Cell Therapy GMP Validation Engineer

Cellipont Bioservices; The Woodlands (TX); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Career growth opportunities

401K strong employer match

Tuition Reimbursement

Flexible work schedules

Paid holidays

Job summary

Cellipont Bioservices is seeking a Validation Engineer to support our validation initiatives. This role involves working on projects of medium complexity and will contribute to the validation lifecycle documentation for GMP use.

The ideal candidate has a solid understanding of cGMPs, strong problem-solving skills and the ability to thrive in a fast-paced environment. Opportunities for career growth and a robust benefits package are included.

Qualifications

• 1+ years of cGMP experience in the Pharmaceutical or Life Sciences industry.
• Ability to work independently with minimal supervision.
• Strong written and verbal communication skills.

Responsibilities

• Support GMP validation projects of low to medium complexity.
• Develop qualification and validation protocols and reports.
• Review validation lifecycle documentation.

Skills

cGMP understanding

Creative problem solving

Microsoft Office Suite

Interpersonal skills

Multi-tasking

Education

Bachelor's Degree in relevant field

Job description

Cellipont Bioservices is seeking a Validation Engineer to support our validation initiatives. This role involves working on projects of medium complexity and will contribute to the validation lifecycle documentation for GMP use.

The ideal candidate has a solid understanding of cGMPs, strong problem-solving skills and the ability to thrive in a fast-paced environment. Opportunities for career growth and a robust benefits package are included.