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Change Control Manager Jobs in Temecula, CA (NOW HIRING)

DHL

Inventory Control Supervisor

Vista, CA · On-site

$55K - $90K/yr

  • Medical

  • Dental

  • Vision

  • PTO

If you're looking for change, and you're ready to make changes ... we're looking for you. DHL ... The Inventory Control Supervisor will assist site Inventory Control and Operations Leadership and ...

DPDHL

Inventory Control Supervisor

Vista, CA · On-site

$55K - $90K/yr

  • Medical

  • Dental

  • Vision

  • PTO

If you're looking for change, and you're ready to make changes ... we're looking for you. DHL ... The Inventory Control Supervisor will assist site Inventory Control and Operations Leadership and ...

Viasat, Inc.

Sr. Program Control Analyst

Carlsbad, CA · Hybrid

$148K - $222K/yr

At Viasat, we're on a mission to deliver connections with the capacity to change the world. For ... This role will report to the Program Control Manager. This is an exciting opportunity to support a ...

New

BOOZ, ALLEN & HAMILTON, INC.

Configuration Manager

Encinitas, CA · On-site

$61K - $141K/yr

  • Medical

  • Life

  • Retirement

  • PTO

You will maintain responsibility for ensuring that changes to the program's Configuration items (CI) are managed in accordance with the approved change control processes. You will maintain program ...

United Flow Technologies

Project Manager III

Temecula, CA · On-site

$125K - $180K/yr

  • Medical

  • Retirement

  • PTO

Change Control: Implement change control measures to manage modifications in project scope effectively * Schedule and Budget Management: Monitor and control project progress to ensure on-time and ...

United Flow Technologies

Project Manager III

Temecula, CA

$125K - $180K/yr

  • Medical

  • Retirement

  • PTO

Change Control: Implement change control measures to manage modifications in project scope effectively * Schedule and Budget Management: Monitor and control project progress to ensure on-time and ...

Bachem

Sr. Manager, Automation Engineer

Vista, CA · On-site

$107K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure compliant design, implementation, qualification, change control, documentation, and ... Manage automation department planning, resource allocation, vendor coordination, project priorities ...

Bachem

Sr. Manager, Automation Engineer

Vista, CA · On-site

$107K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Ensure compliant design, implementation, qualification, change control, documentation, and ... Manage automation department planning, resource allocation, vendor coordination, project priorities ...

JLL

Senior Facilities Manager

Oceanside, CA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience with validation protocols, qualification processes (IQ/OQ/PQ), and change control management in regulated environments * Familiarity with pharmaceutical manufacturing processes and how ...

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All JobsChange Control JobsChange Control Manager JobsChange Control Manager Jobs in Temecula, CA

Change Control Manager information

See Temecula, CA salary details

$38.7K

$81.6K

$123.7K

How much do change control manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for change control manager in Temecula, CA is $81,601.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,700.00 and $120,200.00 per year, depending on experience, location, and employer.

What are the typical challenges faced by a change control manager when coordinating cross-functional teams during change implementation?

A Change Control Manager often encounters challenges such as aligning diverse team priorities, ensuring clear communication, and managing resistance to change across departments. Coordinating cross-functional teams requires balancing the needs and schedules of stakeholders in IT, quality assurance, operations, and regulatory affairs. Successfully navigating these challenges involves setting transparent processes, hosting regular update meetings, and fostering a culture of collaboration to ensure changes are implemented smoothly and in compliance with relevant standards.

What are the key skills and qualifications needed to thrive as a change control manager, and why are they important?

To thrive as a Change Control Manager, you need expertise in project management, process improvement, and risk assessment, often supported by a relevant degree and certifications such as PMP or ITIL. Familiarity with change management software, documentation systems, and compliance tools is typically required. Strong communication, analytical thinking, and stakeholder management skills help drive successful change initiatives and mitigate resistance. These skills and qualities are crucial to ensure that organizational changes are implemented efficiently, with minimal disruption and maximum compliance.

What is the difference between Change Control Manager vs Quality Assurance Specialist?

AspectChange Control ManagerQuality Assurance Specialist
CertificationsISO 9001, PMP, or equivalentISO 9001, Six Sigma, or equivalent
Work EnvironmentRegulated industries like manufacturing, pharma, biotechManufacturing, software, healthcare sectors
Primary FocusManaging change processes, documentation, approvalsEnsuring product quality, testing, compliance

The Change Control Manager and Quality Assurance Specialist roles often overlap in regulated industries, but their focus differs. The Change Control Manager primarily oversees change processes and documentation, ensuring compliance with procedures. The Quality Assurance Specialist concentrates on maintaining product quality through testing and compliance checks. Both roles require similar certifications and work environments, but their core responsibilities distinguish them within the industry.

What is a change control manager?

Change Control Managers are professionals responsible for overseeing and managing the process of controlling changes to projects, systems, or processes within an organization. Their main role is to ensure that all proposed changes are properly evaluated, documented, and implemented in a controlled manner to minimize risks or disruptions. They work closely with project teams, stakeholders, and quality assurance to ensure compliance with regulatory requirements and organizational standards. This role is especially vital in industries like IT, pharmaceuticals, and manufacturing, where changes can significantly impact operations or product quality.

What are popular job titles related to Change Control Manager jobs in Temecula, CA?

For Change Control Manager jobs in Temecula, CA, the most frequently searched job titles are:

What job categories do people searching Change Control Manager jobs in Temecula, CA look for?

