Quality Assurance Associate
Nutrafol- Full Time
- Junior (1 to 2 years)
Candidates should possess a Bachelor’s degree in a relevant field, such as Quality Assurance, Document Control, or a related discipline, and have at least one year of experience in a quality-focused role within a pharmaceutical or medical device manufacturing environment. Familiarity with Current Good Manufacturing Practice (cGMP) standards and regulatory requirements is essential.
As an Associate - QA Doc cell, you will be responsible for managing document control activities, ensuring adherence to cGMP standards, reviewing and verifying GDP issues, issuing and closing logbooks, archiving executed records, verifying BMRs and BPRs, integrating product specifications, maintaining Bills of Material, and preparing annual product review reports. Additionally, you will participate in change control management, investigate non-conformances, and perform corrective and preventive actions, while also updating Standard Operating Procedures and collaborating with cross-functional teams.
Provides essential medical products and services
Baxter International provides a wide range of medical products and services essential for healthcare. The company operates in several areas, including critical care, hospital care, nutritional care, renal care, and surgical care. Its products are used in various settings, from emergency rooms to home healthcare, helping to meet the needs of patients and healthcare professionals. Baxter develops, manufactures, and distributes medical devices, pharmaceuticals, and biotechnology products, generating revenue through sales to healthcare providers and institutions. A key aspect that sets Baxter apart from competitors is its recent acquisition of Hillrom, which enhances its ability to offer comprehensive healthcare solutions. The company's goal is to improve care outcomes and increase access to healthcare through continuous innovation and a focus on patient needs.