Engineer​/Sr. Engineer - Validation

Sr. Validation Engineer

Bionova is seeking a motivated and innovative Sr. Validation Engineer to serve in the Facilities and Engineering department. The Sr. Validation Engineer will take a hands-on approach to performing the commissioning and qualification of systems (facilities, utilities, equipment & analytical instruments), processes and/or automation systems and include tasks such as preparing and executing protocols, analyzing test results, and preparing summary reports.

As required, this person may also investigate and troubleshoot discrepancies/deviations, propose solutions and manage CAPAs and change control. As part of the F&E team, you will drive cross-functional decisions and influence decisions of user teams as we grow the organization and expand capabilities to meet project goals that ultimately improve patient outcomes.

Essential Duties and Responsibilities:

• Oversight of Commissioning, SAT, FAT for utility and process systems
• Creation of protocols for and oversight of Commissioning, SAT, FAT for systems
• Creation and execution for development and/or qualification protocols (IQ, OQ, PQ) and summary reports, including data analysis
• Retrieve and compile data from electronic sources/databases and paper records
• Participate in execution of development and/or qualification studies
• Adheres to established regulations and follows cGxP established by site
• Assist in writing and revising other documentation including:
  Standard Operating Procedures (SOP), User Requirements Specifications (URS), System Impact Assessments (SIA), Validation Master Plan (VMP), Validation Project Plans (VPP), etc…
• Understanding of GxP documentation and technical writing abilities
• As required, in regulatory submissions and represents qualification during inspections from regulatory agencies and client audits
• As needed, sustains process equipment after construction.
• Executes (e.g. continuous improvement or NPI) changes to process equipment under QA oversight (GMP compliance)
• Follows GxP principles in troubleshooting equipment issues and ensures equipment is satisfying user (operations) requirements
• Operates within GMP quality systems as record owner or subject matter expert including deviations, change control, CAPA, audits and other quality systems.
• Assist in GMP compliant detailed design for facility under quality change management and for construction satisfying design intent
• Sustains systems after construction. Executes (e.g. continuous improvement or NPI) changes to systems under QA oversight (GMP compliance)
• Follows GxP principles in troubleshooting equipment issues and ensures equipment is satisfying user (operations) requirements
• Other activities and duties as required or assigned.

Working Conditions:

This position requires work in office, manufacturing, warehouse, and lab settings. The role requires walking, standing, stooping, kneeling, and crouching. The employee may occasionally lift and or move up to 40 pounds independently.

Qualifications:

• 5-10 years' experience performing duties of Process, Utilities, or Facilities Engineer with at least 3-5 years in a GMP manufacturing environment.
• Bachelor's of Science degree in engineering or related science discipline
• Excellent English verbal and written communication skills
• Experience using CMMS systems in cGMP facilities
• Strong technical knowledge of validation principles, Quality Systems, manufacturing, and facility equipment/systems
• Experience with systems for autoclaves, controlled temperature units, utilities (e.g., WFI, CDA, HVAC), single use bioreactors (SUB), mixers, warehouse, and/or QC instruments (e.g., HPLC, UPLCs)
• Knowledge of current GMP Standards
• Ability to work individually and in a team environment
• Ability to multitask and prioritize tasks
• Interact well and professionally with diverse group of individuals
• Self-motivated and willing to be proactive in resolving issues
• Flexibility with work hours to meet business needs, including weekends and holidays, as needed
• Experience with Master Control a plus
• Experience interacting with regulatory agencies to defend Quality Systems
• Comfortable in a fast-paced, collaborative small-company environment, working with minimal direction and able to adjust workload based upon changing priorities.

Compensation Range:
The base compensation range for this role is between $85,000 and $120,000. However, the actual compensation may vary depending on your experience and qualifications.

Health Benefits and Program:
Bionova offers health benefits at a subsidized rate.

Healthcare, Dental, and Vision insurance

Life Insurance and Disability Program: 100% covered by Bionova.

Retirement Plan (401K) Up to 8% of Employer Match

Paid time off up to two weeks

10 days of Holidays and 5 days of Sick Leave.

As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.