Program Manager Jobs at AbbVie with Visa Sponsorship
AbbVie hires Program Managers across drug development, clinical operations, and commercial functions, with roles spanning therapeutic areas from immunology to oncology. The company has a consistent track record of sponsoring work visas for qualified program management professionals, making it a realistic target for international candidates.
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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. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Purpose:
The Program Manager is an experienced leader responsible for managing large global projects across disciplines and multiple manufacturing locations. This person has previous project management experience and is working on expanding into managing various projects. This individual provides leadership and coordinated project management for all manufacturing and/or technical activities needed to ensure successful tech transfer and commercialization of the assigned products by integrating the efforts of R&D, S&T, Quality, Supply Chain, Regulatory. After product launch, this individual is responsible for managing the capacity strategy for the product, assurance of supply programs and cost reduction initiatives across the network.
Responsibilities
- Responsible for providing technical input, leading to shape the overall strategies for the front end planning, due diligence and technical feasibility assessments for potential new product introductions.
- Implement site transfers, new indications, new presentations and lifecycle projects for on market programs on time and within budget.
- Proactively identify and drive technical and project plan related issues to closure by working with all relevant functional lines and effectively troubleshooting and driving decisions.
- Manage multiple projects concurrently, operating with minimal supervision.
- Understand project drivers, requirements, scenarios and options. Proactively drive development of contingency and/or risk mitigation plans.
- Manage competing timelines and make difficult decisions regarding priorities among projects.
- Effectively communicate and present project status to Operations senior management and stakeholders. Accountable for setting program and project plans, including timelines and expenses, that meet business and organizational objectives and ensuring those plans are achieved.
- Define budget requirements and report monthly actuals, LBE, and Plan/LRP schedules per financial schedule.
Qualifications
- Bachelor’s Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence.
- 10+ years of combined experience in positions related to process development, project management, engineering/process support and manufacturing.
- Must have strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations.
- Must have demonstrated organizational and planning skills, excellent verbal and written communication skills.
- Must have demonstrated strong project management skills with successful delivery of projects.
- Must be able to effectively facilitate the resolution of complex scientific, technical, analytical and business issues across functional lines.
- Plant experience a must.
- PMP certification a plus.
- Proficiency in multiple languages a plus.
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
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
Purpose:
The Program Manager is an experienced leader responsible for managing large global projects across disciplines and multiple manufacturing locations. This person has previous project management experience and is working on expanding into managing various projects. This individual provides leadership and coordinated project management for all manufacturing and/or technical activities needed to ensure successful tech transfer and commercialization of the assigned products by integrating the efforts of R&D, S&T, Quality, Supply Chain, Regulatory. After product launch, this individual is responsible for managing the capacity strategy for the product, assurance of supply programs and cost reduction initiatives across the network.
Responsibilities
- Responsible for providing technical input, leading to shape the overall strategies for the front end planning, due diligence and technical feasibility assessments for potential new product introductions.
- Implement site transfers, new indications, new presentations and lifecycle projects for on market programs on time and within budget.
- Proactively identify and drive technical and project plan related issues to closure by working with all relevant functional lines and effectively troubleshooting and driving decisions.
- Manage multiple projects concurrently, operating with minimal supervision.
- Understand project drivers, requirements, scenarios and options. Proactively drive development of contingency and/or risk mitigation plans.
- Manage competing timelines and make difficult decisions regarding priorities among projects.
- Effectively communicate and present project status to Operations senior management and stakeholders. Accountable for setting program and project plans, including timelines and expenses, that meet business and organizational objectives and ensuring those plans are achieved.
- Define budget requirements and report monthly actuals, LBE, and Plan/LRP schedules per financial schedule.
Qualifications
- Bachelor’s Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence.
- 10+ years of combined experience in positions related to process development, project management, engineering/process support and manufacturing.
- Must have strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations.
- Must have demonstrated organizational and planning skills, excellent verbal and written communication skills.
- Must have demonstrated strong project management skills with successful delivery of projects.
- Must be able to effectively facilitate the resolution of complex scientific, technical, analytical and business issues across functional lines.
- Plant experience a must.
- PMP certification a plus.
- Proficiency in multiple languages a plus.
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
See all 91+ Program Manager at AbbVie jobs
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Get Access To All JobsTips for Finding Program Manager Jobs at AbbVie Jobs
Align your credentials to biopharma standards
AbbVie's Program Manager roles in clinical or regulatory functions often require PMP certification or an advanced degree in life sciences. Confirm your credentials map to the specific team you're targeting before applying.
Target therapeutic area teams strategically
AbbVie concentrates program management hiring around immunology, oncology, and neuroscience pipelines. Searching by therapeutic area rather than just job title surfaces roles where cross-functional coordination experience, not just project management, is the real differentiator.
Understand the LCA filing requirement
Before AbbVie can petition USCIS for your H-1B, the company must file a Labor Condition Application with the DOL certifying your offered wage meets prevailing levels. Delays here can push your start date, so ask your recruiter about the LCA timeline during offer negotiation.
Use Migrate Mate to filter verified sponsoring roles
Program Manager openings at large biopharma companies aren't always tagged with sponsorship eligibility on general job boards. Use Migrate Mate to filter AbbVie listings to roles where visa sponsorship has been confirmed, saving time on applications that won't move forward.
Account for PERM timing if pursuing permanent residency
If you're targeting a Green Card through AbbVie's EB-2 or EB-3 pathway, PERM labor certification can take 12 to 18 months before USCIS even receives your I-140. Discuss the company's green card policy during the offer stage, not after you've started.
Program Manager at AbbVie jobs are hiring across the US. Find yours.
Find Program Manager at AbbVie JobsFrequently Asked Questions
Does AbbVie sponsor H-1B visas for Program Managers?
Yes, AbbVie sponsors H-1B visas for Program Manager roles. Program management positions in drug development, clinical operations, and commercial functions typically qualify as specialty occupations under USCIS standards, requiring a bachelor's degree or higher in a relevant field. AbbVie handles the petition process through its legal team, and sponsorship is generally initiated after a formal offer is extended.
Which visa types does AbbVie commonly sponsor for Program Manager roles?
AbbVie sponsors several visa categories for Program Managers, including H-1B, H-1B1, E-3, TN, J-1, and F-1 OPT and CPT. The right category depends on your nationality and current status. Australian citizens are eligible for E-3, Canadian and Mexican nationals can pursue TN, and current F-1 students often start on OPT before transitioning to employer-sponsored status.
What qualifications does AbbVie expect for Program Manager roles?
Most Program Manager roles at AbbVie require a bachelor's degree in life sciences, engineering, business, or a related field, with several years of relevant program or project management experience. Roles tied to clinical development or regulatory affairs often prefer candidates with direct biopharma backgrounds. PMP certification strengthens applications for roles with cross-functional or enterprise-level scope.
How do I apply for Program Manager jobs at AbbVie?
You can search and apply for Program Manager roles directly through AbbVie's careers site or use Migrate Mate to browse verified AbbVie openings filtered by visa sponsorship eligibility. When applying, tailor your resume to the specific therapeutic area or function the role supports. After submitting, initial screening typically happens within two to three weeks for active requisitions.
How do I understand the timeline for H-1B sponsorship at AbbVie?
If you need cap-subject H-1B sponsorship, AbbVie must register you in USCIS's lottery in March for an October 1 start date. If selected, the petition window opens April 1. For candidates already on H-1B with another employer, AbbVie can file an H-1B transfer and you can start once USCIS issues a receipt notice, without waiting for October 1.
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