordinates daily activities...
5 hours ago - Source Neuvoo PREMIUM Europe
The incumbent supervises Manufacturing Associates, schedules shift tasks, ensures cGMP compliance and safety procedures are adhered to. He/She ensures manufacturing documentation is updated and...
1 day ago - Source Jobleads Europe
Job Description JOB PURPOSE: This person is responsible for coordinating manufacturing activities across 1 BMC, 5 shifts and support departments. Cross-shift and cross-functional communications will...
5 hours ago - Source Neuvoo BULK Europe
Job Description This Engineer is responsible for the operation, maintenance and expansion of the manufacturing data systems for Biogen’s Next Generation Manufacturing Execution System supporting...
5 hours ago - Source Neuvoo BULK Europe
Job Description JOB PURPOSE: The purpose of the Head of Validation Engineering position is to manage the Validation Engineering group within the Engineering Department to maintain highly reliable and...
5 hours ago - Source Neuvoo BULK Europe
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