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Change Control Analyst Jobs (NOW HIRING)

QC Analyst III

Piscataway, NJ · On-site

$24 - $32.25/hr

Preparation and routing the change control documents as required. Requirements Position ... analytical results. • Demonstrated success at writing, revising, and complying with SOPs ...

QC Analyst III

Piscataway, NJ

$24 - $32.25/hr

Description Position Summary The QC Analyst III will be responsible for analytical testing and data ... Preparation and routing the change control documents as required. Requirements Position ...

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 · 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 ...

Support the change management process for respective front office coverage areas. * Maintenance and ... control analysis, metric reporting, scenario analysis, stress testing, etc.) * Assist Senior ...

Quality Control Analyst

Bridgewater, NJ

$24.50 - $33/hr

Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

The Quality Control Analyst I will perform routine quality testing activities in a QC laboratory ... Support deviations, CAPAs, and change control processes. * Report issues and assist in incident ...

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 ...

Able to lead, influence and negotiate with a team and/or senior management to drive change. Impact ... Analysis, Control Testing Framework, End-to-End Process & Controls reviews, and New Business ...

The Material Control Analyst will be responsible for material ordering, tracking and expediting to ... While subject to change based on business needs, Leidos reasonably anticipates that this job ...

The Material Control Analyst will be responsible for material ordering, tracking and expediting to ... While subject to change based on business needs, Leidos reasonably anticipates that this job ...

The Material Control Analyst will be responsible for material ordering, tracking and expediting to ... While subject to change based on business needs, Leidos reasonably anticipates that this job ...

An IT Analyst on the Production Control team is responsible for working within the team, other IT ... Change, Release and Deployment Management * Manage the IT service management lifecycle to enable ...

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Change Control Analyst information

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How much do change control analyst jobs pay per hour?

As of Jun 12, 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.

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.

What are Change Control Analysts?

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, and why are they important?

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.
What states have the most Change Control Analyst jobs? States with the most job openings for Change Control Analyst jobs include:
What job categories do people searching Change Control Analyst jobs look for? The top searched job categories for Change Control Analyst jobs are:

$24 - $32.25/hr

Full-time

Posted 27 days ago


Job description

Job Type
Full-time
Description
Position Summary
The QC Analyst III will be responsible for analytical testing and data verification/review supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required.
Essential Duties & Responsibilities
  • Analytical testing to support product in-process, release, and stability programs.
  • Perform the data verification/Review process as assigned.
  • Participate in Method Validation activity.
  • Preparation of the Protocols/Reports as assigned.
  • Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.
  • Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.
  • Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards
  • Preparation and routing the change control documents as required.

Requirements
Position Requirements and Qualifications
Education:
• Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 10 years of experience in a pharmaceutical/biotech QC laboratory. Alternatively, master's degree in above areas with 8 years of experience in a pharmaceutical/biotech QC laboratory.
Experience:
• Previous experience in a cGMP laboratory.
• Strong background in small molecule and protein chemistry and experience troubleshooting analytical results.
• Demonstrated success at writing, revising, and complying with SOPs, policies, and QC methods.
Specialized Knowledge and Skills:
• Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays.
• Knowledge of and experience with Empower and/or Shimadzu software
• Previous experience supporting regulatory inspections (e.g. PAI).
• Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies.
Work Environment & Physical Demands:
General Working Environment:
• Some time spent in an office doing office work (reading, writing, reviewing, and editing documents).
• Significant amount of time spent in the laboratory.
• Must be able to work extended hours or weekend hours, as may be required.
Noise:
• No extraordinary noise levels.
Standing/Lifting:
• Must be able to lift at least 25 lbs.
Visual:
• No extraordinary requirements.
Stress:
• High-paced demanding environment to meet ambitious project goals.
Travel:
• No travel required.
Supervisory Responsibility, if any : No
This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.