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Accenture

Advises businesses and runs their technology

Full Stack Engineer

Regulatory & Quality (Life Sciences)Posted on Nov 12
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • At least 5 years of experience is listed as a minimum requirement; the additional information separately states a minimum of 7 years of experience.
  • A Bachelor of Engineering degree or equivalent academic credential is required, along with 15 years of full-time education.
  • Knowledge of Computer System Validation (CSV) is required.
  • Global regulatory knowledge in pharmaceutical regulatory compliance and Computer System Validation (CSV)/Computer Software Assurance (CSA), including knowledge of FDA and other global regulatory bodies such as EMEA.
  • Comprehensive knowledge of the full-cycle Computer System Validation process in GxP environments, including hands-on experience with the V-Model and the complete validation lifecycle for regulated projects.
  • Knowledge of 21 CFR Part 11 and GAMP5 guidelines.
  • Ability to author, develop, and refine Standard Operating Procedures (SOPs) and Work Instructions.
  • GxP awareness and adherence to Good Documentation Practices (GDP).
  • Practical experience preparing for, participating in, and supporting external regulatory audits.
  • Analytical capabilities, clear communication skills, leadership qualities, problem-solving, and troubleshooting abilities.
  • Ability to collaborate with diverse teams and stakeholders to gather and validate requirements.
  • Ability to address challenges during process design and implementation, and familiarity with regulatory and compliance considerations related to system validation.

Responsibilities

  • Develop and/or engineer end-to-end system features, from user experience through backend code, using development skills to deliver solutions for clients.
  • Apply new technologies to challenging business problems with a cloud-first and agile mindset.
  • Guide and manage small teams while actively performing and overseeing project validation activities.
  • Represent the compliance/validation team as the primary liaison during internal meetings, gather data, and report compliance metrics to management.
  • Coach and mentor team members to support consistent understanding and execution of client workflows and project validation targets.
  • Maintain a comprehensive and up-to-date understanding of FDA and other global regulatory guidelines.
  • Develop Standard Operating Procedures (SOPs) and support external regulatory audits.

About the Company

Accenture

Advises businesses and runs their technology

Accenture advises large businesses and public agencies on strategy, builds their technology systems and runs ongoing operations. Its teams connect business planning with implementation, covering areas such as cloud migration, cybersecurity and customer experience. Consultants work with clients to redesign processes, while engineers integrate software from technology partners and maintain the resulting systems for multinational organizations. Clients pay for project work or continuing services, including application support and business processes such as finance and customer service. Accenture was founded in 1989 and has its headquarters in Dublin, Ireland.

Company size
10,001+
Company stage
IPO
Headquarters
Dublin, Ireland
Founded
1989

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