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Sr. Validation Scientist 33160 - 1890093

๐ŸŒŸ Job Opportunity: Senior Validation Scientist 33160 - (Pharmaceutical Environment) ๐ŸŒŸ

Location: Residents of Puerto Rico

Period: Approximately 4 months by contract with ProQuality Network

Work Setup: Virtual/Remote with hybrid availability if needed by client

Shift: Mostly regular business hours (8:00 AM to 5:00 PM) but may vary for Process Validation executions


Summary:

Independently provides technical validation engineering support for process and equipment upgrades, replacements, and modifications in laboratory, manufacturing, or manufacturing support environments.


Preferred Qualifications:

  • Experience in validation, especially in Process Validation
  • Experience in biotechnology, pharmaceuticals, or medical devices industry


Knowledge:

  • Advanced validation knowledge (equipment qualification, cleaning, sterilization) ๐Ÿ”ฌ
  • Extensive technical expertise in validation ๐Ÿงช


Functions:

  • Troubleshoot systemic validation issues ๐Ÿ’ก
  • Apply advanced validation engineering principles to major system/process modifications ๐Ÿ› ๏ธ
  • Develop, analyze, and present results for operational issues/projects ๐Ÿ“Š
  • Complete complex assignments, develop new validation techniques ๐Ÿงช
  • Create validation policies affecting multiple units ๐Ÿ“œ
  • Supervise and review work of engineers/technicians ๐Ÿ‘ฉโ€๐Ÿ”ฌ
  • Employ advanced validation techniques within expertise ๐Ÿš€
  • Apply validation knowledge to diverse assignments ๐Ÿ“š
  • Develop technical solutions to complex problems ๐ŸŒ
  • Collaborate with various departments for process modifications ๐Ÿค
  • Ensure validation responsibilities in projects are met โณ
  • Develop departmental/project budgets ๐Ÿ’ฐ
  • Maintain regular attendance ๐Ÿ—“๏ธ


Problem Solving:

  • Provide practical solutions to difficult problems ๐Ÿค”
  • Solutions align with organizational objectives ๐ŸŽฏ


Discretion/Latitude:

  • Determine technical objectives with considerable latitude ๐ŸŒฑ
  • Work reviewed for desired long-term results โณ
  • Supervision relates to overall objectives and critical issues ๐Ÿ“ˆ


Impact:

  • Essential to broad programs/projects ๐ŸŒ
  • Decisions impact program schedules and resource utilization ๐Ÿ“Š


Leadership:

  • Lead group efforts, supervise staff/resources ๐ŸŒŸ
  • Guide completion of major programs/projects ๐Ÿš€


Liaison:

  • Prime technical contact for contracts/projects ๐Ÿค
  • Interact with senior personnel on technical matters ๐Ÿ“ž


Regulatory:

  • Understand industry trends and regulatory requirements ๐Ÿ“
  • Represent organization as technical expert ๐Ÿ†


Education/Licenses:

  • Doctorate/Master's degree + 3 years exp.
  • Bachelor's degree + 5 years exp.
  • Associate's degree + 10 years exp.
  • High school diploma/GED + 12 years exp. ๐Ÿ“š


Competencies/Skills:

  • In-depth knowledge of validation processes ๐Ÿ“œ
  • Effective communication and collaboration skills ๐Ÿ—ฃ๏ธ
  • Ability to handle multiple projects ๐Ÿ”„
  • Project management and leadership skills ๐Ÿ—๏ธ
  • Problem-solving and decision-making abilities ๐Ÿค”
  • Financial analysis and budget management skills ๐Ÿ’ฐ
  • Delegation and team management skills ๐Ÿ‘ฅ


Join us in advancing validation engineering in the Pharmaceutical Environment! ๐Ÿš€ Apply now and be part of our innovative team! ๐Ÿ’ผ


Thank you. We will be in contact soon.

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