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Manager, Quality Assurance

AbbVie Inc. - Heredia, Heredia Province, Costa Rica

Posted Jun 10, 2026

Benefits

Parental leave
12 weeks From the posting source
Non-birth-parent leave
12 weeks From the posting source
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
Not verified
Verification
Source-linked checked May 7, 2026
Salary
Not verified
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

Matched to SOC 11-1021 - Operations aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Operations From the posting source
Seniority
Senior From the posting source

Schedule

Shift type
Not verified
Weekend work
Not verified

Company

Equity
Offered Verified - SEC 10-K source

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Manager, Quality Assurance Heredia, Heredia Province, Costa Rica Descripción de la empresa: About AbbVie La misión de AbbVie es descubrir y ofrecer medicamentos y soluciones innovadores que resuelvan los problemas de salud graves de hoy y aborden los desafíos médicos del mañana. Nos esforzamos por tener un impacto notable en la vida de las personas en varias áreas terapéuticas clave, como la inmunología, la oncología y la neurociencia, y en los productos y servicios de nuestra cartera de productos de Allergan Aesthetics. Para obtener más información sobre AbbVie, visítenos en www.abbvie.com. Siga a @abbvie en LinkedIn, Facebook, Instagram, X y YouTube. Descripción del empleo: Provide technical direction and support on microbiology applied to the industry. Ensure an appropriate microbiological assessment is performed regarding changes that impact the manufacturing process or product. Manage the resources and capabilities of each area, as well as coordinate the execution of improvement, cost reduction, and risk reduction projects. Provide direction and support in root cause investigations and implementation of corrective and preventive action plans. Lead the proper execution and planning of the Internal Audit System in order to comply with requirements established in applicable regulations. Provide direction in the preparation and execution of external audits or inspections of the plant Quality System. Lead the proper administration of the facility's Corrective and Preventive Action system. Lead the proper functioning of the DHR area (complaint investigations) and the DAL laboratory (returned product analysis), as well as their compliance with applicable standards. Lead the proper functioning of the

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