Senior C&Q Engineer - GMP Compliance & Validation

Mentor Technical Group; Juncos (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading global life sciences consulting firm located in Juncos, Puerto Rico, seeks a professional to develop and maintain commissioning and qualification procedures. The ideal candidate will hold a Bachelor's or Master's degree in Chemical Engineering or Pharmaceutical Technology and have at least 2 years of GMP manufacturing experience. Fluency in English and strong analytical, problem-solving, and communication skills are essential. Join a collaborative team to ensure compliance and enhance quality in the pharmaceutical industry.

Qualifications

• Minimum 2 years of experience in GMP manufacturing.
• Strong understanding of regulatory requirements and quality standards.
• Proficiency in English; additional language skills are a plus.

Responsibilities

• Collaborate with C&Q Engineers to develop and maintain procedures.
• Write, review, and approve C&Q protocols and reports.
• Execute commissioning and qualification activities.

Skills

Collaborative teamwork

Analytical skills

Problem-solving

Regulatory knowledge

Communication skills

Education

Bachelor's or Master's in Chemical Engineering or Pharmaceutical Technology

Job description

A leading global life sciences consulting firm located in Juncos, Puerto Rico, seeks a professional to develop and maintain commissioning and qualification procedures. The ideal candidate will hold a Bachelor's or Master's degree in Chemical Engineering or Pharmaceutical Technology and have at least 2 years of GMP manufacturing experience. Fluency in English and strong analytical, problem-solving, and communication skills are essential. Join a collaborative team to ensure compliance and enhance quality in the pharmaceutical industry.