QA Document Specialist - 10am - 6:30pm - Nutramax Laboratories

Summary of the Position: The QA Document Specialist I will understand the control, issuance, review, and maintenance of batch records, forms, and other pertinent cGMP documents and logbooks. QADS I will be able to solidly perform in primary tasks (either batch record review or document control) and able to assist in secondary tasks at assigned building.

Roles and Responsibilities:

• Proficient in required SAP transactions pertaining to primary job functions.
• Oversee the issuance and maintenance of pertinent documentation at primary assigned building.
• Ensure all documentation is both accurate and complete before releasing to production and/or customer consumption, including all pertinent Quality Control documents at primary assigned building.
• Communicate accurate and up-to-date status reviews to appropriate personnel and update all necessary spreadsheets.
• Communicate effectively with all other departments within the organization to ensure timely issuance, execution and correction of records in the quality system.
• Regular attendance is required.
• Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
• Communicate effectively with your team, supervision and other departments within the organization and function within a team, promoting positive work environment

Minimum Requirements: This position requires a minimum of 2 years of experience in a GMP or pharmaceutical manufacturing environment, preferably in a QA setting. Must be detailed oriented, have a strong mathematical background, and possess strong organization skills with the ability to handle multiple projects. Strong written and verbal communication skills required. Must be strongly proficient in MS office suite, specifically Word and Excel. SAP experience is preferable but not required.

Education and Experience: Position requires an Associate Degree or a minimum of two years' experience in QA related to food, pharmaceutical, or other government related industry.

Supervisory Responsibilities: None