Product Director Jobs at AbbVie with Visa Sponsorship
AbbVie hires Product Directors to lead cross-functional teams across its pharmaceutical and biologics portfolio, from early-stage pipeline assets to commercial launches. The company has a consistent track record of sponsoring work visas for this function, supporting candidates through both nonimmigrant and immigrant visa pathways.
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Get Access To All JobsCompany 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.
Job Description
Overview:
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Associate Director, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product development. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.
Responsibilities:
- Serve as single point of contact for programs developed in collaboration with external partners.
- Develop and execute robust drug product development strategies for external programs.
- Serve as a drug product team leader for one or more projects and represents Bio DPD in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.
- Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.
- Support due diligence for business development opportunities.
Qualifications
- Bachelors, Masters, or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related disciplines with 16+ (Bachelors), 14+ (Masters), or 8+ (PhD) years of relevant industry experience
- Proven ability to solve critical scientific problems
- Strong experience working with external partners, contract research organizations and third-party manufacturers
- Strong experience with biologics (proteins, conjugates, peptides and/or neurotoxins), parenteral synthetic molecules and/or genetic medicine (AAV, LNPs, cell therapy) drug product formulation and process development, and tech transfer
- Extensive experience with sterile manufacturing unit operations (freeze-thaw, compounding, mixing, filtration and filling) development and transfer
- Experience as CMC cross-functional matrix team leader with strong ability to influence without authority
- Hands-on experience with authoring regulatory filings for biologics and sterile parenteral products
- Understanding of relevant cGMP and regulatory guidance for biologics and sterile parenteral products
- Experience with quality risk management and control strategies for biologics and sterile parenteral products
Key Competencies:
- Deep scientific knowledge and significant hands-on experience with biologics and parenteral drug product development
- Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement
- Builds strong relationships with peers and cross-functional partners to enable higher performance
- Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance
- Raises the bar and is never satisfied with the status quo
- Creates a learning environment, open to suggestions and experimentation for improvement
- Embraces the ideas of others, nurtures innovation and manages innovation to reality
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 the AbbVie website. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more.
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.
Job Description
Overview:
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Associate Director, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product development. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.
Responsibilities:
- Serve as single point of contact for programs developed in collaboration with external partners.
- Develop and execute robust drug product development strategies for external programs.
- Serve as a drug product team leader for one or more projects and represents Bio DPD in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.
- Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.
- Support due diligence for business development opportunities.
Qualifications
- Bachelors, Masters, or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related disciplines with 16+ (Bachelors), 14+ (Masters), or 8+ (PhD) years of relevant industry experience
- Proven ability to solve critical scientific problems
- Strong experience working with external partners, contract research organizations and third-party manufacturers
- Strong experience with biologics (proteins, conjugates, peptides and/or neurotoxins), parenteral synthetic molecules and/or genetic medicine (AAV, LNPs, cell therapy) drug product formulation and process development, and tech transfer
- Extensive experience with sterile manufacturing unit operations (freeze-thaw, compounding, mixing, filtration and filling) development and transfer
- Experience as CMC cross-functional matrix team leader with strong ability to influence without authority
- Hands-on experience with authoring regulatory filings for biologics and sterile parenteral products
- Understanding of relevant cGMP and regulatory guidance for biologics and sterile parenteral products
- Experience with quality risk management and control strategies for biologics and sterile parenteral products
Key Competencies:
- Deep scientific knowledge and significant hands-on experience with biologics and parenteral drug product development
- Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement
- Builds strong relationships with peers and cross-functional partners to enable higher performance
- Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance
- Raises the bar and is never satisfied with the status quo
- Creates a learning environment, open to suggestions and experimentation for improvement
- Embraces the ideas of others, nurtures innovation and manages innovation to reality
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 the AbbVie website. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more.
See all 26+ Product Director at AbbVie jobs
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Get Access To All JobsTips for Finding Product Director Jobs at AbbVie Jobs
Align your portfolio to AbbVie's therapeutic areas
AbbVie's Product Director roles cluster around immunology, oncology, neuroscience, and aesthetics. Tailor your resume and cover letter to show direct experience in at least one of these franchises, not general pharma product management.
Prepare a specialty occupation narrative early
USCIS requires H-1B petitions to demonstrate the role qualifies as a specialty occupation. For Product Director positions, document how your degree in life sciences, pharmacy, or a related field directly applies to the specific responsibilities AbbVie lists in the job description.
Target roles tied to AbbVie's commercial pipeline launches
Product Directors with launch experience on biologics or specialty drugs are prioritized during hiring cycles tied to new FDA approvals. Monitoring AbbVie's pipeline milestones helps you time your application when headcount demand is highest and sponsorship decisions move faster.
Use Migrate Mate to filter AbbVie's open Product Director roles
Browsing open roles by visa type narrows your search to positions where sponsorship is confirmed. Use Migrate Mate to filter AbbVie's Product Director listings by the visa category you need so you're only spending time on opportunities that are already a match.
Understand PERM timing if you need a Green Card
AbbVie supports EB-2 and EB-3 immigrant visa sponsorship, but PERM labor certification through DOL typically takes 12 to 18 months before an I-140 is filed. Factor this into your planning if you're approaching the end of your H-1B validity or OPT period.
Product Director at AbbVie jobs are hiring across the US. Find yours.
Find Product Director at AbbVie JobsFrequently Asked Questions
Does AbbVie sponsor H-1B visas for Product Directors?
Yes, AbbVie sponsors H-1B visas for Product Director roles. The company has an established process for filing H-1B petitions through its internal immigration team, which works alongside outside counsel. Product Directors typically qualify under the specialty occupation standard given the degree requirements in life sciences, business, or a related field that AbbVie specifies for these positions.
Which visa types does AbbVie commonly sponsor for Product Director roles?
AbbVie sponsors a range of visa categories for Product Directors, including H-1B, H-1B1 for Chilean and Singaporean nationals, E-3 for Australian citizens, TN for Canadian and Mexican professionals, F-1 OPT and CPT for recent graduates, and J-1 for exchange visitors. For candidates pursuing permanent residence, AbbVie also supports EB-2 and EB-3 Green Card sponsorship through the PERM labor certification process.
What qualifications does AbbVie expect for a Product Director role?
AbbVie's Product Director roles typically require a bachelor's degree in a life sciences or business-related field, with an advanced degree preferred, and substantial experience in pharmaceutical or biotech product management. Hands-on experience leading a product through launch, cross-functional team leadership, and familiarity with regulatory and market access processes in AbbVie's core therapeutic areas strengthen your candidacy significantly.
How do I apply for Product Director jobs at AbbVie?
You can search and apply for Product Director positions directly through AbbVie's careers site or browse verified sponsorship-confirmed listings on Migrate Mate, which filters roles by visa type so you can confirm sponsorship eligibility before applying. Applications typically require a resume tailored to the specific therapeutic area and pipeline stage listed in the job description, along with responses to AbbVie's standard screening questions about work authorization.
How do I plan my timeline around AbbVie's H-1B sponsorship process?
If you're on F-1 OPT, the H-1B cap lottery opens in March for an October 1 start date, so you and AbbVie need to align on timing well before that window. AbbVie's HR and immigration teams are experienced with this cycle. If you miss the lottery or aren't subject to the cap, options like cap-exempt filing or E-3 sponsorship may apply depending on your nationality and employment situation.
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