Sr Quality Systems Specialist

Lancesoft

Warsaw (IN)

Remote

USD 90,000 - 130,000

Full time

8 days ago
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Job summary

Lancesoft seeks a Sr Quality Systems Specialist to lead and sustain the Quality Management System across sites, with focus on GMP, ISO, and EUMDR compliance. This remote role supports teams in the US, Colombia, and India while coordinating document control and process improvements.

You will assist audits, investigations, and external assessments, ensuring robust CAPA and cross-site information flow. A life sciences degree with relevant experience is preferred.

Qualifications

  • Bachelor's Degree and 4 years of relevant experience, or Associate's Degree and 6 years of relevant experience, or High School Diploma or Equivalent and 8 years of relevant experience
  • Bachelor's Degree in life sciences field with minimum 5 years of relevant work experience preferred

Responsibilities

  • Develop and implement processes, procedures, and instruction to sustain and improve the Quality Management System
  • Support Top Management in the development and implementation of quality systems strategies and objectives
  • Oversee and coordinate the communication and release of corporate documents for all sites
  • Develop and support site document control procedures and work instructions
  • Develop and execute process improvements to ensure Site Quality processes meet users needs and requirements
  • Coordinate project work related to integration of sites and migration to integrated systems.
  • Assist and lead audits and assessments, both internal and external, to demonstrate compliance with GMP, ISO, CMDR, and EUMDR regulations
  • Support Quality investigations as needed
  • Manage and facilitate external standard assessments

Skills

FDA regulations
EUMDR
Statistical analysis
Technical writing
MS Office
PowerBI
Adobe Acrobat
CAPA
Root cause analysis
Quality systems

Education

Bachelor's degree in life sciences
Associate's degree
High school diploma or equivalent

Tools

PowerBI
Adobe Acrobat
MS Office

Job description

Title: Sr Quality Systems Specialist

Location: Remote--looking for workers in US, Columbia, India

Duration: 12 Months

Duties
  • Develop and implement processes, procedures, and instruction to sustain and improve the Quality Management System
  • Support Top Management in the development and implementation of quality systems strategies and objectives
  • Oversee and coordinate the communication and release of corporate documents for all sites
  • Develop and support site document control procedures and work instructions
  • Develop and execute process improvements to ensure Site Quality processes meet users needs and requirements
  • Coordinate project work related to integration of sites and migration to integrated systems.
  • Assist and lead audits and assessments, both internal and external, to demonstrate compliance with GMP, ISO, CMDR, and EUMDR regulations
  • Support Quality investigations as needed
  • Manage and facilitate external standard assessments

This is not an exhaustive list of duties or functions and might not necessarily comprise all the essential functions.

Skills
  • Excellent working knowledge of current USA Food and Drug Administration (FDA) and global laws, regulations, and standards, particularly EUMDR
  • Familiarity with statistical data analysis tools and concepts
  • Ability to objectively deal with individuals using appropriate tact and diplomacy to establish and maintain a congenial relationship
  • Proficiency in technical writing
  • Outstanding organizational skills
  • Basic experience or knowledge on issue resolution disciplines (e.G. Problem solving/decision making, root cause analysis, etc.)
  • Must be able to manage stressful situations and to handle controversial issues
  • Must be familiar with all aspects and elements of a quality system including but not limited to corrective and preventive action (CAPA), management responsibility, product realization and measurement, analysis and improvement processes
  • Highly compliance-oriented to firmly adhere to the principles of the regulations and standards
  • High attention to detail
  • Demonstrated proficiency with MS Office suite, Adobe Acrobat, PowerBI and various data sources
Education

Bachelor's Degree and 4 years of relevant experience, or Associate's Degree and 6 years of relevant experience, or High School Diploma or Equivalent and 8 years of relevant experience

Bachelor s Degree in life sciences field with minimum 5 years of relevant work experience preferred

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