Senior Manager, Third Party Manufacturing
About this opportunity
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube
Job Description
AbbVie is seeking a Senior Manager, External Manufacturing to lead the relationship with and
performance of its third-party manufacturers.
In this strategic and operational role, you will serve as AbbVie's primary point of contact for several
industrial partners. You will directly contribute to ensuring continuity of supply, quality, regulatory
compliance, manufacturing performance, and cost competitiveness for externally manufactured
products.
This opportunity is suited to someone who wants to grow within a multicultural organization that
combines agility, commitment, and speed of execution.
This role can be based in any of our 5 manufacturing sites across Ireland (Cork, Dublin, Sligo or Westport).
Key responsibilities
Manage relationships with third-party manufacturers by defining effective governance,
responsibilities, operating models, and communication channels.
Ensure continuity of supply by coordinating forecasts, production schedules, and delivery plans with Supply Chain, Planning, and industrial partners.
Anticipate and manage operational risks related to capacity, raw materials, components, lead times, or supplier performance to prevent supply disruptions.
Lead governance and operational performance through Virtual Operations Teams (VOTs), business
reviews, and steering committees with third-party manufacturers.
Define, monitor, and improve performance indicators covering quality, service, cost, capacity, and
lead times, and coordinate the associated action plans.
Drive issue resolution and required escalations, preparing reports and executive summaries for
management.
Ensure compliance with quality and regulatory requirements in close collaboration with Quality
teams and manufacturing partners.
Coordinate audits, inspections, annual quality reviews, deviations, investigations, and CAPAs,
ensuring corrective actions are implemented within expected timelines.
Contribute to product release and decision-making regarding potential non-conformities.
Lead technology transfers and strategic projects related to external manufacturing, process
changes, and manufacturing performance improvement.
Coordinate internal teams and industrial partners throughout projects, managing risks, timelines,
resources, costs, and communication.
Support products throughout their lifecycle and identify opportunities to improve reliability,
manufacturing robustness, and profitability.
Qualifications
Degree in Engineering or a scientific discipline
Minimum 7 years of experience in the pharmaceutical, biotechnology, or related regulated industry
Sterile manufacturing experience (mandatory)
Aseptic processing experience (mandatory)
Technology transfer experience (mandatory)
Strong project management and supplier management skills
Excellent stakeholder management, negotiation, and communication capabilities
GMP and quality systems knowledge
Internal grades may vary depending on country.
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 Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 452 comparable Manager Manufacturing & CMC roles across 73 biopharma companies.
Salary context
141 of 452 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 452 comparable roles
+ 25 more countries
Seniority mix
452 of 452 peers have a known seniority level
Therapeutic area mix
3 of 452 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.
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.