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Change Control Analyst Jobs (NOW HIRING)

QC Analyst III

Portsmouth, NH ยท On-site

$33/hr

Job Title: QC Analyst III Location: Portsmouth, NH - 100% On-Site Pay Rate: $33.00/hour We're ... Author Deviations, CAPA, Change Controls, and Test Methods. * Train peers on QC processes and ...

QC Analyst III

Portsmouth, NH ยท On-site

$25 - $30/hr

Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 months Job Type: Temporary ... Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods * Projects - such as ...

Quality Control Analyst

Monroe, NC ยท On-site

$22.25 - $30/hr

Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in ... versed with Change control/deviations and market compliant management system. Skills in ...

Our client is looking for an experienced Project Control Analyst to join their Program Finance ... change control. * Assist in the development of Work Breakdown Structures (WBS) and related ...

Quality Control Analyst III/IV

Seattle, WA ยท On-site

$27.25 - $36.75/hr

Perform general activities in accordance to SOPs and laboratory quality systems, including change ... Quality Control Analyst III: * BS/MS in a biological science or equivalent level of expereince.

Senior Change Analyst

Orangeburg, NY ยท On-site

$100K - $120K/yr

Determines how to improve and maintain the Change Control System and associated processes. Acts as the primary interface between engineering, manufacturing, field service, marketing, etc. to ensure ...

Strong knowledge of document control systems, engineering change management, configuration ... Strong analytical, organizational, problem-solving, and project management skills with exceptional ...

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Change Control Analyst information

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How much do change control analyst jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for change control analyst in the United States is $36.35, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $41.35 per hour, depending on experience, location, and employer.

What is a change control analyst?

Change Control Analysts are professionals responsible for managing and coordinating changes to processes, systems, or products within an organization. They ensure that all changes are properly reviewed, documented, and implemented according to established protocols to minimize risk and disruption. Their work often involves collaborating with various departments, tracking change requests, and maintaining compliance with industry standards. Change Control Analysts play a critical role in quality assurance, especially in regulated industries like pharmaceuticals, IT, and manufacturing.

What are the key skills and qualifications needed to thrive as a change control analyst?

To thrive as a Change Control Analyst, you need strong analytical skills, attention to detail, and a background in business, IT, or related fields, often supported by a relevant degree. Familiarity with change management software (like ServiceNow), ITIL certification, and document control systems is typically required. Excellent communication, organizational skills, and the ability to collaborate across departments set top performers apart. These skills ensure that changes are evaluated, documented, and implemented efficiently, minimizing risk and maintaining compliance within organizational processes.

How does a change control analyst collaborate with other departments during the change management process?

A Change Control Analyst regularly works with cross-functional teams, including IT, quality assurance, operations, and project management, to ensure that proposed changes are assessed comprehensively. They facilitate meetings to gather input, document risks, and ensure all stakeholders understand the impact of changes. Effective collaboration is essential for coordinating approvals, scheduling implementations, and minimizing disruptions to business operations.
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Infographic showing various Change Control Analyst job openings in the United States as of September 2026, with employment types broken down into 76% Full Time, and 24% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $75,608 per year, or $36.4 per hour.

QC Analyst III - Portsmouth, NH

Portsmouth, NH โ€ข On-site

Unicon Pharma Inc.
Recruiting and Staffing Servicesย โ€ขย 11 - 50 employees

$24.50 - $32.75/hr

Contractor

Re-posted 4 hours ago


Job description

Description:

Ideally on-site or hybrid - local candidate

  • The Quality Microbial Control Analyst V will act as a team member of the Quality Microbial Control department to support production of in-process and final product drug lots for customers. Also participate in quality testing for ongoing customer stability studies.
  • Provide on-time, high quality results to meet Manufacturing demands.
  • Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. May be assigned to work on special projects. Also may provide support to others in the absence of the supervisor.
  • Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required.
  • Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
    Acts as an area SME providing technical support within the department and throughout the facility.
  • Applies job skills and company's policies and procedures to complete a variety of tasks.
  • Running test samples for In-Process, Lot Release and Stability studies.
  • Support Utility and HVAC monitoring and sampling throughout the facility
  • Reviewing assays.
  • Training others.
  • Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods.
  • Projects – such as method transfers, new instruments, method qualifications.
  • Use of Microsoft Suites (Word, Excel, PowerPoint).
  • Use of Laboratory computer systems.
  • Potential previous use of GMP Quality Systems such as: TrackWise, LIMS.
  • Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required.
  • Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
  • Apply Data Integrity principles in all aspects of work, in compliance with Lonza DI policies, guidelines and procedures.
  • Perform other duties as assigned.
  • Back-up to Supervisor – Independently making quality decisions with input
  • Bachelor's Degree - Microbiology, Biochemistry or Related Science Fields
  • 5-10 years experience