About this opportunity
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.
Labcorp is seeking a QA Manager to join our team in Singapore BioA.
Job Responsibilities:
Plans and executes the necessary QA inspection programs to maintain local GLP/GCP compliance
Develops procedures as necessary to cover site GLP/GCP needs
Ensures recruitment and training of a competent and sufficient GLP/GCP QA workforce to meet business site needs
Accountable for budgetary oversight of the GLP/GCP QA team
Leads site communications with external Regulatory and Client compliance counterparts
Ensure the consistent implementation, use and review of SOPs
Escalate issues to management in a timely manner, implementing appropriate solutions including preventative actions
Negotiate with functional and operational internal stakeholders to improve quality and increase efficiencies
Analyse and interpret data to lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
Lead and effectively manage constructive crucial interactions with clients or regulatory agencies
Lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
Interpret applicable quality regulations/standards and create appropriate policies and procedures
Recruit, train, coach and develop individuals based on their development or business needs
Complete thorough, timely and well documented performance evaluations providing objective feedback to the individual
Ensure Regulatory Compliance and Quality Assurance (RC&QA) management responsibilities, as indicated in applicable controlled documents, are followed
Other duties as assigned by management
Minimum Qualifications:
Bachelor’s Degree in Life Science
8 years or more experience in GxP roles in a regulatory environment
Experience and regulatory expertise of industry quality systems/standards
Additional Job Standards:
Ability to interpret applicable regulations/standards
Experience in leading process improve initiatives
Ability to effectively communicate and influence internal stakeholders
Ability to supervise resources in a single geographic location
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 332 comparable Manager Quality roles across 82 biopharma companies.
Salary context
56 of 332 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 332 comparable roles
+ 34 more countries
Seniority mix
332 of 332 peers have a known seniority level
Therapeutic area mix
1 of 332 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.