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Control Operator Jobs in Linden, NJ (NOW HIRING)

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs). This role supports the day-to-day operations within the Quality Control ...

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs). This role supports the day-to-day operations within the Quality Control ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs). This role supports the day-to-day operations within the Quality Control ...

Kashiv Biosciences LLC

QC Analyst III

Piscataway, NJ · On-site

$103K/yr

... standard operating procedures, standard test methods, validation protocols and reports. Salary ... CCRs according to the change control process; as well as providing analytical support for ...

Kashiv BioSciences, LLC

QC Analyst III

Piscataway, NJ · On-site

$103K/yr

Description QC Analyst III (Piscataway, NJ): Be primarily responsible for the execution and review ... standard operating procedures, standard test methods, validation protocols and reports. Salary ...

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Control Operator information

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$12

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$39

How much do control operator jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for control operator in Linden, NJ is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $20.10 and $28.80 per hour, depending on experience, location, and employer.

What is a control operator?

Control Operators are professionals responsible for monitoring and managing the operations of complex systems, such as machinery, power plants, or manufacturing processes. They ensure that systems run efficiently and safely by observing instruments, making necessary adjustments, and responding to alarms or system irregularities. Control Operators play a crucial role in maintaining optimal performance and preventing malfunctions by following established procedures and safety protocols. Their work often involves collaboration with other technical staff to troubleshoot and resolve issues quickly.

What skills and qualifications are needed to be a control operator?

To thrive as a Control Operator, you need a solid understanding of process control systems, mechanical or electrical troubleshooting, and generally a relevant technical diploma or degree. Familiarity with SCADA systems, programmable logic controllers (PLCs), and safety protocols is typically required, along with any necessary industry certifications. Strong attention to detail, problem-solving abilities, and effective communication skills help operators respond quickly and accurately to system changes or emergencies. These skills are crucial for maintaining safe, efficient, and reliable operations in industrial or utility environments.

What challenges do control operators face and how can they be managed?

Control Operators often work in fast-paced environments where quick decision-making and attention to detail are critical. Common challenges include managing multiple systems simultaneously, responding to alarms or unexpected events, and maintaining clear communication with team members across shifts. Effective management of these challenges involves thorough training, strong situational awareness, and adherence to established protocols. Regular team briefings and ongoing skills development also help ensure operational safety and efficiency.

What is the difference between Control Operator vs Control Room Operator?

AspectControl OperatorControl Room Operator
CredentialsTypically requires technical certifications or training in control systemsSimilar certifications, often with additional safety or industry-specific licenses
Work EnvironmentIndustrial plants, power stations, manufacturing facilitiesControl rooms within industrial or utility facilities
Industry UsageCommon in energy, manufacturing, and utilitiesPrimarily in power generation, oil & gas, and manufacturing sectors
Job FocusMonitoring and adjusting control systemsOverseeing entire control room operations and coordination

Both Control Operators and Control Room Operators work in industrial environments monitoring control systems. Control Operators focus on operating specific control systems, while Control Room Operators oversee the entire control room operations, often managing multiple systems and coordinating team efforts.

Control Operator jobs near you
Infographic showing various Control Operator job openings in Linden, NJ as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 24% Part Time, 2% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $52,947 per year, or $25.5 per hour.

Quality Control Analyst

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 4 days ago

Job description

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs).  This role supports the day-to-day operations within the Quality Control group via execution of analytical testing. This includes but is not limited to in-process testing, lot release testing, stability testing, and raw material testing. All activities are all performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures.
 
This role will be a hands-on resource reporting to the Senior Director, Quality Control Bioanalytics.  
 
Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Conduct routine and non-routine analytical, biochemical, and/or biological analysis such as, in-process materials, raw materials, finished goods, or stability samples
  • Work with cell therapy products and associated assays (dPCR, qPCR, cell-based potency assays, proliferation assays, ELISA, flow cytometry assays, etc.)
  • Perform timely and accurate peer review of analytical test results/reports
  • Prepare COA/COT for testing performed
  • Identify discrepancies, initiate and investigate OOS/OOT results for phase 1 and phase 2
  • Initiate and investigate deviations related to quality control
  • Compile and review data to ensure accuracy and regulatory compliance
  • Support development for specifications and justification of specifications
  • Participate in validation and technical transfer of analytical methods commensurate with experience
  • Write and revise test methods
  • Maintain required training and training records and provide training to qualify other associates
  • Participate in internal assessments and audits as required
  • Support equipment validation, calibration, maintenance, and troubleshooting
  • Write method validation protocol/reports and other documentation such as test reports
  • Write stability protocol and stability reports
  • Write and revise Quality Control Standard Operating Procedures
  • Supply Quality Control data necessary for regulatory submissions
  • Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.
  • Assist in general upkeep of the laboratory and maintain a clean work environment
  • Perform other duties as assigned
Requirements
  • Bachelor's degree in a science discipline required, or comparable experience
  • 2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment, is preferred
  • Prior experience related to method development/validation
  • Prior experience with immune cell phenotyping by multicolor flow cytometry, dPCR, qPCR, cell-based potency and other cell therapy related assays is preferred
  • Knowledge of pharmaceutical cGMP (US and EU) is preferred
  • Must have excellent verbal, written, interpersonal, and organizational and communication skills
  • Must be able to commute to Bridgewater, New Jersey
  • Self-awareness, integrity, authenticity, and a growth mindset
$90,000 - $210,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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