MedPharm Jobs in United States

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Project Manager · The Main Responsibilities of Project Managers at MedPharm include:Clients Engagement & Program Leadership: Serve as primary point of contact for clients. · Client Relations: · Build strong relationships with clients to ensure project success. · ...

Act as a lead analytical scientist on assigned studies assist with study plan review sample preparation chromatographic analysis data processing and interpretation and report writing. · ...

+This will be a global position leading and supporting the implementation, migration, validation, and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · +To effectively manage key Ph ...

The Stability Coordinator will be responsible for managing the stability program for the QC/R&D laboratories at MedPharm. · B.S with 4-6 years experience, or M.S with 2-3 years of experience. · 2-5 years´ experience in a GMP laboratory setting in the pharmaceutical industry · Exp ...

The Stability Coordinator will be responsible for managing the Stability program for the QC/R&D laboratories at MedPharm. · ...

This will be a global position leading and supporting the implementation migration validation and ongoing management of key electronic Quality Management Systems eQMS pharmaceutical computerized systems across MedPharm sites in UK and US ensuring equal support alignment across al ...

+Job summary · This will be a global position leading and supporting the implementation, migration, validation, and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · +To effectively ...

The Stability Coordinator will be responsible for managing the Stability program for the QC/R&D laboratories at MedPharm. · ...

The Project Manager plays a critical role in leading and executing client programs across MedPharm · This client-facing position ensures seamless project execution by coordinating internal teams, managing key project milestones, · and driving revenue through proactive scope manag ...

Act as a lead analytical scientist on assigned studies. Assist with study plan review, sample preparation, chromatographic analysis, data processing and interpretation, and report writing. · ...

The Scientist III/Sr. Scientist is responsible for developing and validating analytical methods to support drug formulation development in a GMP-compliant laboratory. · This role involves performing validations, stability testing, and forced degradation studies while ensuring dat ...

Act as a lead analytical scientist on assigned studies. Assist with study plan review, sample preparation, chromatographic analysis, data processing and interpretation, and report writing. · ...

The Quality Control Raw Materials Manager ensures that testing, data review, and documentation is compliant with GMP regulations. The ideal candidate will have superior communication skills and experience in a CDMO environment. · ...

This is a global position leading and supporting the implementation, migration, validation and ongoing management of key electronic Quality Management Systems (eQMS) and pharmaceutical computerized systems across MedPharm sites in UK and US. · ...

To perform experiments ensuring that projects are completed to plan while complying with all quality and safety regulations. · Assist or act as the lead scientist on assigned studies. · Draft study plans and contribute to the preparation of reports for sponsors. · ...

The Quality Control Raw Materials Manager ensures that testing data review and documentation is compliant with GMP regulations internal procedures and applicable compendial requirements. · Schedule the QC laboratory Raw Materials workload appropriately to meet manufacturing relea ...

The Quality Control Raw Materials Manager ensures that testing data review and documentation is compliant with GMP regulations internal procedures and applicable compendial requirements. · Minimum BA or BS in a scientific discipline required · Minimum of 5 years of prior supervi ...

To contribute to the upkeep of the R&D laboratory and ensure compliance with GxP regulations and MedPharm's procedures. · Industry experience or a science or engineering related degree. · ...

To perform experiments ensuring that projects are completed to plan while complying with all quality and safety regulations. · Assist with study plan writing data analysis and interpretation and report writing. · ...