Summer Intern – GMP Quality - Newton, MA

In this role you will support the Quality function at C4 Therapeutics with a keen focus on GMP Quality Assurance. · You will oversee the manufacturing and testing of clinical trial material, including quality control and other types of analytical testing, and support for the Qual ...

In this role, you will support the Quality function at C4 Therapeutics, with a keen focus on GMP Quality Assurance. Assure quality support and oversight for the manufacture, testing, packaging, and product disposition of clinical trial materials ensuring compliance with GxP regul ...

As a Karyopharm intern you will positively impact patients' lives by assisting with Quality Unit efforts and activities within the organization and the Contract Service Providers. · ...

As a Karyopharm reporting to the Executive Director , GMP (Good Manufacturing Practice) · Quality you will positively impact patients' lives by: · ...

The GMP Operational Quality Senior Manager will lead and oversee quality operations supporting GMP manufacturing activities. This role is responsible for driving compliance, managing complex quality investigations, leading cross-functional teams, and ensuring quality systems are ...

We're seeking an Associate Director of GMP Quality Assurance to provide quality oversight for Oruka's clinical development programs and manufacturing. · The successful candidate will ensure compliance with phase-appropriate regulatory requirements applicable guidelines industry b ...

The Associate Director of GMP Quality Assurance will report to the Senior Director of GMP Quality. · ...

Oruka Therapeutics seeks an Associate Director of GMP Quality Assurance to provide quality oversight for clinical development programs and manufacturing. · Provide GMP quality support and guidance · Review and approve documentation · Investigate deviations and CAPAs · ...

The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. The Quality Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects. · ...

Xenon Pharmaceuticals is seeking an Associate Director of Quality Assurance for its GMP operations in Boston, MA. The successful candidate will have experience with global GMP regulations and principles. · ...

+Job summary · The Director will oversee GMP QA operations including batch disposition process across CDMOs in the US and Internationally. · +ResponsibilitiesDay-to-day operational quality oversight for internal batch record review operations. · QA manufacturing operations from c ...

The Director, Quality Assurance GMP Operations will oversee the GMP QA operations including batch disposition process across CDMOs in the US and Internationally. · Oversight of internal and external quality operations for batch disposition. · Continuous improvement of processes t ...

The Quality Manager coordinates activities on a wide range of projects and takes a role in the design and execution of new projects. · Key Duties And Responsibilities · Perform change control assessments and closure approvals · ...

The Manager, GMP Quality Assurance will be responsible for supporting late-stage GMP QA activities and transitions through PPQ to commercial launch. This includes overseeing master and executed batch record review and disposition of drug substances and drug products. · Support cr ...

The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. · The role will also have responsibilities associated with QC data review for both non-routine and routine cGMP process testing and in support of stability testing o ...

The Quality Specialist will provide QA support for manufacturing operations, · analytical laboratory operations, and materials management. · Review & support activities related to product disposition. · Solve nonconformance events by applying deviation management procedure. · ...

The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. · ...

The Quality Manager is responsible for ensuring compliance with cGMPs policies and procedures while performing activities on the floor in support of batch records review and disposition. · Key Duties include leading root-cause analysis investigations, change control assessments c ...

The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. · ...

The Quality Manager is a technical resource in the principles and application of quality assurance and compliance. · This position performs and leads activities on the floor in support of batch records review and disposition while ensuring compliance with cGMPs policies and proce ...