Automation Engineer V - SCADA - Greater Los Angeles
Compli

Job Info

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Automation Engineer V - SCADA - Los Angeles Surrounding Area

(Pharmaceutical/Biotech)-Competitive Salary, Work/Life Balance!

On-Site / Pay W-2

Previous Pharmaceutical/Biotech/Medical Device experience is mandatory for these roles.

Are you looking to be a part of a close-knit work community? Do you have experience in the Life Science industry? Will you represent Compli, LLC as an experienced Automation Engineer for our pharmaceutical manufacturing, biotech, and medical device client projects? Do you enjoy traveling the country and making a difference? If so, this could be the right opportunity for you!

Important: Our Client has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Compli' s client are required to comply with this requirement.

Responsibilities

• Perform automation and instrumentation and control engineering design services for existing facility projects, including upgrades and capacity expansions, equipment upgrading and replacement.
• Produce and review design drawings and specification documents (URS, FS, DS, etc.).
• Generate, execute, and review design testing, generate and participate in functional specification testing, and perform field inspection services.
• Generate, execute, and review Installation, Operational, and Performance Qualification protocols.
• Generate, review, and approve GMP Lifecycle Documents (e.g., risk documents, trace matrices, periodic review, etc.)
• Execute and track progress of change records.
• Manage personal project activities (design and qualification) following Genentech/Roche business processes to deliver results that are right first time, on-time with schedule requirements and reconciled to the budget.
• Troubleshooting of automation and critical process utility systems.
• Lead plant operations to assess discrepant events and changes for automation impact, deliver automation solutions to resolve operational issues, assist in troubleshooting and providing real time on floor support of manufacturing operations, participate in site coordination meetings and attend network meetings.
• Adhere to site SOPs and WIs for daily and project deliverables and provide improvements to business processes.
• Attendance and participation in department and staff meetings.
• Maintain training qualifications.
• Adhere to company policies regarding performance management, department time reporting and notification requirements, budget, and expense reporting guidelines.
• Track project deliverables and provide status updates to project team.
• All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA).
• Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one's functional area. Fosters a positive safety culture in which no one gets hurt.

Skills

• Experience with Biopharmaceutical manufacturing, design or/and construction.
• Knowledge of process, utility and building control systems.
• Knowledge of GMP guidelines, experience in generation of controlled documents.
• Qualification experience related to control and computer systems.
• Ability to generate engineering drawings and specifications.
• Knowledge of ISA standards and practices for instrumentation.
• Knowledge of PID control theories and techniques.
• Knowledge of programmable logic controllers, and associated programming languages (RS Logix Preferred).
• Practical knowledge of distributed control systems, and associated programming languages - ***Strong DeltaV Coding***
• Knowledge of computer aided manufacturing automation.
• Demonstrate good organizational and time utilization skills.
• Demonstrate good written and verbal communication skills.
• Ability to comply with cGMP requirements (gowning, documentation, and procedures) for performing work within the manufacturing facility.
• Demonstrate strong working knowledge of PC based programs and web-based systems.
• Ability to work most of the time independently with minimal direct supervision.
• Demonstrate good interpersonal skills with an ability to interact well with a variety of personalities, discipline skills and educational levels.

Education:

• Bachelor's or master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 5 years' experience, or master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 4 years' experience.
• Minimum of 8 years applicable automation and/or instrument and control system experience.
• Minimum of 5 years in the pharmaceutical/biotech industry/GMP experience.

Compli, LLC was founded in 2001 to provide commissioning, validation, and regulatory support services, CQV, asset management, reliability engineering, and staff augmentation services to the life sciences industry. We serve pharmaceutical companies across the U.S. Regarding regulations and compliance, it has never been more important to understand the documentation and quality assurance activities as they relate to vendors, engineering, construction, and contractors, which is why clients trust the Compli team.

Perks of the Job:

• Competitive Pay commensurate with experience
• Work / Life Balance
• Working with a small, close-knit team where you are valued as an individual
• A learning environment and continuous advancement opportunities

Feel overqualified? Feel underqualified? Apply anyway if this sounds like the fit you are looking for! We have flexibility in how we hire the role.

To learn more and APPLY NOW: http://www.ucompli.com/careers

Agencies, Compli welcomes your qualified candidates. Please email compli-opportunities@ucompli.com to establish a relationship with our firm.

We are an equal opportunity employer M/F/D/V

Job Keywords: United States, Laverne, CA, Los Angeles, CA, Los Angeles County and Surrounding Area, Oceanside, California, Automation Engineer, Technical Writing, CQV, qualification, DeltaV Coding, PID, ISA

This job has expired.