Biopharma C&Q Engineer – Onsite (Juncos)

Avante Engineering; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Avante Engineering in Juncos, PR seeks a Commissioning & Qualification Scientist/Engineer to lead validation activities in Bio/Pharmaceutical environments. You will generate and execute validation documents, develop qualification protocols, and prepare comprehensive reports.

Ideal candidates combine a engineering or life sciences background with hands-on CQ experience, strong collaboration skills, and fluent English and Spanish communication. This in-person role requires relocation to PR.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• Experience in Bio/Pharmaceutical industry.
• Proficient in Commissioning & Qualification documentation.
• Strong analytical thinking and problem-solving skills.
• Team-oriented and able to collaborate with cross-functional teams.
• Excellent English and Spanish written and spoken communication.

Responsibilities

• Generate and execute validation documents, including protocol creation and testing within the bio-pharmaceutical industry.
• Develop qualification protocols for new or modified manufacturing equipment, utilities, and facilities.
• Prepare comprehensive summary reports based on validation and qualification test results.
• Provide support during implementation, collaborating with affected departments and personnel.
• Participate in progress meetings to ensure schedules are maintained and action items are addressed.

Skills

Analytical thinking

Problem-solving

Team collaboration

Documentation skills

Communication skills

Bilingual English/Spanish

Education

Bachelor’s degree in Engineering, Life Sciences, or related field

Tools

C&Q documentation

Job description

Avante Engineering in Juncos, PR seeks a Commissioning & Qualification Scientist/Engineer to lead validation activities in Bio/Pharmaceutical environments. You will generate and execute validation documents, develop qualification protocols, and prepare comprehensive reports.

Ideal candidates combine a engineering or life sciences background with hands-on CQ experience, strong collaboration skills, and fluent English and Spanish communication. This in-person role requires relocation to PR.