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Associate Controls Engineer Jobs in Riverside, CA

Senior Machine Learning Engineer

Irvine, CA · On-site

$111K - $153K/yr

We believe that belonging leads to better outcomes and a stronger community of associates united by ... You embed data lineage, access controls, audit trails, and responsible AI practices into every ...

... Associate's degree with a focus in Electronic Technology (or similar) • Bachelor's degree in a ... advanced automation controls systems maintenance and development • 3+ years of experience ...

... Associate's degree with a focus in Electronic Technology (or similar) • Bachelor's degree in a ... advanced automation controls systems maintenance and development • 3+ years of experience ...

Hotel Engineer

Anaheim, CA · On-site

$28.65/hr

We also support our associates with free parking and complimentary hot buffet meals during breaks ... air conditioning controls, television sets, lighting systems, and make minor repairs and/or ...

We also support our associates with free parking and complimentary hot buffet meals during breaks ... air conditioning controls, television sets, lighting systems, and make minor repairs and/or ...

Overnight Engineer

Anaheim, CA · On-site

$28.65/hr

We also support our associates with free parking and complimentary hot buffet meals during breaks ... air conditioning controls, television sets, lighting systems, and make minor repairs and/or ...

Overnight Engineer

Anaheim, CA · On-site

$28.65/hr

We also support our associates with free parking and complimentary hot buffet meals during breaks ... air conditioning controls, television sets, lighting systems, and make minor repairs and/or ...

Software Programmer

Orange, CA · On-site

$35 - $42/hr

Associate Employment Type: Full-time Compensation: This hourly, non-exempt position pays from $35 ... tools, or controls; reach with their hands and arms; and communicate verbally. The employee ...

... controls, programming settings, manufacturing equipment, metal detection, and varied fields of ... An Associates or higher degree, vocational education, apprenticeship program, certificates or ...

... controls, programming settings, manufacturing equipment, metal detection, and varied fields of ... An Associates or higher degree, vocational education, apprenticeship program, certificates or ...

CNC Programmer/Operator

Corona, CA · On-site

$20 - $22/hr

High School Diploma (Associates Preferred) * Able to work 40 hours a week * This position reports ... Controls and Instrumentation, Equipment Maintenance, Manufacturing Experience, Manufacturing ...

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Showing results 1-20

Associate Controls Engineer information

See Riverside, CA salary details

$57.4K

$100.8K

$136.7K

How much do associate controls engineer jobs pay per year?

As of Jun 18, 2026, the average yearly pay for associate controls engineer in Riverside, CA is $100,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,100.00 and $112,700.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Associate Controls Engineers when working on multidisciplinary teams?

Associate Controls Engineers often collaborate with professionals from mechanical, electrical, and software engineering backgrounds. One common challenge is ensuring clear communication across disciplines, as each team may use different technical jargon and have distinct priorities. Additionally, balancing project timelines while integrating control systems with hardware and software components can require strong organizational and problem-solving skills. Proactively seeking feedback and participating in cross-functional meetings can help Associate Controls Engineers bridge gaps and contribute effectively to project success.

What are the key skills and qualifications needed to thrive as an Associate Controls Engineer, and why are they important?

To thrive as an Associate Controls Engineer, you need a solid background in electrical engineering, control systems, and automation, often supported by a relevant bachelor's degree. Familiarity with PLC programming, SCADA systems, and industry-standard software such as AutoCAD or Rockwell Automation tools is typically required. Strong problem-solving, analytical thinking, and effective communication skills help you collaborate with cross-functional teams and resolve technical challenges. These competencies are crucial for designing efficient control solutions, ensuring system reliability, and driving project success in automated environments.

What does an Associate Controls Engineer do?

An Associate Controls Engineer assists in designing, developing, and maintaining control systems used in manufacturing or industrial settings. They work with senior engineers to implement automation solutions, troubleshoot issues, and ensure equipment operates safely and efficiently. Their tasks often include programming controllers, testing system performance, and supporting the integration of new technologies. This role typically requires knowledge of electrical engineering, programming languages like PLC, and a strong attention to detail.

What is the difference between Associate Controls Engineer vs Controls Engineer?

