Avid Bioservices, Inc.

Automation Engineer

Avid Bioservices, Inc.$101K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in electrical engineering, Automation Technology, or related field
  • 5+ years of experience in an FDA/cGMP regulated environment
  • Familiarity with DDC, DCS, PLCs, and industrial automation components
  • Experience with process instrumentation and Air Handler HVAC systems
  • Proven ability to troubleshoot systems independently
  • Good technical writing skills with strong attention to detail
  • Proficient in basic MS Office applications

Responsibilities

  • Collaborate with teams to enhance production effectiveness and reduce costs
  • Advance products from clinical stages to commercial launch
  • Focus on continuous process improvement following FDA standards
  • Maintain and troubleshoot control systems and instrumentation
  • Track and analyze critical process data for improvements
  • Develop and maintain electrical and P&ID drawings
  • Support validation and manufacturing projects

Benefits

  • Comprehensive health, dental, and vision insurance
  • 401(k) matching program
  • Opportunities for career growth and development
  • Supportive and inclusive work environment
  • Paid time off and potential for performance-based bonuses
Full Job Description
Description

Your Role:

Join the Avid team as an Automation Controls Engineer and help us improve patient lives and support innovative therapies worldwide. As our 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.

Key Responsibilities:
  • Collaborating with operations, quality assurance, vendors, and suppliers to maximize production effectiveness and optimize performance while lowering operating costs.
  • Advancing products from clinical development to commercial launch
  • Focusing on continuous process improvement and documentation according to FDA standards
  • Maintaining control systems, performing maintenance, troubleshooting, and conducting root cause analyses
  • Tracking and evaluating critical process data to recommend process improvement.
  • Developing and maintaining electrical and P&ID drawings
  • Supporting validation and manufacturing projects
  • Maintaining knowledge of regulatory and industry standards
  • Participating in inspections/audits and providing written responses as necessary
  • Adhering to FDA regulations, corporate safety policies, and other assigned tasks.
  • Other tasks as assigned.

Minimum Qualifications:
  • Bachelor's degree in electrical engineering, Automation Technology, or related technical discipline
  • 5+ 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
  • Good 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 in our Costa Mesa, CA location. Days and hours of work are Monday through Friday, 7:00am to 4:00pm PST unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.

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 $101,600 to $120,000 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 25 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.

About Avid Bioservices, Inc.

Avid Bioservices, Inc. is a contract development and manufacturing organization (CDMO) focused on development and CGMP manufacturing of biopharmaceutical drug substances derived from mammalian cell culture. The company provides a comprehensive range of process development, high quality CGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. With 25 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and perfusion modes, Avid's services include CGMP clinical and commercial drug substance manufacturing, bulk packaging, release and stability testing and regulatory submissions support. The company also provides a variety of process development activities, including cell line development and optimization, cell culture and feed optimization, analytical methods development and product characterization.
Learn more about Avid Bioservices, Inc.
Size
321 employees
Market Cap
$873.5 million
Industry
Net Income
$4.4 million
5 Year Trend
+15.7%
Revenue
$80.8 million
NASDAQ

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