Biotech & Pharma Jobs in Ohio with H-1B Sponsorship
H-1B visa sponsorship jobs in Ohio's biotech and pharma sector are concentrated around Columbus, Cleveland, and Cincinnati, where employers like Battelle, Cardinal Health, and Procter & Gamble have active research and development operations. Ohio's life sciences ecosystem, anchored by major research universities and a growing biopharma manufacturing base, supports steady demand for international talent in scientific and technical roles.
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INTRODUCTION
A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
ROLE AND RESPONSIBILITIES
This position will require working in various Controlled/Non-Classified areas. The Packaging Technician performs a variety of manufacturing tasks (operates equipment, performs in-process monitoring, line clearances, cosmetic inspection, cleaning and completes batch record entries) and supports improvement activities (5S, participate in problem-solving and Kaizen events, manual data collection) to achieve a prescribed level of purity, quality, and consistency in product and work output in accordance with cGMPs. Night shift position working 6pm- 6:30am. 2 days on, 2 days off, 3 days on, 3 days off then the rotation starts over again.
-
Perform the duties of operating assigned machinery consisting of servicing machines with materials, monitoring equipment status, reintroduction of materials, manually palletizing finished materials, and assuring a smooth flow of product.
-
Be able to start-up machinery including equipment set-up, perform recipe selection and data entry on manufacturing computerized system (SCADA and HMI), make minor adjustments, and perform critical sensor challenges.
-
Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material.
-
Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) as the need arises to safely move, store or deliver material to the proper location.
-
Perform visual quality inspection and sampling of in-process materials. Promptly escalate concerns to Lead and Process Facilitator as needed.
-
Perform minor troubleshooting including clearing minor jams and identifying equipment defects.
-
Work collaboratively with technical resources to resolve equipment issues as needed.
-
Perform inventory control and reconciliation activities, which may require the use of SAP and WES in a limited role.
-
Perform cleaning, housekeeping and line clearance activities for assigned areas to maintain a cGMP environment. This includes assembling, disassembling, and sanitizing various packaging equipment.
-
Perform batch record and GMP documentation entries. Perform mathematical computation as needed.
-
Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, LOTO, human safety, material handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.
-
Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety and quality procedures.
-
Support lean activities and process improvement work such as performing 5S in the work area, participating in problem-solving, and manual tracking of performance data for OEE and process improvement analysis.
-
Act as a certified OJT trainer on the team on assigned equipment and process tasks. Train and conduct evaluations on other team members for training qualifications.
-
Review process documents such as operational SOPs, forms, and batch records for accuracy.
-
Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.
-
Execute protocols as required as a part of equipment qualification and process validation work.
-
Be flexible and support other work areas within the Manufacturing Team as needed.
-
Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.
-
Acquire and maintain all required certifications and qualifications for the assigned work area.
-
Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Process Execution Team.
-
Ability to work effectively in a team environment.
-
Candidate should possess the ability to work in and adapt to a changing/demanding environment.
-
Some overtime may be required with minimal advance notice to support business needs.
MINIMUM REQUIREMENTS
-
Experience in a pharmaceutical or cGMP regulated environment.
-
Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language.
-
Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations.
PREFERRED BACKGROUND
-
High school graduate, vocational school graduate or equivalent.
-
Working knowledge of Microsoft applications and SAP.
-
Prior production experience.
-
Experience working in a LEAN manufacturing environment.
-
Knowledge of cGMPs and FDA policies/procedures.
Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $32.00 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.

INTRODUCTION
A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
ROLE AND RESPONSIBILITIES
This position will require working in various Controlled/Non-Classified areas. The Packaging Technician performs a variety of manufacturing tasks (operates equipment, performs in-process monitoring, line clearances, cosmetic inspection, cleaning and completes batch record entries) and supports improvement activities (5S, participate in problem-solving and Kaizen events, manual data collection) to achieve a prescribed level of purity, quality, and consistency in product and work output in accordance with cGMPs. Night shift position working 6pm- 6:30am. 2 days on, 2 days off, 3 days on, 3 days off then the rotation starts over again.
