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GSK

Develops medicines, vaccines, and consumer health

Senior Manager Supplier Quality Audit Lead

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • At least 10 years of experience in a pharmaceutical or biological environment, including commercial and/or research and development operations.
  • Proficiency and experience in planning and executing audits to identify and reduce significant risks and non-compliances.
  • Knowledge of regional and global Good Manufacturing Practice (GMP) and GSK quality requirements, and the ability to explain and relate these requirements to GSK manufacturing and supplier operations using sound business judgment.
  • Awareness of the business environment and ability to build networks and relationships with third-party suppliers and internal stakeholders.
  • Influencing and negotiating skills to secure access for assessments and implementation of appropriate corrective actions.
  • Verbal and written communication skills to relay issues, risks, and opportunities effectively and enable parties to understand them and establish effective action plans.
  • Proficiency in verbal and written English.
  • Experience with Microsoft Office applications and ability to learn and apply new software applications, such as audit management software, artificial intelligence tools, and remote virtual meeting tools.
  • A graduate or postgraduate degree in a relevant science discipline (Biology, Chemistry, or Pharmacy), Food, Chemical, Biotechnology, or an equivalent engineering area of expertise.
  • Skills in data integrity, digital fluency, GxP regulations, influencing without authority, lean management, pharmaceutical regulatory compliance, problem solving, quality assurance, quality auditing, risk awareness, and technical writing.

Responsibilities

  • Perform Quality System assessments for assigned audits within the role’s scope, ensuring assessments are effectively prepared, conducted, and reported.
  • Make risk-based recommendations on GxP approval status and document assessments in relevant systems within targeted timelines.
  • Communicate transparently and openly with business stakeholders, providing timely updates on audit progress and potential issues throughout the audit lifecycle.
  • Agree appropriate corrective and preventive action (CAPA) plans and follow up on their completion within agreed timelines.
  • Ensure audit-related documentation is communicated within targeted timelines and CAPA-related documents are reviewed and answered within targeted timelines.
  • Maintain auditee profiles in relevant data systems and keep all assessment data current based on available information.
  • Collate identified risks and escalate high-risk issues or situations so management and stakeholders understand technical, regulatory, and quality risks and identify appropriate mitigations.
  • Complete relevant training curricula within the stipulated timeframe.
  • Follow relevant Quality Assurance and Compliance procedures.
  • Remain current with technical processes, industry trends, and changes in the regulatory and external environment as needed.

About the Company

GSK

Develops medicines, vaccines, and consumer health

GSK is a global healthcare company focused on three main areas: Pharmaceuticals, Vaccines, and Consumer Healthcare. It develops medicines, vaccines, and consumer health products to improve health outcomes worldwide. Its products address diseases in respiratory, HIV, oncology, and immuno-inflammatory areas; vaccines for influenza, shingles, and COVID-19; and over-the-counter wellness products. The company relies on substantial R&D and strategic partnerships to bring new products to market and to address health needs. Revenues come from sales of medicines, vaccines, and consumer health items, often complemented by patient support programs and collaborations with governments and biotech partners.

Company size
10,001+
Company stage
IPO
Headquarters
London, United Kingdom
Founded
1891

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