Senior Manufacturing Associate

Job Summary:Perform and document daily manufacturing operations in a cGMP environment, including operating process equipment, executing validation protocols, and revising cGMP documentation. Ensure compliance with cGMP standards while maintaining equipment and facilities. This role requires strong attention to detail and expertise in automated systems and...

Summary: Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents. Ensuring compliance to cGMP as well as maintaining equipment and facilities. The MA is detailoriented with strong documentation skills. Maintain training level to the...

The Manufacturing Associate (m/f/d) will be responsible for the following task area: Conducts and documents daily manufacturing operations in a cGMP environment and ensuring complianceOperate and maintain production equipment and facilities in a safe and efficient mannerFollow safety protocols and maintain a clean and organized work environment Depending on...

Job Summary:Are you ready to play a pivotal role in our mission?As a Supervisor Manufacturing, you'll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence and...

On behalf of our Pharmaceutical client based in Solothurn, we are looking for a Quality Control Associate.The Quality Associate assures that all operations meet or exceed cGMP regulations. The position needs reactive support of discrepancy identification. This position will support quality key metrics and analysis. This role is expected to be...

Aufgrund unserer Expansionspläne benötigen wir talentierte Mitarbeiterinnen und Mitarbeiter am Standort Solothurn in der Abteilung Manufacturing, die bereit sind, Verantwortung zu übernehmen und unser Unternehmen in neue Märkte zu führen.**Kunststofftechnologe/-in | **100%**:Ref-Nr. 6920- Arbeitsort:- SolothurnEntwickeln Sie sich zusammen mit uns weiter...

Senior Regional Planner TECA (m/w/d WDescriptionAre you good at organizing knowledge and connecting connections? Do you enjoy keeping things in order and making sure everything makes logical sense? Are you one of those people who are willing to find solutions to complex problems and keep a cool head when the requests pile up? Would you like to use these...

Senior Regional Planner TECA (m/w/d WDescriptionAre you good at organizing knowledge and connecting connections? Do you enjoy keeping things in order and making sure everything makes logical sense? Are you one of those people who are willing to find solutions to complex problems and keep a cool head when the requests pile up? Would you like to use these...

For our client, an international company in Solothurn, we are looking for a Senior QA Release LeadStart date: End: Extension: must be discussedWorkplace: BaarWorkload: 100%Job SummaryAct as Responsible Person (RP) delegate for Commercial Biologics Drug Substances (DS), Parenteral Drug Products (DP), Parenteral Finished Goods (FG) technical release or Active...

Kraftort. Ypsomade. Aufgrund unserer Expansionspläne benötigen wir talentierte Mitarbeiterinnen und Mitarbeiter am Standort Solothurn in der Abteilung Manufacturing, die bereit sind, Verantwortung zu übernehmen und unser Unternehmen in neue Märkte zu führen. Kunststofftechnologe/-in | % Ref-Nr. 0 Arbeitsort: Solothurn Entwickeln Sie sich zusammen mit...

Job Description:The Senior Director of CMC Commercial Assets sits within the Pharmaceutical Operations & Technology team (PO&T) and is responsible for the end-to-end strategy of all commercial assets in all therapeutic areas and all modalities. Reporting to the VP of Asset Development and Portfolio Management, this Senior Director will have direct...

Omnichannel Capability Specialist WDescriptionOmnichannel Capability Specialist – Johnson & Johnson Zuchwill, SwitzerlandJnJ Medical Devices EMEA is recruiting for an Omnichannel Capability Specialist in Switzerland.As an Omnichannel Capability Specialist, you will be part of our EMEA Medical Devices Digital Operations Team and lead initiatives to design,...

Omnichannel Capability Specialist WDescriptionOmnichannel Capability Specialist – Johnson & Johnson Zuchwill, SwitzerlandJnJ Medical Devices EMEA is recruiting for an Omnichannel Capability Specialist in Switzerland.As an Omnichannel Capability Specialist, you will be part of our EMEA Medical Devices Digital Operations Team and lead initiatives to design,...

The Senior Manufacturing Associate (a) will be responsible for the following task area:Executing manufacturing processing steps and/or manufacturing support activitiesMonitoring upstream and downstream processesInvestigation and troubleshooting/adjustments of equipment/system setup if process issues ariseValidating protocols, and revising cGMP documentation...

For our client, an international company in Solothurn, we are looking for a Manufacturing Associate IVStart date: ASAPEnd: contract for 1 yearExtension: possibleWorkplace:SolothurnWorkload: 100%Please not that the position includes shift work : Shift work - 2 shift work / 5 shift work (with allowance)Job SummaryPerforms and documents daily manufacturing...

