QA Director
Location: Worcester
Posted on: June 23, 2025
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Job Description:
Company Description 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 immunology, oncology, neuroscience, and eye care.
For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on X , Facebook , Instagram ,
YouTube , LinkedIn and Tik Tok . Job Description Purpose The
Director of Quality Control , Quality Assurance, Product Release,
or Tissue Services is a key member of the quality leadership team
and reports directly to the Site Head of Quality. This role is
responsible for providing strategic leadership, appropriate
staffing, and sustaining a quality culture, in line with the
organizations global strategy and the site's goals and
objectives.The incumbent is responsible for strategic direction of
one or more of the following functions/teams: Supplier
Controls/Incoming Material Inspection, Incoming Tissue Inspection,
Final Product Packaging Inspection, Product Release, Donor
Eligibility and Release, Product Change Control,
Facility/Utility/Equipment Qualification. Responsibilities
Establish a Quality Control Strategy for all applicable products
and implement appropriate processes and staffing for strategy
achievement, which includes the following areas: Incoming material
inspection and release, lot review and release, final packaging
inspection, Donor review process Carry out duties as a leader
within the quality organization to ensure quality requirements are
met. Act as delegate; Management with Executive Responsibility,
Management Representative, or Person(s) Responsible for Regulatory
Compliance: The conformity of the product/device is checked in
accordance with the quality management system before release and
compliance of product/device used for clinical investigation is
documented. Monitor and implement processes to ensure compliance
with Regulations and guidelines including, but not limited to, FDA
21CFR1271, 210, 211, 806, and 820, ISO9001 and 13485, Canadian
regulations, Tissue Banking Standards, and Global and State
regulations, Benchmark and leverage best practices in the industry
and with key corporate partners. Assess Team performance using
metrics and implement improvement initiatives where gaps or trends
are identified. Act as a leader and role model to all Quality
employees Partner with manufacturing to achieve product supply
goals while ensuring compliance with quality requirements and
applicable regulations. Participate in market demand forecasting
and align resources to meet demand Ensures project deadlines and
performance standards are established and met Ensures the creation
of goals and objectives in alignment with the overall strategy
Qualifications Bachelor's degree required in Business, Biology,
Engineering, or related scientific field from an accredited college
or university Minimum 15 years of relevant experience in
Quality/Regulatory in pharma, biologics, medical device, or
relevant regulated industry.Additional experience outside
Quality/Regulatory functions desired. Demonstrated knowledge in
Quality Systems, Quality Operations practices, and procedures.
Demonstrated people management skills including leadership,
strategic planning, delegation, and follow up along with
recruiting, developing, and retaining key talent Knowledge of risk
analysis tools and statistical methodology Ability to gown and
enter cleanroom processing environments and work within an office
setting Additional Information Applicable only to applicants
applying to a position in any location with pay disclosure
requirements under state orlocal law: The compensation range
described below is the range of possible base pay compensation that
the Companybelieves ingood faith it will pay for this role at the
timeof this posting based on the job grade for this
position.Individualcompensation paid within this range will depend
on many factors including geographic location, andwemay
ultimatelypay more or less than the posted range. This range may be
modified in thefuture.Salary: $156,000 - $296,500 We offer a
comprehensive package of benefits including paid time off
(vacation, holidays, sick),medical/dental/visioninsurance and
401(k) to eligibleemployees. This job is eligible to participate in
our short-term incentiveprograms. This job is eligible to
participate in our long-term incentiveprograms Note: No amount of
payis considered to bewages or compensation until such amount is
earned, vested, anddeterminable.The amount and availability of any
bonus,commission, incentive, benefits, or any other form
ofcompensation and benefitsthat are allocable to a particular
employee remains in the Company's sole andabsolutediscretion unless
and until paid andmay be modified at the Companys sole and absolute
discretion, consistent withapplicable 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
Keywords: , Marthas Vineyard , QA Director, Science, Research & Development , Worcester, Massachusetts