Docutment Control Associate
Nutramax Laboratories, Inc. - Lancaster, SC

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The Document Control Associate is responsible for the management of technical documents, the maintenance of information systems, and the distribution of documents/batch records while ensuring accuracy of all documentation. Responsibilities include:
• Maintaining the document control systems for SOPs, batch records, and production process specifications
• Adhering to all cGMPs, SOPs, and policies
• Administering and maintaining change control systems
• Creating and issuing batch records for production
• Maintaining and monitoring quality system logbooks to ensure the timely completion of quality assurance processes
• Maintaining and filing master copy documents
• Administering the document archival process for off-site storage
• Collecting and reporting data for the Document Control Department
• Updating the electronic batch record program as necessary
• Checking work for accuracy to ensure no errors or deficiencies
• Performing other assigned duties that may be required to meet the company goals and objectives
Qualifications This position requires a high school diploma or GED. A minimum of 1 year experience in a Quality Assurance or cGMP environment preferred. Must be detail oriented, proficient in MS Office Suite and have good written/oral communication skills. Strong interpersonal skills and the ability to work well in a team environment is required. Additionally, this position is required use hands and arms to lift and reach. Must be able to lift/move packages and material weighing a minimum of 25 lbs.
Nutramax Laboratories has facilities in Maryland and South Carolina to meet our customer's needs and expectations.
Maryland Facility
Nutramax Laboratories, Inc.
2208 Lakeside Boulevard
Edgewood, MD 21040

South Carolina Facility
Nutramax Laboratories, Inc.
946 Quality Drive
Lancaster, SC 29720

Nutramax Laboratories, Inc. is an equal opportunity employer.