Bengaluru, Karnataka, India On-site

Full-time · Mid-Senior level
1,001-5,000 employees · IT Services and IT Consulting

Experience : 2-4 years

Triaging the compiler bugs, analyze different aspects for the fix such as correctness/performance, and do the developmental fix verification for LLVM based compiler toolchain.
Have knowledge on advanced compiler optimizations, processor architecture specific tuning, and parallelization and vectorization approaches.
Have good understanding on LLVM like compiler toolchain system, usage, and thorough holds on different compilation options.
Familiarity with processor micro-architecture such as x86 x64 is advantages.
Knowing compiler toolchain techniques such as LTO, PGO, sanitizers, fuzzers are added advantages.
Have hands on C++ programming, and basics of Python.
Knowing usage of infrastructure support tools such as github, JIRA, Confluence, CMAKE are good.

Roles and Responsibilities:

Works closely with global Compiler development team, performance analysts, and the compiler related applications team.
Ensure the quality of the compiler by verifying all targeted bugs-fix are fixed and features are working as expected.
Support entire toolchain eco-system development and maintenance including compiler, linkers, other binary utilities by exhibiting proactive problems solving approach.
Support in betterment of compiler toolchain system by stretching and offering support in compiler toolchain development and testing.

Raritan, NJ 08869

Key Responsibilities:

QA oversight of LVV manufacturing process to ensure cGMP compliance.
Review Master Batch Records to confirm data is accurate, legible, and consistent with established GDP requirements.
Perform manufacturing documentation compilation and quality issue assessment for the release of Lentiviral Vector product.
Perform inspection and release of raw materials needed for LVV production, as required.
Support review, revision, or drafting Standard Operating Procedures (SOPs) for Quality department in relation to the LVV process.
Provide quality and compliance input for continuous improvement and corrective actions of GxP practices within the lentivirus vector manufacturing facility.
Collaborate in a team based, cross-functional environment to complete tasks required by shift schedule.
Maintain quality practices and perform tasks in accordance to state and federal regulatory requirements and cGMP requirements.
Collaborate with functional departments to resolve issues related to LVV production, batch review, and release.
Clear communication with other QA LVV team members, to ensure consistent performance, and identification of deviations.
Ensure readiness of records for regulatory inspections.
Review, compile, and organize data for trending.


Qualifications


Education:

Minimum of a Bachelor’s or equivalent University Degree in Science, Information Science, or equivalent technical field is required

Experience and Skills:

Required:

Minimum 4 years of relevant work experience
Experience in Quality Assurance and/or Quality Systems Compliance
Knowledge of cGMP and FDA regulations
Good written and verbal communication skills

Raritan, NJ 08869

Key Responsibilities:

QA oversight of LVV manufacturing process to ensure cGMP compliance.
Review Master Batch Records to confirm data is accurate, legible, and consistent with established GDP requirements.
Perform manufacturing documentation compilation and quality issue assessment for the release of Lentiviral Vector product.
Perform inspection and release of raw materials needed for LVV production, as required.
Support review, revision, or drafting Standard Operating Procedures (SOPs) for Quality department in relation to the LVV process.
Provide quality and compliance input for continuous improvement and corrective actions of GxP practices within the lentivirus vector manufacturing facility.
Collaborate in a team based, cross-functional environment to complete tasks required by shift schedule.
Maintain quality practices and perform tasks in accordance to state and federal regulatory requirements and cGMP requirements.
Collaborate with functional departments to resolve issues related to LVV production, batch review, and release.
Clear communication with other QA LVV team members, to ensure consistent performance, and identification of deviations.
Ensure readiness of records for regulatory inspections.
Review, compile, and organize data for trending.


Qualifications


Education:

Minimum of a Bachelor’s or equivalent University Degree in Science, Information Science, or equivalent technical field is required

Experience and Skills:

Required:

Minimum 4 years of relevant work experience
Experience in Quality Assurance and/or Quality Systems Compliance
Knowledge of cGMP and FDA regulations
Good written and verbal communication skills

Preferred:

Experience working with large molecules or Lentivirus vector production
Knowledge of Good Tissue Practice or experience with cell-based manufacturing
Experience working in an aseptic manufacturing facility
Knowledge of EU guidance

Other:

Requires ability and flexibility to accommodate unplanned overtime (including nights and weekends) on little to no prior notice

Raritan, NJ 08869

Key Responsibilities:

QA oversight of LVV manufacturing process to ensure cGMP compliance.
Review Master Batch Records to confirm data is accurate, legible, and consistent with established GDP requirements.
Perform manufacturing documentation compilation and quality issue assessment for the release of Lentiviral Vector product.
Perform inspection and release of raw materials needed for LVV production, as required.
Support review, revision, or drafting Standard Operating Procedures (SOPs) for Quality department in relation to the LVV process.
Provide quality and compliance input for continuous improvement and corrective actions of GxP practices within the lentivirus vector manufacturing facility.
Collaborate in a team based, cross-functional environment to complete tasks required by shift schedule.
Maintain quality practices and perform tasks in accordance to state and federal regulatory requirements and cGMP requirements.
Collaborate with functional departments to resolve issues related to LVV production, batch review, and release.
Clear communication with other QA LVV team members, to ensure consistent performance, and identification of deviations.
Ensure readiness of records for regulatory inspections.
Review, compile, and organize data for trending.


Qualifications


Education:

Minimum of a Bachelor’s or equivalent University Degree in Science, Information Science, or equivalent technical field is required

Experience and Skills:

Required:

Minimum 4 years of relevant work experience
Experience in Quality Assurance and/or Quality Systems Compliance
Knowledge of cGMP and FDA regulations
Good written and verbal communication skills

Preferred:

Experience working with large molecules or Lentivirus vector production
Knowledge of Good Tissue Practice or experience with cell-based manufacturing
Experience working in an aseptic manufacturing facility
Knowledge of EU guidance

Other:

Requires ability and flexibility to accommodate unplanned overtime (including nights and weekends) on little to no prior notice