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Process Control Manager Jobs in Phoenix, AZ (NOW HIRING)

EMCOR Group, Inc.

QA/QC Manager

Tempe, AZ · On-site

Our expertise includes design-assist, HVAC, plumbing, sheet metal, and process piping construction ... The QA/QC Manager is responsible for ensuring compliance with industry codes, project ...

QTS Realty Trust, Inc.

Cost Control Manager

Phoenix, AZ · On-site

The Cost Control Manager is responsible for managing construction budgets from project inception ... Support the finance team with the monthly loan draw process as required, including acquiring any ...

Pkaza

Data Center Construction QA / QC Manager

Mesa, AZ

$82K - $110K/yr

Data Center Construction QA / QC Manager - Mesa, AZ This opportunity is with a leading EPC Company ... Must have experience analyzing processes, creating process documentation, developing operational ...

New

Actalent

Qa/qc Manager

Phoenix, AZ

Job Title: QA/QC Manager The QA/QC Manager leads quality assurance and quality control efforts ... Coordinate and oversee inspections, testing activities, and quality verification processes to ...

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All JobsProcess Control JobsProcess Control Manager JobsProcess Control Manager Jobs in Phoenix, AZ

Process Control Manager information

See Phoenix, AZ salary details

$37.2K

$100.2K

$138K

How much do process control manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for process control manager in Phoenix, AZ is $100,212.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,400.00 and $112,200.00 per year, depending on experience, location, and employer.

What is a process control manager?

A Process Control Manager is responsible for overseeing and optimizing the various control systems and processes used in manufacturing or industrial operations. Their role involves ensuring that production processes run smoothly, efficiently, and safely by managing automated systems, monitoring performance, and implementing improvements. They often work closely with engineering, production, and quality assurance teams to identify issues and enhance process reliability. Additionally, they may be involved in training staff, maintaining compliance with regulations, and deploying new technologies to improve process control.

What are the key skills and qualifications needed to thrive as a process control manager?

To thrive as a Process Control Manager, you need a strong background in engineering or process technology, analytical problem-solving abilities, and experience in manufacturing or industrial environments. Familiarity with distributed control systems (DCS), programmable logic controllers (PLCs), process automation software, and often certifications like Six Sigma or PMP are highly valued. Excellent leadership, communication, and decision-making skills help manage teams and coordinate with cross-functional departments effectively. These competencies are vital for ensuring process efficiency, safety, quality, and continuous improvement within complex production operations.

What are some typical challenges a process control manager might face in a manufacturing environment?

Process Control Managers often encounter challenges such as integrating new technologies with legacy systems, maintaining process consistency across shifts, and troubleshooting unexpected process deviations. They must also ensure compliance with safety and quality standards while coordinating closely with engineering, production, and maintenance teams. Strong problem-solving skills and effective communication are essential for navigating these complexities and driving continuous improvement initiatives.

What is the difference between Process Control Manager vs Process Engineer?

AspectProcess Control ManagerProcess Engineer
CredentialsBachelor's degree in engineering, certifications in process control (e.g., Certified Control Systems Technician)Bachelor's or master's in chemical, mechanical, or industrial engineering; certifications vary
Work EnvironmentSupervises control systems teams, manages process control strategies in manufacturing plantsDesigns, develops, and optimizes manufacturing processes, often in labs or plant settings
Employer & IndustryManufacturing, oil & gas, chemical industriesChemical, pharmaceutical, manufacturing industries

The Process Control Manager oversees the implementation and maintenance of control systems, focusing on team management and strategy. In contrast, the Process Engineer concentrates on designing and improving processes. Both roles require technical expertise but differ in scope and responsibilities.

What are popular job titles related to Process Control Manager jobs in Phoenix, AZ?

For Process Control Manager jobs in Phoenix, AZ, the most frequently searched job titles are:

What job categories do people searching Process Control Manager jobs in Phoenix, AZ look for?

The top searched job categories for Process Control Manager jobs in Phoenix, AZ are:

What cities near Phoenix, AZ are hiring for Process Control Manager jobs?

Cities near Phoenix, AZ with the most Process Control Manager job openings:

Process Control Manager jobs near you
Infographic showing various Process Control Manager job openings in Phoenix, AZ as of August 2026, with employment types broken down into 74% Full Time, and 26% Part Time. Highlights an 100% In-person job distribution, with an average salary of $100,212 per year, or $48.2 per hour.

Quality Control Manager, Sterile

Mesa, AZ • On-site

Hims and Hers Health, Inc.
See more jobs at Hims and Hers Health, Inc.external

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 16 hours ago

Key responsibilities

  • Oversee sampling, testing, and documentation of sterile drug products to ensure they meet quality, safety, and regulatory standards.

