Process Development Sr. Scientist

QRC; Juncos (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

QRC Group, LLC in the United States seeks a Process Development Sr. Scientist to support scientific and technical activities within a regulated manufacturing environment.

The ideal candidate has a strong science background and experience with validation activities, technical documentation, and cross‑functional collaboration. Responsibilities include contributing to process development, process improvement, filling validation activities, and ensuring compliance with regulatory standards.

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.
• Filling validation experience.
• Experience working on technical documentation.
• Fully bilingual (English and Spanish)

Responsibilities

• Support process development and improvement in a regulated manufacturing environment.
• Contribute to validation activities and ensure proper technical documentation.
• Collaborate across cross-functional teams to meet regulatory compliance initiatives.

Skills

Validation experience

Filling validation experience

Technical documentation

Bilingual English and Spanish

Education

Engineering or Microbiology

PhD/PharmD/MD

Master’s degree with 3+ years

Bachelor’s degree with 5+ years

Job description

Company Description

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 a

Company 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 a Process Development Sr. Scientist to 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

Requirements

• 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.
• Filling validation experience.
• Experience working on technical documentation.
• Fully bilingual (English and Spanish)

Additional Information

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