SUMMARY: Performs and documents daily Weigh & Dispense operations and internal material flow management activities in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents. Ensures compliance to cGMP as well as maintaining equipment and facilities. The associate is detail-oriented with strong...

**Summary**: Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents. Ensuring compliance to cGMP as well as maintaining equipment and facilities. The MA is detail-oriented with strong documentation skills. Maintain training level to the...

Manpower Switzerland is a leading provider of job placement services, helping over 20,000 men and women find permanent or temporary positions each year. With a network of over 5,000 client companies, ranging from SME's to multinationals, Manpower connects talented individuals with opportunities in various industries. The company is dedicated to providing...

**Summary**: - Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents. Ensuring compliance to cGMP as well as maintaining equipment and facilities. The MA is detail-oriented with strong documentation skills. Maintain training level to...

**Job Summary**: Perform and document daily manufacturing operations in a cGMP environment, including operating process equipment, executing validation protocols, and revising cGMP documentation. Ensure compliance with cGMP standards while maintaining equipment and facilities. This role requires strong attention to detail and expertise in automated systems...

**Job Summary**: Perform and document daily manufacturing operations in a cGMP environment, including operating process equipment, executing validation protocols, and revising cGMP documentation. Ensure compliance with cGMP standards while maintaining equipment and facilities. This role requires strong attention to detail and expertise in automated systems...

**Job Summary**: Are you ready to play a pivotal role in our mission? As a Supervisor Manufacturing, you'll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence...

**Job Summary**: Are you ready to play a pivotal role in our mission? As a Supervisor Manufacturing, you'll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence...

**Job Summary**: Are you ready to play a pivotal role in our mission? As a Supervisor Manufacturing, you'll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence...

**Job Summary**: Are you ready to play a pivotal role in our mission? As a Supervisor Manufacturing, you'll lead a dynamic team of Manufacturing Associates, ensuring the seamless execution of daily operations while upholding the highest standards of cGMP compliance and safety protocols. Your leadership will be instrumental in driving operational excellence...

The Manufacturing Associate (m/f/d) will be responsible for the following task area:Conducts and documents daily manufacturing operations in a cGMP environment and ensuring complianceOperate and maintain production equipment and facilities in a safe and efficient mannerFollow safety protocols and maintain a clean and organized work environmentDepending on...

The Manufacturing Associate (m/f/d) will be responsible for the following task area:Conducts and documents daily manufacturing operations in a cGMP environment and ensuring complianceOperate and maintain production equipment and facilities in a safe and efficient mannerFollow safety protocols and maintain a clean and organized work environmentDepending on...

The Manufacturing Associate (m/f/d) will be responsible for the following task area: Conducts and documents daily manufacturing operations in a cGMP environment and ensuring complianceOperate and maintain production equipment and facilities in a safe and efficient mannerFollow safety protocols and maintain a clean and organized work environment Depending on...

The Manufacturing Associate (m/f/d) will be responsible for the following task area: Conducts and documents daily manufacturing operations in a cGMP environment and ensuring complianceOperate and maintain production equipment and facilities in a safe and efficient mannerFollow safety protocols and maintain a clean and organized work environment Depending on...

On behalf of our Pharmaceutical client based in Solothurn, we are looking for a Quality Control Associate. The Quality Associate assures that all operations meet or exceed cGMP regulations. The position needs reactive support of discrepancy identification. This position will support quality key metrics and analysis. This role is expected to be...

On behalf of our Pharmaceutical client based in Solothurn, we are looking for a Quality Control Associate. The Quality Associate assures that all operations meet or exceed cGMP regulations. The position needs reactive support of discrepancy identification. This position will support quality key metrics and analysis. This role is expected to be...

General information: Contract: temporary Starting date: O1.05.2024 End date: 31.12.2024 (with extension possibility) The Associate II Quality Control is primarily responsible for managing various aspects of sample handling and documentation within the Quality Control department. This includes sample management, shipment coordination, ordering and...

Aufgrund unserer Expansionspläne benötigen wir talentierte Mitarbeiterinnen und Mitarbeiter am Standort Solothurn in der Abteilung Manufacturing, die bereit sind, Verantwortung zu übernehmen und unser Unternehmen in neue Märkte zu führen. **Kunststofftechnologe/-in | **100%**: Ref-Nr. 6920 - Arbeitsort: - SolothurnEntwickeln Sie sich zusammen mit uns...