Aditi Consulting | Process Engineer
3 days ago
Job Title: Process Engineer
Location: Thousand Oaks, CA
Duration: 12 Months
100% Onsite Thousand oaks
Relocation: Position requires onsite presence, however candidates willing to relocate on their own are welcome to apply.
Ideal candidate: Experience as a process engineer or similar role in equipment ownership. Strong reliability background and independence in problem-solving
Capable of networking with other buildings and teams to implement reliability programs. Tools include Excel, JMP, and basic knowledge of Python (used by the software team)
Examples of solving equipment reliability problems are encouraged. Data analysis and problem-solving skills, Strong communication and collaboration abilities
Preferred industries: Pharmaceutical, biotech, or medical devices. Open to candidates from other industries with strong reliability backgrounds (e.g., aerospace). GMP experience: Not mandatory, but experience in regulated environments is beneficial
Bachelor Engineering process mechanical degree and 5 years of experience
This engineering position supports manufacturing activities associated with cGMP equipment and facilities at *** Thousand Oaks (ATO). The senior engineer works in partnership with the automation, maintenance, and manufacturing teams to develop and oversee the reliability of equipment while driving safety and quality compliance. The engineer will provide data to support business cases and long term strategy.
The Senior Engineer role will provide direct engineering technical support as follows:
• Demonstrating role modeling of leadership behaviors and positive values to create a positive working environment.
• Be accountable for manufacturing equipment reliability
• Suggest design modifications to address risks and design in quality and safety.
• Ensure that work executed with safety compliant practices and documented in accordance with cGMP good documentation
Top 3 Must Have Skill Sets:
• Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation
• Direct knowledge of design and troubles hooting with GMP Biopharmaceutical Production facility equipment/systems such as cell culture reactors, chromatography, filtration, filling, lyophilization, inspection, device assembly, as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.
• Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.)
Day to Day Responsibilities:
• Identify, support, and/or lead implementation of engineering based improvements or upgrades to the equipment or facility systems. This may include development of business case for improvement and identification of design requirements and then translation of requirements into process equipment/system design, specification and supporting the construction, startup, and validation of equipment.
• Directing and coordinating equipment maintenance as necessary to ensure systems are in proper working order
• Monitor systems to identify performance risks and implement risk reduction strategies
• Providing trouble shooting support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis and implementation of corrective/preventive action
Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions.
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