MedPharm

2 months ago

Quality Engineer II-III, Quality Assurance

Open 59d North America

FMEA Regulatory Compliance Risk Assessment Root Cause Analysis

The Quality Engineer designs and maintains the Quality Management System for pharmaceutical manufacturing, ensuring compliance with GMP standards. They manage deviations, CAPA, validation protocols, and internal/external audits to support product quality and regulatory readiness.

Open 76d North AmericaSenior

Chemist III/Sr. Chemist Raw Materials

Position Summary – The Chemist III/Sr. Chemist Raw Materials ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The…

LIMS Program Management

QC Chemist II

Open 83d North America

Performs GMP-compliant analytical testing (HPLC, GC, titrations) in a pharmaceutical CDMO lab, documents results, and troubleshoots deviations.

GCP Regulatory Compliance Risk Assessment Root Cause Analysis

QA Specialist

Open 92d UKContract

QA Specialist ensures pharmaceutical manufacturing and lab processes meet GMP, GCP, and GLP standards by reviewing documentation, managing quality systems, and supporting compliance audits in Guildford, UK.

QC Chemist I-II, Raw Materials

Open 86d North America

A QC Chemist I tests raw materials and packaging components using techniques like HPLC, GC, and titrations to ensure compliance with GMP regulations and internal procedures in a pharmaceutical lab environment.

LIMS Program Management

Associate Scientist, Analytical

Open 100d

General Information Title: Associate Scientist Department: Analytical Site: Guildford Reporting To: Team Leader Position Summary The Associate Scientist (Analytical) plays a key role in supporting research and…

Risk Assessment

Cleaning Validation Engineer

Open 99d North America

FMEA Risk Assessment Root Cause Analysis Technical Writing

Position Summary – The Cleaning Validation Engineer oversees the development, maintenance, and governance of MedPharm’s site-wide cleaning validation program across the full product lifecycle, from development through…

Environmental Health & Safety Manager

Open 99d North America

Corrective Action Emergency Response EPA FMEA Hazard Identification +10 skills

Job Purpose: The Manager of EHS is responsible for leading the Environmental Health and Safety programs and activities in support of MedPharm US sites, including the GMP pharmaceutical manufacturing site and the…

Open 99d North AmericaSenior

Sr. Director, Quality Control & Analytical Development

Position Overview The Sr. Director, Quality Control and Analytical Development provides strategic, technical, and operational leadership to the site Quality Control and Analytical Development Laboratories. This role…

Program Management

Open 112d North AmericaFull-time

5 months ago

Project Manager

Business Development PMP Salesforce Smartsheet

Project Manager Onsite | Durham, NC | Full-Time Position Summary – The Project Manager plays a critical role in leading and executing client programs across MedPharm’s end-to-end CDMO services. This client-facing…