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Qc Data Analyst Jobs (NOW HIRING)

Work closely with analysts and scientific staff to investigate and resolve data discrepancies, sample management questions, and documentation issues. * Maintain accurate QC review records in ...

Review and approval of cGMP analytical data comparing results to internal and customer specifications, SOPs, and established standards to ensure accuracy and quality of data * Collaborate with QC ...

ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our ... With moderate guidance, the Data Review Chemist II is responsible for utilizing the Quality ...

Quality Control Analyst

Norton, MA · On-site

$40 - $45/hr

Quality Control Analyst II Location: Norton, MA 02766 Duration: 12-Months Contract Pay: $40-$45/hr ... The role supports product quality, compliance, investigations, data trending, and laboratory ...

The Data Reviewer II is responsible for review and approval of primary analytical data according to ... Responsibilities * Review quality control testing for compliance with internal SOPs and ...

... analytical procedures and methods, and regular monitoring, trending, and reporting of QC data to support product quality and continuous improvement. Activities • Perform daily control sampling to ...

The Data Reviewer will be expected to review analytical data including XRPD, PSD, DSC, TGA, UV ... The position will also support QA initiatives when necessary and collaborate with laboratory ...

We are actively hiring a remote QC & Data Management Specialist. Shift: Monday-Friday Location: Remote Compensation: $24.00-$27.00 per hour FLSA Classification: Non-Exempt ESSENTIAL JOB FUNCTIONS:

Quality Control Analyst II

Rensselaer, NY

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to ...

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product ... Support investigations and deviations * Assist with stability studies and data analysis ...

Showing results 21-40

Qc Data Analyst information

See salary details

$34K

$82.6K

$136K

How much do qc data analyst jobs pay per year?

As of Sep 13, 2026, the average yearly pay for qc data analyst in the United States is $82,640.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $97,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Qc Data Analyst jobs?

For Qc Data Analyst jobs, the most frequently searched job titles are:

Manager, Quality Control & Data Entry

Tempe, AZ • On-site

Celerion
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

Full-time

Posted 12 days ago


Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz


Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Responsible for managing the data workflow through Quality Control (QC) and Data Entry (DE) for studies, maintains timelines for client deliverables and ensures regulatory compliance. Requires interface with other departments and/or sites. Requires interface with Sponsors.
Essential Functions
  • Responsible for staff management in accordance with the organization's policies and applicable laws
  • Responsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees
  • Communicate and provide support/guidance to appropriate groups/staff as required to ensure established, revised and/or new processes are followed to ensure quality on-time/zero defect standards
  • Plan, organize and facilitate workloads and schedules of staff to ensure that timelines are met and are compliant with regulatory and internal procedure requirements.
  • Attend and participate in study specific meetings related to study set up, timeline production and management, and study status
  • May be required to carry out study tasks, including but not limited to, complete QC review of source data and raw data for studies, performing accurate data entry, attending internal study initiation meetings to determine QC criteria and timelines for studies
  • Write QC and DE SOPs and Procedure guides and participate in SOP and Procedure Guide Reviews
  • Create and track metrics associated with QC and DE responsibilities
  • Present the QC processes to sponsors and auditors
  • Lead Process Improvement initiatives to improve the quality of the source data
  • Participate in regulatory inspections, audits and meet with Sponsors as required
  • Monitor process efficiency and implement process improvement as needed, including data flow and identification of error trends and resolutions.
  • Lead and/or participate in problem solving for the data collection, quality control and data entry processes.

Knowledge/Skills/Education/Licenses
  • Bachelor's degree in a related field is required.
  • 1-2 years of supervisory or trainer/leader experience required.
  • Knowledge of Good Clinical Data Management Practices, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 preferred
  • Ability to adjust hours to meet workload priorities
  • Strong process improvement skills and change management experience
  • Critical thinking skills
  • Clinical data experience preferred
  • **Equivalent education and experience will be consider

Celerion Values: Integrity Trust Teamwork Respect
Are you ready to join our team?
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
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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