Sr. Automation Controls Engineer

Posted 8 Hours Ago
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Tustin, CA, USA
In-Office
122K-152K Annually
Senior level
Healthtech • Pharmaceutical
Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Maintain, troubleshoot, and improve automation control systems supporting biopharmaceutical manufacturing processes and utilities. Responsibilities include root cause analysis, process data evaluation, electrical and P&ID documentation, validation and manufacturing project support, regulatory compliance, audits, and equipment installations or upgrades. The role collaborates with operations, quality, vendors, and suppliers, requires strong technical writing and prioritization skills, and includes full-time onsite work with on-call, weekend, holiday, and extended-hours support.
Summary Generated by Built In
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
 
Your Role:    
As our Sr. Automation Controls Engineer, you'll be responsible for ensuring that our manufacturing processes and utilities are in tip-top shape and running like a dream. Whether it's maintaining control systems, identifying potential issues, or participating in installations and upgrades, you'll be the one leading the charge.   
  • Collaborate with operations, quality assurance, vendors, and suppliers to maximize production effectiveness and optimize performance while lowering operating costs.
  • Advance products from clinical development to commercial launch.
  • Focus on continuous process improvement and documentation according to FDA standards.
  • Maintain control systems, perform maintenance, troubleshoot, and conduct root cause analyses.
  • Track and evaluate critical process data to recommend process improvement.
  • Develop and maintain electrical and P&ID drawings.
  • Support validation and manufacturing projects.
  • Maintain knowledge of regulatory and industry standards.
  • Participate in inspections/audits and provide written responses as necessary.
  • Adhere to FDA regulations, corporate safety policies, and other assigned tasks.
  • Other tasks as assigned.
  • Other duties may be assigned.
Minimum Qualifications:
  • Bachelor's degree in electrical engineering, automation technology, or a related technical field. Alternatively, five or more years of relevant experience coupled with an Associate's degree, or ten or more years of experience with documented automation training from a certified software or hardware vendor, will be considered.
  • 8+ years of experience in an FDA/cGMP regulated environment.
  • Experience with DDC, DCS, PLCs, industrial networks, drives, motor controls, sensors, automation components, control instrumentation, proportional valves, servo controls, SCADA, and HMI troubleshooting is preferred.
  • Familiarity with various types of process instrumentation and Air Handler HVAC systems.
  • Understanding of good programming standards and practices.
  • Proven ability to independently learn and troubleshoot systems and devices.
  • Familiarity with common codes and standards, electrical circuits, and Virtual Servers/Windows Server.
  • Strong technical writing skills.
  • Strong attention to detail and work ethic.
  • Ability to prioritize and manage multiple tasks to meet deadlines.
  • Strong interpersonal skills to work effectively in a team environment.
  • Proficiency in basic MS Office (Outlook, Word, and Excel)
Position Type/Expected Hours of Work:  
This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. Must be available to work holidays, weekends, or extended hours if needed. This position includes participation in an on-call rotation to provide support outside of regular business hours.
 
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
 
The compensation range for this role is $121,600 - $152,000 annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.   
   
Who you are:   
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:   
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position. 

Skills Required

  • Bachelor's degree in electrical engineering, automation technology, or a related technical field
  • Alternatively, five or more years of relevant experience with an Associate's degree
  • Alternatively, ten or more years of experience with documented automation training from a certified software or hardware vendor
  • 8 or more years of experience in an FDA or cGMP regulated environment
  • Experience with DDC, DCS, PLCs, industrial networks, drives, motor controls, sensors, automation components, control instrumentation, proportional valves, servo controls, SCADA, and HMI troubleshooting
  • Familiarity with process instrumentation and Air Handler HVAC systems
  • Understanding of good programming standards and practices
  • Ability to independently learn and troubleshoot systems and devices
  • Familiarity with common codes and standards, electrical circuits, and virtual servers or Windows Server
  • Strong technical writing skills
  • Strong attention to detail and work ethic
  • Ability to prioritize and manage multiple tasks to meet deadlines
  • Strong interpersonal skills for effective teamwork
  • Proficiency in Microsoft Outlook, Word, and Excel
  • Availability for holidays, weekends, extended hours, and on-call rotation

Avid Bioservices Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Avid Bioservices and has not been reviewed or approved by Avid Bioservices.

  • Healthcare Strength Health coverage includes medical, dental, and vision alongside life and disability insurance. Plan breadth is presented as solid, with health benefits frequently highlighted as a strong element of the package.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discounted purchase feature and the availability of stock grants provide accessible ownership opportunities. These components add long-term value beyond base pay.
  • Fair & Transparent Compensation Pay ranges are posted for some roles, offering upfront clarity on expected compensation. This transparency supports clearer expectations during hiring.

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The Company
HQ: Tustin, California
343 Employees
Year Founded: 2002

What We Do

Avid Bioservices is transforming the CDMO experience, with more than 30 years of unrivaled experience manufacturing biologics, and world-class mammalian protein facilities. We’ve produced more than 250 commercial batches, and 5 commercial products marketed in 90+ countries. For more than 10 years, we’ve maintained a flawless quality track record which we’re committed to uphold. We do it right the first time, which saves money and time. From early-stage to late-stage, concept to market, every part of our process is personalized. We’re your advocates, your trusted experts, your true partners.

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