Biotech Jobs at AbbVie with Visa Sponsorship
AbbVie's biotech roles span drug discovery, process development, and translational research across therapeutic areas including oncology, immunology, and neuroscience. The company has an established infrastructure for sponsoring international talent, making it a realistic target for scientists and researchers who need work authorization.
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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 80+ Biotech at AbbVie jobs
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Get Access To All JobsTips for Finding Biotech Jobs at AbbVie Jobs
Align Your Degree to AbbVie's Therapeutic Focus
AbbVie's biotech hiring centers on oncology, immunology, and neuroscience pipelines. Frame your academic credentials and research experience around these areas so your H-1B specialty occupation case maps cleanly to the role's degree requirements.
Use Migrate Mate to Filter AbbVie Biotech Openings
Not every AbbVie posting is open to sponsorship. Use Migrate Mate to surface biotech roles at AbbVie that are verified for visa sponsorship, so you're only investing time in applications where your visa type is actually supported.
Prepare for a Technical Interview Structure
AbbVie's biotech screening typically includes scientific depth questions on assay development, cell biology, or molecular techniques depending on the function. Arriving with peer-reviewed publications or documented lab contributions strengthens both your interview and your future H-1B petition.
Understand How AbbVie Handles the H-1B Cap Window
H-1B registrations open in March for an October 1 start date. If you receive an offer outside that window, ask your recruiter whether AbbVie can structure your start date around the next cap cycle or whether a cap-exempt arrangement applies to your role.
Biotech at AbbVie jobs are hiring across the US. Find yours.
Find Biotech at AbbVie JobsFrequently Asked Questions
Does AbbVie sponsor H-1B visas for Biotechs?
Yes, AbbVie sponsors H-1B visas for biotech roles. The company has an established immigration program and works with legal counsel to file petitions for qualifying positions in areas like process development, analytical sciences, and research. Roles must meet USCIS specialty occupation standards, which for biotech typically requires a bachelor's degree or higher in a directly related field such as biochemistry, molecular biology, or chemical engineering.
How do I apply for Biotech jobs at AbbVie?
Applications go through AbbVie's careers portal, where you can filter by function and location. For international applicants, Migrate Mate surfaces AbbVie's biotech openings that are open to visa sponsorship, helping you avoid roles that list sponsorship as unavailable. Tailor your resume to the specific therapeutic area and technical skills in the job description, as AbbVie's biotech teams hire for precise scientific competencies rather than general biology backgrounds.
Which visa types does AbbVie commonly use for Biotech roles?
AbbVie sponsors a range of visa types for biotech positions, including H-1B, H-1B1, E-3, TN, J-1, and F-1 OPT and CPT for students and recent graduates. For longer-term employment, the company also supports EB-2 and EB-3 Green Card sponsorship. The appropriate visa depends on your nationality, degree level, and the nature of the role.
What qualifications does AbbVie expect for Biotech positions?
Most biotech roles at AbbVie require a bachelor's, master's, or doctoral degree in a life sciences field, with the level depending on the seniority of the position. Laboratory-focused roles typically expect hands-on experience with relevant techniques such as cell culture, protein expression, flow cytometry, or CRISPR. Research scientist and associate scientist positions often prefer candidates with published work or documented experience in AbbVie's core therapeutic areas.
How do I time my application around the H-1B filing process?
The H-1B cap registration window opens in March, and approved petitions take effect October 1. If you're targeting a full-time AbbVie biotech role, aim to have an offer in hand by February so your employer can register during the annual lottery. If you're on F-1 OPT, your 60-day grace period after program end does not count as authorized employment, so plan your timeline around your OPT expiration date and the next available cap cycle.
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