About this opportunity
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
ob Description
Ensure that our product is functional and safe for the end customer by understanding, developing and
applying quality control systems, as well as analyzing, proposing and implementing improvement of
quality and manufacturing processes, thinking about improving defects in a timely and efficient manner
Evaluate, propose and implement high complexity improvements in processes in the process
quality area, seeking to strengthen processes while improving their efficiency, guided and advised
by the area manager .
Search for solutions to problems identified in the areas of manufacturing and process quality
through the application of Lean tools.
Support assigned root cause investigations (NCRs), as well as the development of action plans and
the implementation of corresponding actions, during the established period of time. Review and
Approve documents for High Impact NCR.
Develop and establish new processes and procedures from a quality perspective based on the Risk system evaluation, be part of the process and product transfer projects from the planning stage to its operationalization with high understanding of the ISO standard and other regulations.
Coach and train colleagues to achieve a high performance team following the department's
purpose, as well as make high-impact decisions evaluating the risk in the absence of the manager
Review and approve quality plans and First Article Plans related to the production process with low to high complexity, as well as propose changes to PFMEAs, this for those projects where you are assigned as a Quality representative.
Perform reviews to OT Core System documents as well as validation/qualification protocols (IQ,
PPQ, IOQ, IO, PR, etc.) where assigned as a quality representative complex and advance system.
Provide support to key company projects, including definition and implementation of controls
aimed at ensuring product quality.
Ensure the order and cleanliness of the areas under your responsibility. (5's) and comply with
quality GO's in the corresponding period.
Do the other functions inherent to the position and those assigned by your immediate manager.
Meet compliance with corporate and legal EHS requirements, by complying with internal policy and procedures. In addition, ensure compliance through the adoption of necessary strategies, internal controls, communication and training.
Continuously maintain EHS results through leadership, commitment and participation in all EHS-related initiatives.
Requisitos
Education:
Bachelors degree in Industrial Engineering Bussiness Administrator or related career.
Desirable CQE (CERTIFIED QUALITY ENGINEER certification) given by ASQ.
Intermediate/advanced English proficiency.
Experience:
Experience of at least 3-5 years as a quality
supervisor/quality engineer in the medical
industry.
Plus: Experience in product transfer, quality
system, validations and manufacturing, new
procedure definition, risk assessment
documentation development.
Skills:
Critical thinking
Focus on excellence
Open and authentic
Project management
Communication
Decision based on data analysis and Risk
approach
Advance Statistical Knowledge
Información adicional
AbbVie es un empleador que ofrece igualdad de oportunidades y se compromete a operar con integridad, impulsar la innovación, transformar vidas y servir a nuestra comunidad. Empleador que ofrece igualdad de oportunidades, veteranos y discapacitados.
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 1458 comparable Quality roles across 143 biopharma companies.
Salary context
256 of 1458 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1458 comparable roles
+ 47 more countries
Seniority mix
712 of 1458 peers have a known seniority level
Therapeutic area mix
2 of 1458 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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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.