Manufacturing Sciences and Technology (MSAT) Process Engineer (3rd Shift)

Ring Inc; Princeton (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Annual bonus

Medical, dental, and vision coverage

PTO

401(k) plan

Life and AD&D insurance

Parental leave

Pre-IPO equity

Job summary

Ring Inc is seeking a MSAT Process Engineer to improve the efficiency and safety of drug product manufacturing. You will manage lifecycle activities for clinical and commercial products, monitor processes, and drive improvements with validation and change control execution.

Responsibilities include monitoring, reporting, investigations, CAPA, and supporting validation protocols, change controls, and testing within lifecycle management.

Qualifications

• B.S. in Engineering or similar field.
• 3+ years in manufacturing processes and equipment.
• Experience in regulated GMP manufacturing operations.
• Biotechnology and cell therapy experience preferred.
• Strong communication and problem solving skills.
• Flexibility to work outside standard hours when needed.

Responsibilities

• Monitors existing products and processes.
• Generates metrics and reports for process monitoring and continuous verification.
• Supports process improvements and changes including electronic batch records.
• Investigates process events and implements CAPA.
• Provides troubleshooting for manufacturing events, equipment, and materials.
• Performs root cause analysis and determines corrective actions.
• Owns change controls, protocols, reports, and lifecycle activities.
• Writes and validates testing protocols in line with lifecycle management.

Skills

Strong communication

Problem solving

Shift flexibility

GMP experience

Education

B.S. in Engineering or related field

Job description

The MSAT Process Engineer works to improve the efficiency and safety of the drug product manufacturing process. This role is responsible for lifecycle management of clinical and commercial products including process monitoring and troubleshooting, implementation and validation of process improvements and changes, and supporting investigations and corrective/preventive actions.

Essential Duties & Key Responsibilities

• Performs ongoing monitoring of existing products and processes
• Generate metrics and reports for process monitoring and continuous process verification
• Support process improvements and changes including electronic batch record creation and modifications
• Investigates process events and implements corrective and preventive actions
• Provides troubleshooting support for manufacturing events, equipment performance and material issues
• Performs root cause analysis to isolate cause of events and determine appropriate corrective actions
• Authors, executes and owns change controls, technical protocols, reports and activities to support improvements
• Writes and ensures proper execution of validation protocols and testing in line with required lifecycle management activities

Minimum Qualifications

• B.S. in Engineering or similar fields
• 3+ years of experience with manufacturing processes and equipment in related fields: biologics, pharmaceutical fill and finish or drug substance manufacturing, chemical or food industries
• Prior experience in regulated, GMP manufacturing operations
• Experience in biotechnology and cell therapy manufacturing preferred
• Strong communication and problem solving skills, with a desire to improve upon established processes
• Flexibility to work outside standard business hours when needed to support site priorities, deadlines, or critical business needs.

2nd Shift

• Monday - Friday, 4:00pm - 12:30am

3rd Shift

• Monday - Friday, 12:00am - 8:30am

Physical Demands

• Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment.
• Most roles must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.

$80,000 - $100,000 a year

The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. Full-time employment positions will also be eligible to receive pre-IPO equity and annual bonus, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits.