Job Summary The Quality Assurance Engineer is responsible for supporting the Quality Assurance department for the operations of a pharmaceutical manufacturing facility. The individual must have the ability to write reports clearly, concisely and accurately. The individual must have strong knowledge and application of the CFR’s, Events, Change Controls, Batch Reports, and cGMP’s. Responsibilities Assist with the integration and support of qualit...
Job Summary. The Quality Assurance Engineer is responsible for supporting the Quality Assurance department for the operations of a pharmaceutical manufacturing facility. The individual must have the ability to write reports clearly, concisely and accurately. The individual must have strong knowledge and application of the CFR’s, Events, Change Controls, Batch Reports, and cGMP’s. Responsibilities. Assist with the integration and support of qual...
cGMP Consulting, Inc. is seeking technical writers who would support engineers of all experience levels to provide technical support/ documentation to Engineering and Validation teams for facility, equipment, and utility (FUE) qualification for a variety of on-going projects in the pharmaceutical industry. Position activities include FUE commissioning, qualification, validation, risk assessments, troubleshooting, problem-solving, and ensuring com...
cGMP Consulting, Inc. is seeking technical writers who would support engineers of all experience levels to provide technical support/ documentation to Engineering and Validation teams for facility, equipment, and utility (FUE) qualification for a variety of on-going projects in the pharmaceutical industry. Position activities include FUE commissioning, qualification, validation, risk assessments, troubleshooting, problem-solving, and ensuring com...
. The Environmental Health & Safety (EHS) Associate will support the facility with ISO certification process for multiple facilities within a global pharmaceutical manufacturing company. This person will be responsible for conducting risk management assessments, facilitating ISO facility audits and certifications, and creating and maintaining ISO-related documentation, among other duties. Responsibilities. Manage and maintain company's ISO 14001,...
Summary. cGMP Consulting, Inc. is seeking an individual to coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations and discrepancies. Oversee and review validation area processes. cGMP Consulting is looking for an individual who is efficient, comfortable working independently, and who will handle multiple projects and priorities, work with ti...
Summary. cGMP Consulting, Inc. is seeking an individual to coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations and discrepancies. Oversee and review validation area processes. cGMP Consulting is looking for an individual who is efficient, comfortable working independently, and who will handle multiple projects and priorities, work with ti...
