Manager Post Market Quality Assurance F/M
About this opportunity
Company Description
AbbVie a pour mission de découvrir et d’offrir des solutions et des médicaments innovants pour répondre à des besoins importants en matière de santé aujourd’hui et relever les défis médicaux de demain. Elle met tout en œuvre afin d’avoir un impact remarquable sur la vie des gens dans divers aires thérapeutiques clés: l’immunologie, l’oncologie, les neurosciences, et les soins oculaires/les maladies de l'oeil, de même que dans le domaine de l’esthétique avec le portefeuille des produits et services d’Allergan Aesthetics. Pour en savoir plus sur AbbVie, visitez le site www.abbvie.com. Suivez @abbvie sur Twitter, Facebook, Instagram, YouTube et LinkedIn.
Job Description
Under the responsibility of the Quality Director, your role will be to act as one of the Site Quality representatives for commercialized AbbVie products and the global supply chain, with a dedicated team under your supervision.
In this role, you will have the following responsibilities:
• Act as the primary quality representative for the global supply chain and make decisions regarding product quality in alignment with various stakeholders (both local and global)
• Oversee and implement the global post-market surveillance strategy, including the development and analysis of PSURs (Periodic Safety Update Reports) and the management of PMCF (Post Market Clinical Follow-up), in order to anticipate risks, identify areas for improvement, and guide organizational decisions
• Oversee and implement the global complaint management strategy and review of market signals by strengthening a proactive approach to anticipate and evaluate customer satisfaction
• Oversee and implement the supplier quality strategy to select, evaluate, and develop high-performing partners to meet our objectives of excellence, innovation, and compliance with standards • Be responsible for the implementation and maintenance of the quality system’s effectiveness by applying and maintaining quality policies, procedures, and systems within your scope
• Guarantee the coordination of activities related to major quality events, ensuring alignment, engagement, and involvement of global stakeholders in key decisions • Manage stability programs, integrate and leverage collected data, and guide actions to ensure product reliability and durability • Lead the implementation of trend reviews, issue quality recommendations supporting the vision and mission of AbbVie Quality
• Conduct audits, monitor KPIs, and deploy action plans
• Establish and manage the budget for your department
• Manage a multidisciplinary quality team. Engage and mobilize your team with a collaborative team-working, performance, and ownership mindset.
Qualifications
You have the following strengths to join us:
Advanced scientific degree (Master’s degree or higher required) or pharmacist.
Minimum of 10+ years in quality assurance operations management, regulatory affairs, operations, or technical support in a pharmaceutical environment.
Knowledge of FDA, ISO13485 requirements for medical devices or pharmaceuticals.
Fluent in English (spoken and written).
Organizational/management skills and the ability to manage a team
Strong interpersonal skills for effective communication and teamwork
Ability to synthesize information and present it
Analytical and problem-solving skills, positive interpersonal skills, ability to manage multiple complex tasks simultaneously, and act as a leader and team member.
Solid knowledge in quality assurance/control, manufacturing, laboratory, technical support, regulatory affairs, and/or validation is required.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
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 164 comparable Manager Quality roles across 51 biopharma companies.
Salary context
44 of 164 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 164 comparable roles
+ 18 more countries
Seniority mix
164 of 164 peers have a known seniority level
Therapeutic area mix
0 of 164 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
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.
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.