AbbVie Posted November 5, 2026

Associate Director MSAT PDS&T

Waltham, MA Full-time
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AbbVie is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

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

​​The Associate Director, Technical position within the Product, Development, Sciences and Technology (PDS&T) organization is responsible for providing technical leadership, direction and management of the PDS&T teams.  The manager will provide technical expertise for commercial manufacturing during development of new products, manage operation and commercial timelines, and executes budgets for global projects and the team.  The Technical Manager establishes goals that are consistent with the department, development, manufacturing and customer requirements, implements plans and policies, assigns duties and responsibilities and controls subordinates performance to meet the goals and commitments.​

Responsibilities:

​​Provides technical leadership for multiple PDS&T projects and is responsible for financial planning, budget responsibility and timeline estimates of the project as well as execution.

Responsible for implementation of global projects across AbbVie plants and marketed affiliates this includes both AbbVie plants and products manufactured at Third Party Manufacturers (TPMs)

Provides technical expertise for marketed products and can represent the company in discussions with regulatory agencies.  Due to nature of the projects and support of marketed products, the impacts of decisions are significant to AbbVie's pharmaceutical Operations ($1B) to minimize back orders and regulatory risks.

Each technical function is responsible for providing support for marketed products including those related to transfer of new chemical entities from R&D to various manufacturing plants as well as process improvement and CMC support of marketed products. The role also includes transfer of marketed products between manufacturing plants and TPMs as required by the demands of Global manufacturing and product sourcing strategies.

Leads the team that handles complex technical projects.  These projects generally impact a significant portion of the business, are shared among multiple plants and/or markets.  The team provides a high level of technical expertise required for support of various regulatory organizations and market needs and has a global approach in implementation of projects to ensure consistency.  Teams within these functions have global responsibility (50+ markets), support multiple plants and/or markets.

The scope of activities for these teams includes interactions with R&D, Operations, Quality, Commercial and regulatory as well as the relevant technical plant support functions both within AbbVie and at third party manufacturers.

Works directly with multiple groups in a matrix approach to ensure that the overall objectives of the MS&T organization are met.  These include the provision of seamless and effective technology transfers across AbbVie manufacturing facilities globally, the development of cost effective, robust and compliant processes and ensuring that customer services and customer support remain uninterrupted.

Management of a technical team of multiple scientists and technicians ranging from scientist to senior level scientists.  The group is responsible for providing technical expertise for all regulatory and quality documentation as well as post approval filings.

The global nature of the job requires the position to have an excellent knowledge of various regulatory and GMP requirements as well as outstanding communication skills.  The position requires interaction with scientists from various sites and at times frequent traveling to support the projects.

​​

Qualifications

​​BSc degree in a scientific or technical field preferably in Life sciences, pharmacy or engineering required. Masters Degree and/or PhD is preferred.

Ten (10) + years in the Pharmaceutical Industry with at least 5 years working in relevant support group is required. Experience in support of marketed products is preferred.

The Technical Manager must display managerial ability via leadership, supervisory experience and administration.

Exhibits a thorough understanding of Global CMC drug development, strong management skills, financial & research management practices and long term planning skills.

Excellent knowledge of various international regulatory and GMP requirements.

Must be goal oriented, able to work within a team environment, self-motivated and understand the business needs to meet timelines.

Good verbal, written communication skills and the ability to interface with multiple areas within the organization is essential.

Previous related work experience in formulation/process and/or analytical service groups is preferred

Previous experience in supervising people is preferred.​

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.​

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

Seniority
Associate Director
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Waltham, MA
Employment type
Full-time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 857 comparable Associate Director Manufacturing & CMC roles across 113 biopharma companies.

857Comparable roles tracked
787Currently active
113Companies hiring similar roles
40Countries represented

Salary context

248 of 857 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.

This roleSubject $141,500/yr – $268,500/yr
Lowest disclosed · Senior Technician Calibration - Maintenance · Mylan Technologies, Inc. $37,000/yr – $80,000/yr
Highest disclosed · Associate Director / Director - Biologics Drug Product Development · AbbVie $160,500/yr – $305,000/yr
Peer group range $58,500 – $232,750 (median $155,000)

Where these roles are based

Top locations among the 857 comparable roles

United States467
India81
Ireland42
China26
Japan24
Netherlands22

+ 34 more countries

Seniority mix

857 of 857 peers have a known seniority level

Senior403
Manager351
Associate Director103

Therapeutic area mix

6 of 857 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease3
Dermatology & Aesthetics1
Immunology1
Vaccines & Infectious Disease1

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.

60%similar
AbbVie North Chicago, IL Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Amgen Inc. Remote, United States Associate Director
Same function Same seniority Same country
60%similar
Lilly Lebanon, Indiana, United States of America Associate Director
Same function Same seniority Same country
60%similar
Merck Wilmington, Delaware, United States Associate Director
Same function Same seniority Same country
60%similar
AbbVie Associate Director
Same function Same seniority Same country

Open in 2 locations

North Chicago, United StatesWorcester, United States

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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.

60%
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Function Therapeutic area Seniority Country
60%
Associate Director – Biologics Process Engineering, Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Associate Director
Function Therapeutic area Seniority Country
60%
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AbbVie · Worcester, MA · Associate Director
Function Therapeutic area Seniority Country
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Associate Director, Supply Chain
AstraZeneca · Gaithersburg, Maryland, United States of America · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.