Manufacturing Associate II
vor 3 Wochen
About This Role
As a Senior Manufacturing Associate II, 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 facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and process controls. Individual will maintain training to the required level and support other functions on site.
What You’ll Do
- Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation
- Perform troubleshooting/investigation of equipment and process issues
- Revises documents as instructed, Capable of equipment and/or process changes
- Actively participates in training activities, managing their individual training plan and train other associates as required.
- Executes validation protocols
- Capable of leading shift when supervisor is absent, and actively leads or participates in shift
- exchanges. Coordinates activities and daily schedules with cross-functional areas.
- And other job duties that may be assigned from time to time
Who You Are
You are a highly skilled professional with expertise in manufacturing/technical processes and a deep understanding of scientific principles. Your analytical skills make you adept at troubleshooting and investigations. You excel in taking the lead on operational initiatives and projects, requiring minimal supervision. Your impact extends across multiple business units, showcasing your ability to navigate diverse organizational landscapes with a dynamic blend of technical acumen and leadership capabilities.
Required Skills
- High school diploma or equivalent as a minimum. Bachelor’s degree or higher preferred. Other combinations of education and experience can be considered
- Exceptional attention to detail and documentation skills.
- Exposure to Delta V or Syncade or similar automated systems
- Experience in highly regulated industry
- Languages: English B1, German and/or French an asset
Why Biogen?
Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts
-
Manufacturing Associate II
vor 4 Wochen
Luterbach, Schweiz Biogen International GmbH VollzeitAbout This Role As a Senior Manufacturing Associate II, 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 facilities. The...
-
Quality Control Associate Ii Microbiology
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description** About This Role** The main responsibilities for the Quality Control Associate II Microbiology includes execution of all the Microbiology related testing activities at Biogen’s large scale manufacturing facility in Solothurn, Switzerland. Microbiology related analysis at the site will include microbiological identification, bacterial...
-
Manufacturing associate V
vor 2 Wochen
Luterbach, Schweiz Biogen VollzeitAbout 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 associate is...
-
Manufacturing Upstream Associate Iii
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description**: **About This Role** 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...
-
Manufacturing Upstream Associate III
vor 2 Wochen
Luterbach, Schweiz Biogen VollzeitJob 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....
-
Manufacturing Associate IV
vor 2 Wochen
Luterbach, Schweiz Biogen VollzeitAbout 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...
-
Manufacturing Upstream Associate Iv
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description**: **About This Role** As a Manufacturing Upstream Associate IV, you'll perform processing steps and upstream 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...
-
Senior Associate II, QA Downstream
Vor 5 Tagen
Luterbach, Schweiz Biogen VollzeitJob DescriptionAbout This Role The Senior Associate II QA is being part of the Quality Compliance and Technical services team. This role is mainly responsible on Facility, Utilities and Equipment (FUE) Qualification and Validation at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/she is also responsible for the...
-
Senior Associate II, QA Downstream
Vor 3 Tagen
Luterbach, Schweiz Biogen VollzeitAbout This Role The Senior Associate II QA is being part of the Quality Compliance and Technical services team. This role is mainly responsible on Facility, Utilities and Equipment (FUE) Qualification and Validation at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/she is also responsible for the Quality...
-
Senior Associate II, QA Downstream
Vor 7 Tagen
Luterbach, Schweiz Biogen VollzeitJob DescriptionAbout This Role The Senior Associate II, QA Downstream will support the ongoing production and maintanance of the new Large Scale Manufacturing facility located in Luterbach, Switzerland.It is a technically orientated role requireing experience of the validation of production equipment and knowledge of production methodology involved in...
-
Senior Associate II, QA Downstream
Vor 6 Tagen
Luterbach, Schweiz Biogen VollzeitJob DescriptionAbout This Role The Senior Associate II, QA Downstream will support the ongoing production and maintanance of the new Large Scale Manufacturing facility located in Luterbach, Switzerland.It is a technically orientated role requireing experience of the validation of production equipment and knowledge of production methodology involved in...
-
Senior Associate II, QA Downstream
Vor 6 Tagen
Luterbach, Schweiz Biogen VollzeitAbout This Role The Senior Associate II, QA Downstream will support the ongoing production and maintanance of the new Large Scale Manufacturing facility located in Luterbach, Switzerland. It is a technically orientated role requireing experience of the validation of production equipment and knowledge of production methodology involved in...
-
Manufacturing Supervisor
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description**: **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...
-
Quality Control Associate I Microbiology
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description** About This Role** The main responsibilities for the Quality Control Associate I Microbiology includes execution of all the Microbiology related testing activities at Biogen’s large scale manufacturing facility in Solothurn, Switzerland. Microbiology related analysis at the site will include microbiological identification, bacterial...
-
Quality Control Associate I Microbiology
vor 4 Wochen
Luterbach, Schweiz Biogen International GmbH VollzeitAbout This Role The main responsibilities for the Quality Control Associate I Microbiology includes execution of all the Microbiology related testing activities at Biogen’s large scale manufacturing facility in Solothurn, Switzerland. Microbiology related analysis at the site will include microbiological identification, bacterial endotoxin test (KCA and...
-
Weigh & Dispense Associate Iii
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description**: **About This Role** Join our innovative team as a Weigh & Dispense Associate III, playing a crucial role in daily operations in a cGMP environment. You will be responsible for executing Weigh & Dispense manufacturing operations, managing material flow, and ensuring compliance to cGMP standards. As a detail-oriented professional with a...
-
Sr Materials Handler Ii
Vor 7 Tagen
Luterbach, Schweiz Biogen Vollzeit**Job Description**: **About This Role** Are you ready to take charge of GMP warehouse activities and play a pivotal role in the seamless execution of warehouse operations? As a Sr. Materials Handler II, you will be at the forefront, managing and ensuring the timely and accurate execution of all GMP warehouse activities. Your responsibilities will include...
-
Sr. Engineer II, Automation Core Systems
vor 2 Wochen
Luterbach, Solothurn, Schweiz Biogen International GmbH VollzeitAbout this roleAs Sr. Engineer II, Automation Core Systems, you will be responsible for providing engineering and technical leadership in support of Data Systems at the Solothurn site. Responsibilities include collaboration and building partnerships with site stakeholders and customers to ensure service levels and strategic direction align to the...
-
Sr. Engineer II, Automation Core Systems
vor 2 Wochen
Luterbach, Schweiz Biogen VollzeitJob DescriptionAbout this roleAs Sr. Engineer II, Automation Core Systems, you will be responsible for providing engineering and technical leadership in support of Data Systems at the Solothurn site. Responsibilities include collaboration and building partnerships with site stakeholders and customers to ensure service levels and strategic direction align to...
-
Sr. Engineer II, Automation Core Systems
vor 2 Wochen
Luterbach, Schweiz Biogen VollzeitJob Description About this role As Sr. Engineer II, Automation Core Systems, you will be responsible for providing engineering and technical leadership in support of Data Systems at the Solothurn site. Responsibilities include collaboration and building partnerships with site stakeholders and customers to ensure service levels and strategic...
