Process Development Validation-Raw Material Associate

About this opportunity :

Process Development Validation-Raw Material Associate provides support to Avecia’s chemical raw material onboarding programs, including the Vendor Assurance Committee, and manage inventory databases.

Key Job Responsibilities:

• Process Chemistry support for the development and improvement of raw materials specifications with responsibility for managing the raw material management databases.
• Support identification of trends and action plans obtained from raw material release testing data.
• Process chemistry support to writing, reviewing, and revision of vendor assessment plans and reports.
• Responsible for reviewing new Process Validation protocol and report documents to support process development, manufacturing and validation activities.
• Review executed MFG batch records and PD experiment records to extract data for CPV and CSR activities.
• Process chemistry support to supplier audits and on-site supplier capability assessments when applicable.
• Support writing and maintenance of formal documents providing justification for specifications applied for release of raw materials.
• Coordinate raw material planning activities and raw material/engineering part inventory systems involving transactions in SAP.
• Report status of assigned activities to project teams and to Validation / Raw Material Development leadership on a weekly basis or as needed.
• Maintain an appropriate level of training on company and departmental procedures as determined by Avecia Raw Material Development.
• Adhere to all company environmental, health and safety policies to support raw material handling, storage and distribution practices.

Job Knowledge Required:

• BS in Scientific Discipline and 2 years of experience in related field within a chemical development or manufacturing environment.
• Sufficient knowledge of organic chemistry procedures, concepts, and literature.
• Demonstrated proficiency in preparation of technical reports and publications in English language.
• Experience in cGMP preferred.

The annualized salary range for this role is $68,000-$83,000.