Atrium · 7 hours ago
Senior Controls Engineer (Contract)
Atrium is seeking a Senior Controls Engineer to revolutionize Cell & Gene Therapy. In this role, you will be responsible for designing control and automation systems to enhance manufacturing reliability and streamline processes within the biotechnology field.
Real Estate
Responsibilities
Design control and automation systems from benchtop to commercial across multiple therapeutic modalities. Perform tuning and troubleshooting of control loops, hardware, and software. This will include integrating multiple components and technologies, such as PLCS, relays, valves, MFCs, HMIs, actuators, robotics, and sensors
Programming software, including, but not limited to Ladder Logic, Functional Block Diagram, Structured Text, Sequential Function Charts, and Instruction List. Programming environments include, but are not limited to Rs Logix, TIA Portal, Delta V Programming Environment, B&R Automation Studio, and various robotic programming environments
Design equipment to interface with enterprise level systems, including, but not limited to, Oracle OPM, POMS MES, Ignition SCADA, OSI PI Historian, and Sepasoft Batch management
Design and manage external design of electrical schematics, industrial control panels, and P&IDs
Co-create Machine Safety Risk Assessments. Design equipment and engineering safeguards that meet applicable laws, regulations, and standards
Support FAT, SAT, commissioning, and qualification activities
Provide periodic status updates to Project Management and cross-functional partners
Create phase plans for automation systems and contribute to an automation masterplan
Create and oversee the creation of technical documentation, including, but not limited to URS, FRS, FMEAs, P&IDs, manuals, work instructions, and maintenance plans
Execute assigned duties on time and within budget; proactively communicate delays and other issues to relevant stakeholders
Comply with all regulatory, corporate, and Quality System policies. Support Deviation Management, CAPA, and Change Control activities, as required
Performs other duties as assigned
Qualification
Required
BS or MS in engineering or another relevant discipline
10+ years of experience working within an electrical and controls environment (pharmaceutical, cGxP preferred). Experience with cell & gene therapy is highly desirable
Experience working with Delta V, Allen Bradley, and Siemens
Knowledge and practical experience of Equipment related laws, regulations, and standards
Understanding of cGxP principles and practices and familiarization with ISO 13485, ISO 14971, and 21CFR820 is a plus. Knowledge of global cGMP requirements governing device or combination products
Experience troubleshooting industrial automation, including, but not limited to PLCs, camera systems, and sensors
Must be able to work independently with adequate supervision, multi-task, and support several projects simultaneously
Sense of urgency, ability to act/escalate promptly, and transparently communicate issues to involved stakeholders and management
Must demonstrate strong interpersonal, presentation, and teamwork skills
Benefits
Compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer.
This role will be eligible for overtime pay, in accordance with federal and state requirements
Company
Atrium
Atrium is a global WBENC-certified Talent Solutions and Extended Workforce Management leader.
H1B Sponsorship
Atrium has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2021 (2)
2020 (4)
Funding
Current Stage
Growth StageLeadership Team
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