Process Engineering Positions

Temp to hire potential 8am-5pm Hybrid - 3 days on-site, 2 days remote
Required Skills

Biological License Application (BLA) fi ling experience with the FDA/regulatory agencies
Commercial manufacturing experience
Validation activities management
Preferred Skills

Process development or manufacturing experience
Chemistry background
Process development and manufacturing expertise are high-value additions
Summary
The Carlsbad Gene Therapy Viral Vector Manufacturing facility is a contract manufacturing site that produces drug substances and drug products for gene therapy and oncology applications. We are seeking a Process Validation Engineer who will be responsible for developing, reviewing, and managing the execution of validation activities. In this role, you will provide technical leadership within cross-functional teams with primary responsibility as subject matter expert in the strategy for process validation of unit operations within the Carlsbad viral vector manufacturing facilities (CLD‑VVM). As part of a dynamic Contract Manufacturing Organization, the successful candidate will work cross-functionally with the Manufacturing, Process and Analytical Development, Quality Control, Quality Assurance, and Project Management teams to ensure successful implementation and coordination of process validation activities.
Responsibilities

Write risk assessments to assess and identify potential risks associated with various manufacturing processes and facility activities.
Assisting in creating process documentation to ensure production processing consistent within validated parameters.
Monitor event trends to provide proactive corrections/improvement alternatives to minimize the potential for repeat incidents.
Acts as a technical liaison, as needed, between process development, manufacturing, external manufacturers and suppliers.
Capable of singular project management (within the realm of validation Engineering) for smaller scope validation engineering plans.
Evaluate equipment or process problems and design testing to determine possible causes or solutions.
Assist in determining process capability of new equipment.
Assists in ensuring process development activities have all necessary validation support.
The Validation Engineer is responsible for the design, schedule, execution, and evaluation of scientifically and statistically sound Qualification/Validation experiments which define and demonstrate that critical Cleaning, Controls, Equipment, Facilities, Processes and Utilities function in a consistent and repeatable manner, and are in compliance with regulatory requirements, product license restrictions, and policies affecting final product integrity.
Define and implement process validation framework
Implement consistent process qualification, process validation and continuous process verification (CPV) strategies
Define strategy for execution of process performance qualification (PPQ) and product life cycle
Generate, review, and approve process validation protocols and reports
Lead development of studies around process hold time, homogeneity, mixing etc
Lead establishment of drug substance/API manufacturing process control strategies and assess process performance by monitoring and analyzing process/product data
Lead process validation related investigations
Work closely with the client and personnel from Manufacturing, Process Development, Quality Control, Quality Assurance, Operations, and Project Management to ensure the scientific and CMC strategies are robust and maintained.
Data Management, Generation of Process Validation/CPV documents.
Organizes, manages and interprets data, performs detailed data analysis.
Execute complex validation impact assessments with robust rationale
Process Validation SME in audits and customer meetings
Manage escalation within MSAT, customer and Project Team as it relates to job function and deliverables
Self starter with ability to manage work load with minimal supervision
Ability to drive sound decision making
Ability to drive project forward with collaboration
Comfortable in a fast-paced environment with the ability to adjust to changing priorities
Minimum Qualifications

• Minimum of 7+ years experience in cGMP environment
• Bachelor s or Master s degree Biochemistry, Chemistry, Chemical Engineering, Microbiology, or other Life Science related field
• 5+ years experience with process validation, Process Performance Qualification (PPQ) and / or Continued Process Verification (CPV)

• 10+ years experience / subject matter expert (SME) level of understanding with manufacturing, process validation, Process Performance Qualification (PPQ), and Continued Process Verification (CPV)
• 5+ years of hands on experience working directly with cell culture upstream operations (flask expansion, cell stacks, bioreactors, clarification), or downstream purification (TFF (UF/DF), automated chromatography skids (AKTA, XMO), and/or sterile filtration)
• Ability to lead and influence teams/efforts and processes without direct authority
• Critical thinking skills that translate into improved outcomes/outputs, and ability to effectively solve and derisk technical problems and form solutions/plans to mitigate issues
• Familiarity with cGMP document control systems and general procedures
• Excellent attention to detail, with superior documentation and organization skills
• Excellent computer, verbal, and written communication skills, including strong technical writing ability and a demonstrated ability to communicate scientific ideas to a broader cross-functional (technical/non-technical) audience