LabCorp

QualityReviewerII

Bangalore, Karnataka, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Quality Reviewer II at LabCorp. Skills: Quality Review, Process Improvement, Customer Complaints. Follow applicable departmental SOPs. Perform quality check of tasks”

What You'll Achieve.

Ensure consistency in compliance; resolution of all customer complaints; prevent errors; reduce costs

Industry & Context.

Problems you'll solve

Manage and solve changes; Manage and solve issues; Manage and solve concerns; problem-solving skills

What They're Looking For.

Must Have

Bachelor’s degree in life science

Nice to Have

3 years’ experience in a quality review environment, medical technology experience, medical science experience, 3 years’ experience with the clinical trial process, relevant experience in the pharmaceutical industry

What You'll Do.

Follow applicable departmental SOPs

Perform quality check of tasks

Provide timely feedback to associate

Assist QC lead in preparing QC trend analysis

Assist QC lead in updating escalation tracker

Identify process steps/gaps

Suggest steps to improve quality compliance

Support team in preparing CAPA

Ensure consistency in compliance

Monitor and ensure resolution of customer complaints

Support a culture of continuous improvement

Participate in process improvement initiatives

Liaise with team members

Pursue understanding of services

Manage and solve changes

Manage and solve issues

Manage and solve concerns

Participate in team tasks

Execute operational activities

Give technical advice

Work collaboratively on a team

How You'll Work.

Team & Collaboration

cross-functional coordination; vendor/stakeholder management; work collaboratively on a team; liaising with team members

Communication Scope

Provide timely feedback

Full Job Description

LabCorp is seeking a Quality Reviewer II to join our team at the Bangalore Site in Bangalore, Karnataka. **Work Schedule** 40hrs a week (Monday to Friday) in a rotational shift. **Job Responsibilities** Follow applicable departmental Standard Operating Procedures and Work Instructions. Perform quality check (QC) of tasks for the identified team and provide timely feedback to the concerned associate, with copy to their manager. Assist QC lead in preparing QC trend analysis report. Assist QC lead in updating and maintaining the the escalation tracker. Identify process steps/ gaps that lead to quality errors and suggest steps to improve quality compliance. Support the team in preparing a CAPA for QC observations. Ensure consistency in compliance to our standard procedures to members of the team *Monitor and ensure resolution of all customer complaints, issues, and concerns. Support a culture of continuous improvement and quality. Act as a contributing core team member by participating in process improvement initiatives and liaising with team members *Responsible for pursuing an understanding of services related to the different clusters and client-specific requests. Manage and solve changes, issues, and concerns of varied complexity, work with little to no guidance, but require some guidance for complex work. Participate in team tasks related to executing operational activities Demonstrate ability to mentor, give technical advice, work collaboratively on a team, and assist with training. **Minimum Qualifications** Bachelor’s degree in life science **Preferred Qualifications** 3 years’ experience in a quality review environment, medical technology, or medical science experience, or 3 years’ experience with the clinical trial process or relevant experience in the pharmaceutical industry **Additional Job Standards** Focus on customer (1): Understands and Considers: Consistently and continuously respond and show understanding of the clients' "world" and their immediate nee

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