AspectAssociate Controls EngineerControls Engineer
Required CredentialsBachelor's in Electrical, Mechanical, or Automation Engineering; some certificationsBachelor's or higher in related engineering; often more experience or certifications
Work EnvironmentEntry-level, supporting design, testing, and troubleshootingMore independent, leading projects, and system integration
Employer & Industry UsageManufacturing, automation, and industrial facilitiesSimilar industries, with increased responsibilities

The main difference between an Associate Controls Engineer and a Controls Engineer lies in experience and responsibility level. Associate Controls Engineers typically support and assist in projects, focusing on learning and executing tasks under supervision. Controls Engineers take on more independent roles, managing projects and system design. Both roles require similar educational backgrounds and certifications, but Controls Engineers usually have more hands-on experience and leadership responsibilities.

What are the most commonly searched types of Controls Engineer jobs in Riverside, CA? The most popular types of Controls Engineer jobs in Riverside, CA are:
What are popular job titles related to Associate Controls Engineer jobs in Riverside, CA? For Associate Controls Engineer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Associate Controls Engineer jobs in Riverside, CA look for? The top searched job categories for Associate Controls Engineer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Associate Controls Engineer jobs? Cities near Riverside, CA with the most Associate Controls Engineer job openings:
Infographic showing various Associate Controls Engineer job openings in Riverside, CA as of June 2026, with employment types broken down into 1% As Needed, 45% Full Time, 53% Part Time, and 1% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $100,752 per year, or $48.4 per hour.
Associate Director, Labeling & Technical Writer

Associate Director, Labeling & Technical Writer

Becton, Dickinson and Company

Irvine, CA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 19 days ago


BD rating

7.2

Company rating: 7.2 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

268th of 418 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Associate Director, Senior Technical Writer

Job Summary:

This role is a strategic operations leader responsible for transforming and scaling the technical documentation and labeling function.The Associate Director will drive end-to-end process redesign, standardization, and automation across documentation and labeling workflows to improve cycle time, quality, and compliance.The Associate Director, Senior TechnicalWriteris a strategicand results-orienteddocumentation leader responsible fordesigning anddriving the development, quality, and evolution of technical documentation for Class II medical devices. This role combines deepexpertisein technical writing with strong people leadership,process design,crossfunctionalinfluence, and operational excellence,and continuous improvement.This leader owns the operating model for documentation-establishinggovernance, metrics, and tooling that enable predictable, high-quality delivery in a regulated environment while partnering cross-functionally to integrate documentation seamlessly into product development.

Key Responsibilities:

Leadership & Team Management

  • Lead, develop, and mentor a team of technical writers, illustrators, and/or documentation specialists; provide coaching, performance feedback, and career development.

  • Oversee the labeling function, ensuring packaging and IFU content processes are standardized, compliant, and integrated with regulatory and manufacturing workflows

  • Design and build ahighperforming, best in classdocumentation function byestablishingclear expectations, aligning team goals to organizational priorities, and fostering a culture of quality, accountability, and continuous improvement.

  • Drive consistency and efficiency across labeling change control, translations, and global deployment.

  • Oversee resource planning, workload balancing, and vendor/contractor management as needed.

  • Represent the documentation function inexecutiveleadership forums andownfunctional updates whileinfluencingdecisions affecting product development, quality, labeling, and regulatory deliverables.

Documentation Strategy &Labeling Operations / Process Excellence

  • Own and standardize the end-to-end documentation and labeling lifecycle, ensuring seamless integration with product development, design controls, and regulatory submission workflows.

  • Have deep rooted knowledgeinindustrystandards and ensure compliance with FDA, EU MDR, ISO 13485, and other relevant standards; embed regulatory and quality requirements into documentation workflows.

  • Establish scalable, standardized frameworks for content creation, review, and approval to enable content reuse, reduce variability, and support global regulatory needs.

  • Implement quality systems and upstream controls to drive "right-first-time" documentation and reduce downstream review cycles.

CrossFunctionalInfluence & Collaboration

  • Partner with engineering, quality assurance, regulatory affairs, clinical/medical affairs, marketing, customer support, and global business units to gather information,validatecontent, and align documentation with product requirements.

  • Serve as the documentation authority incrossfunctionalmeetings, influencing project scope, timelines, and risk mitigation strategies.

  • Communicate effectivelyand confidentlywith senior-level stakeholders and international partners, ensuring alignment andtimelydelivery of all documentation commitments.

Content Creation & Technical Expertise

  • Create and edit technical documents with a high degree of accuracy, clarity, and regulatory compliance.Foster a team with the same sense of rigor in their review standards.