The top searched job categories for Change Control Manager jobs in Temecula, CA are:

What cities near Temecula, CA are hiring for Change Control Manager jobs?

Cities near Temecula, CA with the most Change Control Manager job openings:

Change Control Manager jobs near you
Infographic showing various Change Control Manager job openings in Temecula, CA as of June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $81,601 per year, or $39.2 per hour.

Manager, Quality - QC Analytical

Glaukos

San Clemente, CA • On-site

Full-time

Re-posted 14 days ago

Job description


How You'll Make an Impact:
The Quality Control Manager in San Clemente, CA oversees all QC laboratory operations and testing activities. This role supervises QC staff, ensures compliant and efficient lab execution, maintains cGMP compliance and data integrity, and provides technical leadership while keeping the laboratory inspection-ready and supporting project teams as needed.
What You'll Do:
General laboratory Management
  • Oversees and assigns raw material, in-process, finished product, and stability testing across multiple pharmaceutical products to ensure timely batch release and stability commitments
  • Manages cGMP stability programs for clinical and commercial products and performs trend analysis to identify risks or emerging issues
  • Oversees the internal reference standard qualification, lifecycle management, and documentation program
  • Oversees method validations, verifications, transfers, and feasibility studies to support product development and commercialization
  • Oversees audit trail review process and 21 CFR Part 11 compliance
  • Evaluates internal versus external testing strategies and recommends improvements to optimize efficiency, cost, and compliance
  • Recommends laboratory equipment, instrumentation upgrades, and new technologies to support future QC capability needs
  • Oversees qualification and calibration of analytical equipment and approves vendor qualification documentation, may include URS development, IQ/OQ/PQ approval authority, equipment lifecycle planning, obsolescence strategy
  • Monitors contract testing laboratories, reviews external analytical data, and ensures CRO/CMO compliance with quality standards
  • Identifies and resolves technical challenges impacting method transfer, assay implementation, and laboratory operations
  • Responsbile for laboratory budget management such as headcount forecasting, consumables planning, and alignment on capital expenditure planning

Documentation & Compliance
  • Reviews and approves analytical data, laboratory documentation, and Certificates of Analysis to ensure accuracy, completeness, and data integrity
  • Oversight of audit trail review process
  • Authors and/or reviews laboratory investigations (OOS, OOT, deviations) and ensures appropriate root cause analysis, impact assessment, and corrective actions
  • Authors, reviews, and approves analytical methods, validation protocols, qualification reports, and stability reports to ensure regulatory compliance
  • Provides annual product quality review analytical input
  • Ensures QC documentation, laboratory systems, and practices comply with ICH, USP, Pharm. Eur., JP, and applicable global regulatory guidelines
  • Supports regulatory submissions by preparing or reviewing technical summaries
  • Contributes to SOP development, process improvements, and continuous improvement initiatives within the laboratory

Inspection Readiness & Regulatory Activities
  • Ensures QC maintains inspection readiness, compliance, and a culture of data integrity
  • Serves as the primary technical lead for QC investigations and escalates significant quality risks appropriately
  • Analyzes and interprets complex analytical data and provides scientifically sound conclusions to support quality and regulatory decisions
  • Participates in regulatory inspections and supports responses to regulatory agencies as required
  • Owns QC laboratory performance metrics and drives continuous improvement initiatives to improve efficiency and compliance

Team Leadership & Cross-Functional Support
  • Supervises QC chemists, sets priorities, and ensures compliant execution of laboratory activities in accordance with cGMP requirements
  • Responsible for QC chemist training matrix updates in coordination with training team
  • Provides technical leadership, mentorship, development, and performance management for QC chemists
  • Participates in cross-functional development and manufacturing meetings as QC representative
  • Communicates QC priorities, timelines, and risks to stakeholders and leadership
  • Collaborates with R&D to assess and implement specialized analytical approaches, when applicable
  • Ownership of QC lab related change control or technical impact assessments and CAPA approval authority
  • Employing technical knowledge to assist with Quality risk management (FMEA) and risk management during Quality investigations

Digital and Automation Strategy
  • Oversee implementation of LIMS / electronic notebooks
  • Improve digital data analytics

How You'll GetThere:
  • 8+ years of experience in analytical chemistry within Pharmaceutical QC environment.
  • Minimum of 1 year of previous management experience in Pharmaceutical QC laboratory, including supervision of QC chemists.
  • Demonstrated leadership skills with the ability to prioritize workload, mentor staff, and ensure inspection readiness and cGMP compliance.
  • Experience managing and overseeing external contract testing laboratories (CROs/CMOs) is preferred.
  • Understanding of analytical platforms including HPLC, FTIR, UV/Vis, and Drug Release.
  • Experience overseeing analytical method validation, verification, method transfer activities, and management of cGMP stability programs.
  • Working knowledge of ICH guidelines, major pharmacopoeias (USP, Ph. Eur., JP), CTD structure, and global regulatory expectations.
  • Strong analytical skills (interpret data, summarize data, present data).
  • Strong written and verbal communication skills. •
  • Motivated and able to work independently, as well as within a team. Exhibits personal integrity, credibility, and responsibility. •
  • Excellent organizational skills and ability to work on multiple projects/tasks. •
  • Meets milestones and schedules.
  • Bachelor's degree in a scientific discipline is required

#GKOSUS
About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.
Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.
Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.

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