Manufacturing Associate Dispensary

Job SummaryThe Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities. This includes monitoring upstream and downstream processes, investigating and troubleshooting equipment/system setup if process issues arise, validating protocols, and revising cGMP documentation if...

The Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities, monitoring upstream and downstream processes, and investigating and troubleshooting equipment/system setup if process issues arise.To be considered for the role, the selected candidate must have technical education in...

The Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities, monitoring upstream and downstream processes, and investigating and troubleshooting equipment/system setup if process issues arise.Key responsibilities include validating protocols, revising cGMP documentation if...

The Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities, monitoring upstream and downstream processes, and investigating and troubleshooting equipment/system setup issues. They will also validate protocols, revise cGMP documentation as necessary, and operate and maintain...

The Senior Manufacturing Associate is responsible for overseeing the execution of manufacturing processing steps and supporting activities. Key tasks include monitoring upstream and downstream processes, investigating and troubleshooting equipment or system setup issues, validating protocols, and maintaining production equipment and facilities in a safe 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 detail-oriented with strong documentation skills. Maintain training level to the...

**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...

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:As a Senior Manufacturing Associate at Michael Page, you will be responsible for overseeing the manufacturing process and ensuring the highest quality standards are met. Your technical expertise and leadership skills will be essential in driving the success of our production team.Key Responsibilities:Executing manufacturing processing steps...

The Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities, monitoring upstream and downstream processes, and investigating and troubleshooting equipment/system setup issues. They will also validate protocols, revise cGMP documentation, and operate and maintain production...

**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 and...

Key Responsibilities:Oversee the execution of manufacturing processing steps and support activities to ensure compliance with industry regulations and company standards.Monitor upstream and downstream processes to identify areas for improvement and implement adjustments as necessary.Investigate and troubleshoot equipment and system setup issues to resolve...

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...

Manages and ensures a timely and accurate execution of all GMP warehouse activities. Receives goods and enters them into Oracle (OPM), supports preparation of goods for manufacturing (order picking), and ships finished goods, raw materials, and samples out from the site.Responsible for generic and non-GMP receipts and shipments.Accountability...

**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...