Process Development Sr. Scientist

QRC Group, Inc

Juncos (PR)

On-site

USD 90,000 - 130,000

Full time

7 days ago
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Job summary

QRC Group, LLC seeks a Process Development Sr. Scientist to support scientific and technical activities within a regulated manufacturing environment. The ideal candidate will contribute to process development, process improvement, and compliance-driven initiatives while ensuring robust technical documentation.

The role requires a strong scientific background and validation experience, with full bilingual proficiency in English and Spanish to coordinate across multilingual teams.

Qualifications

  • Education in Engineering or Microbiology.
  • Doctorate (PhD, PharmD, or MD); or Master’s degree with 3+ years of scientific experience; or Bachelor’s degree with 5+ years of scientific experience.
  • Validation experience in a highly regulated industry.
  • Experience working on technical documentation.
  • Fully bilingual (English and Spanish).

Responsibilities

  • Support scientific and technical activities in a regulated manufacturing environment.
  • Contribute to process development, process improvement, and compliance initiatives.
  • Assist with creation and maintenance of technical documentation.

Skills

Process development
Validation experience
Technical documentation
Bilingual English/Spanish

Education

Engineering or Microbiology

Job description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Job Description

We are seeking aProcess Development Sr. Scientistto support scientific and technical activities within a regulated manufacturing environment. The ideal candidate will possess a strong scientific background, experience with validation activities, technical documentation, and the ability to contribute to process development, process improvement, and compliance-driven initiatives.

Qualifications
  • Education in Engineering or Microbiology.
  • Doctorate (PhD, PharmD, or MD); or Master’s degree with 3+ years of scientific experience; or Bachelor’s degree with 5+ years of scientific experience.
  • Validation experience in a highly regulated industry.
  • Experience working on technical documentation.
  • Fully bilingual (English and Spanish)
Additional Information

All your information will be kept confidential according to EEO guidelines.

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