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Ashland

Specialty chemicals provider for coatings, pharma

Quality Assurance Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWilmington, DE, USANo salary listedIn-person

About the Job

Requirements

  • A Bachelor of Science degree in chemistry or biology, or equivalent years of experience.
  • At least 5 to 8 years of Quality Assurance experience in a regulated industry.
  • Ability to work as part of a team.
  • Competency in the use of Microsoft Office Suite.
  • Experience with SAP and iLIMS.
  • Knowledge of Laboratory current Good Manufacturing Practices, Good Laboratory Practice, and safety.
  • Strong written and oral communication skills, with the ability to read, interpret, and report data.

Responsibilities

  • Maintain and continuously improve site quality procedures and the quality management system.
  • Support compliance with ISO 9001, current Good Manufacturing Practices, and applicable site quality standards.
  • Maintain accurate, controlled, and audit-ready quality documents in accordance with good documentation practices.
  • Promote data integrity and uphold ethical standards in testing, research, and reporting.
  • Prepare, update, and maintain quality and regulatory documentation, including Standard Operating Procedures, work instructions, and Drug Master File support documents.
  • Conduct internal quality and current Good Manufacturing Practices audits, gap assessments, and compliance reviews.
  • Perform risk assessments to identify potential hazards, evaluate compliance risks, and implement appropriate controls.
  • Investigate deviations, out-of-specification results, and customer complaints; identify root causes and recommend corrective actions.
  • Support management of change activities and quality-related validation projects.
  • Conduct supplier risk assessments and support supplier qualification and approval activities.
  • Evaluate raw materials for quality and regulatory compliance.
  • Review batch records and complete final product release activities in iLIMS and SAP.
  • Manage the product stability program, including sample coordination, data review, and documentation.
  • Coordinate raw-material and finished-product retesting as required.
  • Review product compliance against applicable compendial and global monograph requirements.
  • Maintain records and coordinate submissions for new Halal and Kosher product certifications.
  • Provide regulatory intelligence and documentation support for site products and initiatives.
  • Respond promptly and accurately to quality- and regulatory-related customer inquiries and documentation requests.
  • Set up new products in iLIMS and maintain accurate product master data.
  • Support qualification of new laboratory equipment and associated documentation.
  • Provide backup support to the Quality Control laboratory and inspect samples to verify consistent product quality.
  • Monitor quality metrics, analyze trends, and communicate findings to support informed decision-making.
  • Identify potential sources of error and recommend practical improvements to strengthen quality, reliability, and efficiency.
  • Collaborate cross-functionally with laboratory, manufacturing, regulatory, supply chain, and other site teams.
  • Support quality and Environmental, Health, and Safety good-catch programs and related improvement initiatives.

About the Company

Ashland

Specialty chemicals provider for coatings, pharma

Ashland is a diversified specialty chemicals company that originated as an oil refinery in 1924 and gradually shifted into chemicals, construction, and coal before fully reinventing itself as a pure-play specialty chemicals provider. Its products serve the personal care, pharmaceutical, and coatings markets. The company operates by developing and supplying chemical ingredients used in formulations across these industries, rather than delivering consumer finished goods. Compared with competitors, Ashland focuses on specialty chemical ingredients with an emphasis on performance materials and advanced additives, supported by a history of strategic acquisitions and spin-offs that steered it away from refining into differentiated chemical solutions. The company’s goal is to grow as a leading supplier of high-value, specialty ingredients by applying chemistry to improve the performance and quality of its customers’ products.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Covington, KY
Founded
1924

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