CSV Specialist at QRC Group Inc
Manatí, Puerto Rico, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

08 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Project Management Skills, Sat, Computerized Systems, English, Process Design, Training, Technical Documentation, Jmp, Scientific Analysis, Statistical Software, Statistics, Database, Gamp, Commissioning, Document Generation

Industry

Information Technology/IT

Description

Job Description

CSV SPECIALIST WITH EXPERIENCE IN BIOPROCESS VALIDATIONS.

Technical Skills:

  • Tech Transfer, Process Design, Commissioning & Qualification.
  • Vision system technologies (Strong).
  • Inspection/packaging Concepts.
  • Development and Execution of Processes/Equipment Characterization

Duties:

  • Provides data analysis/interpretation and assesses the impact of the data on the project.
  • Establish Testing Strategies.
  • Technical Reports Development.
  • Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies.

QUALIFICATIONS

  • BS or higher in Chemistry/ Biology/ Microbiology/ Computer Science/ Information Systems/Engineering or related discipline.
  • Background in pharmaceutical products manufacturing environment and in manufacturing and laboratories areas
  • More than five (5) years of experience working with process validation life cycle, experience in commissioning and validating laboratory and manufacturing computerized systems in a manufacturing environment, and training in validation methodologies, technologies, and process control computer systems.
  • Knowledge on computerized system with data collection software (database).
  • Strong knowledge of cGMP, GAMP, SAT, FDA, 21 CFR Part 11 and Data Integrity Regulations.
  • Experience in Automation process and/or Vision Inspection systems development.
  • Knowledge in statistics using Mini-tab, JMP or other statistical software, project management skills and knowledge in development documentation protocols and reports.
  • Knowledge in MS Project Management and MS Vision programs.
  • Advanced scientific analysis and troubleshooting skills.
  • Experienced in Instrument Performance qualification, and method configuration
  • Excellent skills writing commissioning/ validation, and technical documentation in English and using MS Office applications.
  • Bilingual (both English/Spanish)
    Additional Information
    All your information will be kept confidential according to EEO guidelines
Responsibilities
  • Provides data analysis/interpretation and assesses the impact of the data on the project.
  • Establish Testing Strategies.
  • Technical Reports Development.
  • Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies
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