Manufacturing Associate Dispensary

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...

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

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

**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...

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...

**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...

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...

As a Quality Control Associate (a) you will be responsible for the sample management related activitiees:Coordinate movement and shipping of QC samples while ensuring confidentiality and adherence to standard operating procedures.Utilize LIMS and enterprise resource planning systems for sample management.Prepare shipment documents in collaboration with trade...

**Résumé du poste**: Vous êtes en charge de l'élaboration et de la mise en œuvre de la stratégie de développement de l'entreprise, de l'organisation et de la mise en œuvre de la politique de développement de l'entreprise. Il s'agit d'assurer la conformité aux normes cGMP tout en entretenant l'équipement et les installations. Ce rôle exige une...