  • Developmodernvisual content including diagrams, illustrations, flow charts, line art, and product photography; advise engineering teams on data visualization and content usability.

  • Stay current on industry trends, regulatory developments, and advancements in technical communication tools and methodologies.

Program & Project Management

  • Manage documentation schedules, dependencies, resource requirements, and deliverables within fast-paced project environments.Utilize data-driven metrics to drive program decisions and timelines.

  • Revampthe functional team to drive process improvements to increase efficiency, reduce cycle times, and enhance documentation quality.

  • Oversee version control, change management, and documentation integration within enterprise systems.

Required Qualifications

  • Bachelor's degree in Technical Communication, Engineering, or a related technical or communications field required.

  • 7+ years of experience in technical writing, technical communication, or documentation development required.

  • 5+ years of experience within a regulated industry (medical devices strongly preferred; pharma/biotech acceptable).

  • 3+ years of people leadership experience, including managing writers, contractors, or crossfunctional documentation teams required.

Preferred Qualifications

  • Master's degree in Technical Communication, Regulatory Science, Engineering, Biomedical Engineering, Life Sciences, or a related discipline

  • Prior leadership of technical writing teams within a medical device organization.

  • Extensive experience in regulated industries such as medical devices or pharmaceuticals, with deep knowledge of regulatory compliance and documentation requirements.

  • Demonstrated leadership experience managing teams or cross-functional documentation programs.

  • Strong collaboration skills working with engineering, marketing, clinical, quality, and regulatory teams.

  • Proven ability to manage multiple complex projects under tight deadlines.

  • Strong initiative, problemsolving skills, and ability to work independently with minimal supervision.

  • Familiarity with electro-mechanical systems and software applications.

  • Experience with device labeling and packaging content.

  • Knowledge of engineering change control processes and Agile methodologies.

  • Experience with ERP systems such as SAP or Oracle.

  • Proficiency with version control systems (Perforce, Subversion, TFS, GitHub).

  • Skilled in technical editing tools (Microsoft Word, Acrobat, editorial symbols).

  • Proficiency with DTP tools (MadCap Flare, Adobe FrameMaker, InDesign, Illustrator, XML, DITA).

  • Experience with photography and image editing (Adobe Photoshop).

  • Experience working with global regulatory submissions and countryspecific documentation requirements.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

At BD, we are committed to supporting our associates' well-being, development, and success through a performance-based culture. For this position, BD offers a competitive compensation package along with the following benefits specific to this role:

  • Annual Bonus

Health and Well-being Benefits

Medical coverage, Health Savings Accounts, Flexible Spending Accounts, Dental coverage, Vision coverage, Hospital Care Insurance, Critical Illness Insurance, Accidental Injury Insurance, Life and AD&D insurance, Short-term disability coverage, Long-term disability insurance, Long-term care with life insurance.

Other Well-being Resources

Anxiety management program, wellness incentives, sleep improvement program, diabetes management program, virtual physical therapy, emotional/mental health support programs, weight management programs, gastrointestinal health program, substance use management program, musculoskeletal surgery, cancer treatment, and bariatric surgery benefit.

Retirement and Financial Well-being

BD 401(k) Plan, BD Deferred Compensation and Restoration Plan, 529 College Savings Plan, financial counseling, Baxter Credit Union (BCU), Daily Pay, college financialaidand application guidance.

Life Balance Programs

Paid time off (PTO), including all required State leaves, educational assistance/tuition reimbursement, MetLife Legal Plan, group auto and home insurance, pet insurance, commuter benefits, discounts on products and services, Academic Achievement Scholarship, Service Recognition Awards, employer matching donation, workplace accommodations.

Other Life Balance Programs

Adoptionassistance, backup day care and eldercare, support for neurodivergent adults, children, and caregivers, caregivingassistancefor elderly and special needs individuals, Employee Assistance Program (EAP), paid parental leave, support for fertility, birthing, postpartum, and age-related hormonal changes.

Leave Programs

Bereavement leaves, Military leave, Personal leave, Family and Medical Leave (FML),Juryand Witness Duty Leave.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work LocationUSA CA - San Diego Bldg A&BAdditional LocationsUSA CA - Irvine Laguna Canyon, USA NJ - Franklin LakesWork Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$169,800.00 - $280,300.00 USD Annual

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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