Document Quality Specialist

Azzur Group is a premier consulting firm specializing in providing innovative solutions to the life sciences industry. Our expertise in quality assurance ensures that our clients' products, processes, and systems meet the highest standards of quality and regulatory compliance. Join us and contribute to projects that enhance product safety, efficacy, and reliability while working in a dynamic and collaborative environment.

We are seeking a detail-oriented and experienced Quality Assurance Specialist to join our consulting team. The Quality Assurance Specialist will be responsible for ensuring that products and processes comply with regulatory requirements and industry standards. The ideal candidate will have a strong background in quality assurance, excellent analytical skills, and a commitment to maintaining high standards of quality and compliance.

Key Responsibilities:

• Develop, implement, and monitor quality assurance processes and procedures to ensure...

FEFA LLC has an immediate need for a full-time, Document Quality Specialist for one of our Federal Government contracts in Silver Spring, MD.  The position is 100% on site at White Oak.

Position Summary:

• Analyze incoming documents and reports for completeness and compliance with the customer's guidelines and take appropriate steps to capture the pertinent information into databases and IT systems.
• Perform accurate and timely data entry using multiple screens in customer's system and classify/index/assign the records appropriately.
• Maintain paper and electronic records in accordance with customer's established guidelines.
• Perform document entry services, data analysis, tracking services, and stakeholder/user support
• Handle phone calls and emails from internal and external stakeholders and the public
• Perform data quality assurance (QA) and quality control (QC) with critical...

Quality Assurance and Document Compliance Specialist

80K Plus Benefits

Work Onsite 5 Days A Week

Great Neck, NY

Wholesale Food and Beverage Company is seeking a skilled FSQA Compliance Specialist, with experience evaluating document compliance of supply vendors. This position will work within the Food Safety and Quality Assurance Department, in the East Coast Headquarters, with an opportunity to become a leading member of an expanding team.

Responsibilities:

Review, assess, and evaluate the compliance status of both incumbent and new suppliers (knowledge of domestic and import processes is a plus).

Manage a high volume of audit reports from vendors with multiple subsidiaries and facilities requiring additional assessments.

Ensuring compliance with Importer of Record documentation.

Oversee Foreign Supplier Verification (FSVP)...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist, based onsite in our Tewksbury, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished...