Manufacturing Operations Specialist

Job DescriptionAbout the Role:We are seeking a skilled Manufacturing Associate II to join our team. As a key member of our manufacturing department, you will be responsible for performing and documenting daily manufacturing operations in a cGMP environment.Key Responsibilities:

Job Description:As a Manufacturing Associate II, you will be responsible for performing daily manufacturing operations in a cGMP environment. This includes the operation of process equipment, execution of validation protocols, and revising cGMP documents to ensure compliance. You will also be responsible for maintaining equipment and facilities, and...

Manufacturing Operations Role:This position is responsible for executing manufacturing processing steps and/or manufacturing support activities in a cGMP environment. The successful candidate will have a solid understanding of Biotech processes and be able to follow and comply with written procedures and protocols. They will also have strong documentation...

Job Overview    We are seeking an experienced Manufacturing Associate II to join our team. In this role, you will be responsible for performing daily manufacturing operations in a cGMP environment. This includes operating process equipment, executing validation protocols, and revising cGMP documents to ensure compliance.    Key Responsibilities•...

We are a global team at Biogen, committed to delivering life-changing medicines. As an Operator II Utilities, you will play a vital role in ensuring the smooth operation of our industrial systems. Your responsibilities will include:">Operating and Inspecting Industrial Systems:">You will be responsible for operating, inspecting, and maintaining Black...

The coordinator V is responsible for supporting / enabling manufacturing activities in regard to Compliance, Documentation, Recipe driven operations, Changeover, Tech transfer, and or Training for day-to-day activity. In addition, the Coordinator V is in charge to represent Manufacturing by participating in intra, cross site alignments and cross functional...

Jobdescription For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II. General Information: Start date: 01.02.2025 End date: 31.01.2026 Extension: Possible Workplace: Solothurn Workload: 100% Remote/Home office: Not available Job Summary: Performs and documents daily manufacturing operations in a cGMP...

Jobdescription For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.General Information:Start date: 01.02.2025End date: 31.01.2026Extension: Possible Workplace: Solothurn Workload: 100% Remote/Home office: Not available Job Summary: Performs and documents daily manufacturing operations in a cGMP environment...

**Job Description** About This Role** As a Senior Manufacturing Associate III, your primary role involves Perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and...

JobdescriptionFor our client, an international company in Solothurn, we are looking for a Manufacturing Associate II. General Information: Start date: 01.02.2025 End date: 31.01.2026 Extension: PossibleWorkplace: SolothurnWorkload: 100%Remote/Home office: Not availableJob Summary:Performs and documents daily manufacturing operations in a cGMP environment...

Job DescriptionAbout This RoleIn this role, you will be responsible for leading a team of Manufacturing Associates, overseeing daily shift tasks, and ensuring compliance with cGMP standards and safety procedures. You will play a key role in maintaining and revising manufacturing documentation to ensure accuracy and compliance with industry regulations.As a...

As a Manufacturing Upstream Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If you thrive in a...

For our client, an international company in Solothurn, we are looking for a Manufacturing Associate II.General Information:Start date: 01.02.2025End date: 31.01.2026Extension: PossibleWorkplace: SolothurnWorkload: 100%Remote/Home office: Not availableJob Summary:Performs and documents daily manufacturing operations in a cGMP environment including operation...

**Company Description** About This Role** As a Manufacturing associate V you'll perform and document daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing...

About This Role As a Manufacturing Associate IV, you'll perform processing steps and manufacturing support activities in our facilities in Luterbach (Solothurn). You will be the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. Your responsibilities include performing and...

About This Role In this role, you will lead and oversee a team of Manufacturing Associates, coordinate shift tasks, and ensure a commitment to cGMP compliance and safety procedures. You will play a pivotal role in maintaining updated manufacturing documentation and serve as a system expert, leading technical issue resolution and troubleshooting while...

In this role, you will lead and oversee a team of Manufacturing Associates, coordinate shift tasks, and ensure a commitment to cGMP compliance and safety procedures. You will play a pivotal role in maintaining updated manufacturing documentation and serve as a system expert, leading technical issue resolution and troubleshooting while actively representing...

Job DescriptionAs a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If...

Job Description As a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP...

As a Manufacturing Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream or downstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards. If you thrive in...

Job Description As a Manufacturing Upstream Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial role in the daily upstream manufacturing activities within a cGMP environment. Your responsibilities include operating process equipment, executing validation protocols, and ensuring strict compliance with cGMP standards....

Social network you want to login/join with:Manufacturing Upstream Associate III, LuterbachClient:BiogenLocation:Job Category:ManufacturingJob Reference:5c0ac7491a67Job Views:8Posted:21.01.2025Expiry Date:07.03.2025Job Description:Job DescriptionAs a Manufacturing Upstream Associate III, you'll be at the heart of our cutting-edge operations, playing a crucial...

Social network you want to login/join with:Associate II, Integrated Downstream Quality Operations, LuterbachClient:BiogenLocation:Job Category:OtherJob Reference:9934de2eb6f1Job Views:9Posted:21.01.2025Expiry Date:07.03.2025Job Description:About This RoleThe Associate II within the Integrated Downstream Quality Operations team is part of the Quality...

About This Role The Associate II within the Integrated Downstream Quality Operations team is part of the Quality Department at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/She focuses on Quality Operations and Quality Engineering activities for downstream manufacturing and equipment. The Solothurn site is...

**Maintenance Technician Manufacturing** Standort: Luterbach Bilfinger Industrial Services Schweiz AG gehört zum Geschäftsfeld Industrial des Engineering - und Service-Konzerns Bilfinger SE. Das Unternehmen ist in der Schweiz an sechs Standorten vertreten. Die Kerngeschäfte sind die Instandhaltung, der Rohr **Dein Aufgabengebiet** - Durchführung und...