Product Engineer Jobs at AbbVie with Visa Sponsorship
Product Engineer jobs at AbbVie support drug development, manufacturing systems, and process validation across its pharmaceutical pipeline. The company has a consistent track record of sponsoring work visas for this function, covering both temporary work authorization and longer-term permanent residency 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. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Batch Record Reviewer audits manufacturing and packaging batch records for accuracy and compliance to AbbVie policies and procedures and performs transactions in inventory systems to release the batch for further processing.
Responsibilities
- Review and audit the data and records generated by Manufacturing and Packaging Operations in the processing of a material or product batch
- Ensure any batch record errors are corrected, all batch record components are present, and exception documents are referenced and approved
- Ensure all in-process and release testing is complete and all Quality holds are released
- Interface with various electronic databases/systems to interpret data pertinent for release to specific countries
- Ensure batch records are retained and filed securely
- Ensure Quality goals are met and all practices and procedures comply with Company policies and applicable regulations
- Interact with other AbbVie departments, external customers, and regulatory agencies
- May release batch records in electronic systems according to global, local, customer, and regulatory requirements
BASIC QUALIFICATIONS
- Minimum High School graduate; Bachelor's or Associate's degree desired
- 2+ years of overall experience in Manufacturing, Quality or Engineering
- Minimum 5 years of experience in a manufacturing/finishing environment is desired
- Knowledge of GMP regulations and standards affecting pharmaceutical products
- Good analytical skills and attention to detail
- Good interpersonal relations / communications skills
- Good verbal and written communication skills
- Must be available to work daily overtime, including weekends, as needed
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 short-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
The Batch Record Reviewer audits manufacturing and packaging batch records for accuracy and compliance to AbbVie policies and procedures and performs transactions in inventory systems to release the batch for further processing.
Responsibilities
- Review and audit the data and records generated by Manufacturing and Packaging Operations in the processing of a material or product batch
- Ensure any batch record errors are corrected, all batch record components are present, and exception documents are referenced and approved
- Ensure all in-process and release testing is complete and all Quality holds are released
- Interface with various electronic databases/systems to interpret data pertinent for release to specific countries
- Ensure batch records are retained and filed securely
- Ensure Quality goals are met and all practices and procedures comply with Company policies and applicable regulations
- Interact with other AbbVie departments, external customers, and regulatory agencies
- May release batch records in electronic systems according to global, local, customer, and regulatory requirements
BASIC QUALIFICATIONS
- Minimum High School graduate; Bachelor's or Associate's degree desired
- 2+ years of overall experience in Manufacturing, Quality or Engineering
- Minimum 5 years of experience in a manufacturing/finishing environment is desired
- Knowledge of GMP regulations and standards affecting pharmaceutical products
- Good analytical skills and attention to detail
- Good interpersonal relations / communications skills
- Good verbal and written communication skills
- Must be available to work daily overtime, including weekends, as needed
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 short-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 Product Engineer Jobs at AbbVie
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Product Engineer Jobs at AbbVie.
Get Access To All JobsTips for Finding Product Engineer Jobs at AbbVie
Align Your Credentials to GMP Standards
AbbVie's Product Engineer roles sit inside a regulated manufacturing environment. Certifications or coursework in Good Manufacturing Practices, process validation, or FDA compliance make your application materially stronger before you submit a single form.
Target Roles Tied to Active Product Lines
AbbVie's engineering headcount follows its pipeline. Product Engineer openings are concentrated around facilities supporting biologics and immunology products, so filtering your search by those therapeutic areas surfaces the postings with the most active hiring mandates.
Clarify Sponsorship Type Before Accepting an Offer
AbbVie sponsors multiple visa categories for Product Engineers. Before you sign, confirm whether the offer covers H-1B, E-3, or TN, and ask whether the employer will also support a future Green Card petition through PERM or an EB-2 self-petition.
Prepare for a Technical and Regulatory Interview Track
AbbVie's Product Engineer interviews typically cover both engineering fundamentals and regulatory knowledge. Preparing answers around process deviation handling, CAPA systems, and equipment qualification puts you ahead of candidates with only academic credentials.
Use Migrate Mate to Filter Verified Sponsorship Postings
Browsing open Product Engineer roles at AbbVie is faster when the job board already screens for visa sponsorship history. Migrate Mate filters postings specifically for employers with a documented track record, so you spend time on applications that are actually viable for your status.
Time Your H-1B Filing Around the April Cap Season
If you need an H-1B, your employer must register you in USCIS's lottery by mid-March for an October 1 start. Confirm AbbVie has submitted your offer paperwork well before that window closes, particularly if your OPT or current status expires in the same calendar year.
Frequently Asked Questions
Does AbbVie sponsor H-1B visas for Product Engineers?
Yes, AbbVie sponsors H-1B visas for Product Engineer roles. The company participates in the annual H-1B cap lottery and also files cap-exempt petitions where applicable. If you are already on H-1B with another employer, AbbVie can file an H-1B transfer so you maintain work authorization without waiting for a new cap cycle.
Which visa types does AbbVie commonly sponsor for Product Engineers?
AbbVie sponsors H-1B, H-1B1 visa, E-3 visa, TN visa, F-1 OPT, and F-1 CPT for Product Engineers, along with Green Card pathways through EB-2 and EB-3 PERM. Australian citizens should ask specifically about the E-3 visa, which has no lottery and renews in two-year increments. Canadian and Mexican nationals with qualifying engineering degrees may qualify for TN visa status, which can be arranged at the border without USCIS filing.
What qualifications does AbbVie expect for a Product Engineer role?
Most Product Engineer postings at AbbVie require a bachelor's degree in chemical, mechanical, or biomedical engineering, or a closely related field. Hands-on experience with process validation, equipment qualification, or pharmaceutical manufacturing is weighted heavily. Familiarity with FDA regulations and Good Manufacturing Practices is treated as a baseline expectation, not a differentiator, at the mid-level and senior levels.
How do I apply for Product Engineer jobs at AbbVie?
You can browse open Product Engineer positions at AbbVie directly through Migrate Mate, which filters for roles where visa sponsorship has been documented. Apply through AbbVie's careers portal with a resume that explicitly addresses process validation experience and regulatory knowledge. Tailoring your application to the specific product area listed in the posting improves your chances of clearing the initial screening.
How do I plan my timeline if AbbVie needs to file an H-1B for me?
The H-1B cap lottery registration opens in early March each year. If selected, your petition is filed by April 1 for an October 1 start date. That gap means you need OPT, a grace period, or another valid status to bridge the wait. If your OPT expires before October, confirm with AbbVie whether cap-gap protection applies or whether an alternative visa category can cover the interim period.