Process Engineer I — GMP Lab & Validation

Bausch + Lomb; City of Rochester (NY); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401K Plan

Paid Time Off

Tuition Reimbursement

Employee Stock Purchase Plan

Performance Bonus

Job summary

Bausch + Lomb is seeking candidates to perform technical and supporting activities for Medical Device product manufacture in the Solutions Process Development Pilot Laboratory. The role includes validation, documentation, and support for sterile and non-sterile products.

You will contribute to process development, documentation, and compliance in a GMP environment, with opportunities for growth and thorough training.

Qualifications

• Bachelor's degree or the equivalent with 0-3 years of relevant experience.
• MS with 0-2 years of relevant experience.
• Experience in a GMP laboratory/facility environment.
• Knowledge of good documentation practices.

Responsibilities

• Performs and/ or supports validation activities and documents validation results.
• Supports compounding, filling, packaging and labeling of sterile and/or non-sterile products.
• Coordinates and oversees maintenance of department utilities and equipment.
• Monitors environmental monitoring data and calibration activities.
• Maintains department documentation and supports change control processes.

Skills

Organization

Attention to detail

Multitasking

Verbal communication

Written communication

Teamwork

Education

Bachelor's degree

MS

Job description

Bausch + Lomb is seeking candidates to perform technical and supporting activities for Medical Device product manufacture in the Solutions Process Development Pilot Laboratory. The role includes validation, documentation, and support for sterile and non-sterile products.

You will contribute to process development, documentation, and compliance in a GMP environment, with opportunities for growth and thorough training.