  • Manage quality control shop floor activities, including environmental and process monitoring, to ensure compliance with relevant standards and procedures.

  • Collaborate on investigations of out-of-specification results, sterility failures, and environmental excursions, and document corrective actions.

Job description

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve.
Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.
About the Role: The Quality Control (QC) Manager is responsible for overseeing and executing all QC shop floor activities to ensure compounded sterile preparations (CSPs) meet established quality, safety, and regulatory standards. This role ensures compliance with USP <795>, USP <797>, USP <800>, state board requirements, and FDA guidance applicable to 503A sterile compounding environments. The QC Manager works closely with the Pharmacist in Charge, Quality Assurance, Microbiology, Compounding Operations, and Pharmacy leadership to maintain a robust quality control program that protects patient safety and supports continuous improvement.
Schedule: Monday - Thursday 7am - 5:30pm
You Will:
Product Testing & Release
  • Oversee sampling, testing, and documentation of sterile drug products for sterility, endotoxin, potency, identity, particulate matter, and pH, as applicable.
  • Manage coordination with third-party analytical laboratories, including sample submission, data review, and investigation of test abnormalities.
  • Review and approve Certificates of Analysis (COAs) and ensure results meet specifications prior to product release.
Environmental & Process Monitoring
  • Manage quality control shop floor activities during compounding operations to ensure appropriate coverage over all shifts.
  • Ensure the quality control team remains compliant with gowning, line clearance, and visual inspection competency assessments and qualifications, along with other required training.
  • Provide guidance to quality control team on room clearance, line clearance and Acceptable Quality Level (AQL) inspections
  • In collaboration with Microbiology, supervise viable and non-viable environmental monitoring in ISO-classified areas in accordance with USP <797>.
  • Oversee personnel monitoring (gloves, gowns, fingertip sampling) and ensure compliance with established frequency and limits.
  • Trend environmental monitoring data and implement corrective actions for excursions.
Deviation, OOS, and Investigation Management
  • Collaborate with Microbiology and Pharmacist in Charge on investigations for out-of-specification (OOS) results, sterility failures, and environmental excursions
  • Conduct and document event investigations and root-cause analyses; propose and verify effectiveness of corrective and preventive actions (CAPA).
  • Ensure investigations are timely, compliant, and thorough prior to seeking pharmacist approval
Documentation & Record Control
  • Ensure quality batch record review checklists are completed in accordance with internal processes and procedures.
  • Maintain accurate quality records, logs, test results, and retain sample documentation.
  • Ensure data integrity principles (ALCOA+) are followed across all QC-related records.
  • Support revision and creation of SOPs and work instructions related to QC operations.
Equipment Oversight
  • Collaborate with the microbiology manager on qualification, calibration, and maintenance of QC instruments (e.g., particle counters, incubators, pH meters, balances).
  • Ensure appropriate compounding equipment logs, preventive maintenance, cleaning and calibration files are maintained and up-to-date.
Quality Systems Support
  • Partner with the Pharmacist in Charge and QA to support audits, mock inspections, and regulatory inspections.
  • Participate in risk assessments, change controls, and continuous improvement meetings.
  • Support training of pharmacy staff on quality compliance requirements and aseptic principles.
Operational Support
  • Provide technical and shop floor support to sterile compounding personnel related to testing requirements, sampling, and product specifications.
  • Ensure proper handling, storage, and disposal of testing materials, media, and reagents.
  • Monitor trends to identify opportunities to enhance sterility assurance and product quality.

You Have:
  • Bachelor's degree in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, or related field.
  • Minimum 3-5 years of QC experience in a sterile compounding, pharmaceutical, or biotech environment.
  • Strong knowledge of USP <795>, USP <797>, USP <800>, cGMP, and state pharmacy regulations.
  • Experience with laboratory investigations, root-cause analysis, and CAPA processes.
  • Demonstrated ability to interpret analytical data and laboratory test results.
  • Excellent documentation skills and attention to detail.

Preferred Qualifications
  • Experience working directly in a 503A compounding pharmacy or 503B outsourcing facility.
  • Familiarity with FDA guidance on sterile compounding.
  • Supervisory experience or the ability to lead and develop QC staff.
  • Experience with LIMS or electronic quality systems.
Core Competencies
  • Quality-focused decision-making
  • Strong problem-solving and analytical ability
  • Aseptic knowledge and high attention to detail
  • Effective communication and collaboration across pharmacy and quality teams
  • Ability to manage multiple priorities in a fast-paced, regulated environment
Our Benefits (there are more but here are some highlights):
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO and company holidays
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching contribution

Conditions of Employment:
  • This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required.
  • This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).
  • Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve-hour shift. Must be able to lift up to 50lbs.
  • Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

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