-
Perform the duties of operating assigned machinery consisting of servicing machines with materials, monitoring equipment status, reintroduction of materials, manually palletizing finished materials, and assuring a smooth flow of product.
-
Be able to start-up machinery including equipment set-up, perform recipe selection and data entry on manufacturing computerized system (SCADA and HMI), make minor adjustments, and perform critical sensor challenges.
-
Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material.
-
Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) as the need arises to safely move, store or deliver material to the proper location.
-
Perform visual quality inspection and sampling of in-process materials. Promptly escalate concerns to Lead and Process Facilitator as needed.
-
Perform minor troubleshooting including clearing minor jams and identifying equipment defects.
-
Work collaboratively with technical resources to resolve equipment issues as needed.
-
Perform inventory control and reconciliation activities, which may require the use of SAP and WES in a limited role.
-
Perform cleaning, housekeeping and line clearance activities for assigned areas to maintain a cGMP environment. This includes assembling, disassembling, and sanitizing various packaging equipment.
-
Perform batch record and GMP documentation entries. Perform mathematical computation as needed.
-
Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, LOTO, human safety, material handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.
-
Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety and quality procedures.
-
Support lean activities and process improvement work such as performing 5S in the work area, participating in problem-solving, and manual tracking of performance data for OEE and process improvement analysis.
-
Act as a certified OJT trainer on the team on assigned equipment and process tasks. Train and conduct evaluations on other team members for training qualifications.
-
Review process documents such as operational SOPs, forms, and batch records for accuracy.
-
Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.
-
Execute protocols as required as a part of equipment qualification and process validation work.
-
Be flexible and support other work areas within the Manufacturing Team as needed.
-
Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.
-
Acquire and maintain all required certifications and qualifications for the assigned work area.
-
Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Process Execution Team.
-
Ability to work effectively in a team environment.
-
Candidate should possess the ability to work in and adapt to a changing/demanding environment.
-
Some overtime may be required with minimal advance notice to support business needs.
MINIMUM REQUIREMENTS
-
Experience in a pharmaceutical or cGMP regulated environment.
-
Must have the ability to effectively understand, read, write, communicate, and follow instructions in the English language.
-
Good attention to detail is required. Individual must be capable of keeping accurate records and performing mathematical calculations.
PREFERRED BACKGROUND
-
High school graduate, vocational school graduate or equivalent.
-
Working knowledge of Microsoft applications and SAP.
-
Prior production experience.
-
Experience working in a LEAN manufacturing environment.
-
Knowledge of cGMPs and FDA policies/procedures.
Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50 - $32.00 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.
Job Roles in Biotech & Pharma in Ohio
See all 942+ Biotech & Pharma Ohio jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biotech & Pharma Ohio roles.
Get Access To All JobsFrequently Asked Questions
Which biotech & pharma companies sponsor H-1B visas in Ohio?
Several large employers in Ohio have documented H-1B sponsorship histories in the biotech and pharma space. Cardinal Health, headquartered in Dublin, regularly files for roles in regulatory affairs, data science, and supply chain. Battelle Memorial Institute in Columbus sponsors researchers and life sciences professionals. Procter & Gamble in Cincinnati files petitions for scientific and R&D positions. Smaller CROs and medical device firms across the state also appear in DOL disclosure data.
Which cities in Ohio have the most biotech & pharma H-1B sponsorship jobs?
Columbus is Ohio's largest hub for biotech and pharma H-1B roles, driven by Battelle, Cardinal Health's operations, and proximity to Ohio State University's research programs. Cincinnati follows closely, with Procter & Gamble and a cluster of pharmaceutical manufacturing firms. Cleveland supports life sciences hiring through its medical device sector and institutions affiliated with the Cleveland Clinic. Smaller concentrations exist in Dayton and Toledo, particularly in manufacturing and quality assurance roles.
What types of biotech & pharma roles typically qualify for H-1B sponsorship in Ohio?
Roles that qualify for H-1B sponsorship in Ohio's biotech and pharma industry are those classified as specialty occupations, meaning they require at least a bachelor's degree in a specific field. Common qualifying positions include research scientists, biomedical engineers, regulatory affairs specialists, bioinformatics analysts, quality assurance managers, clinical research associates, and computational biologists. General laboratory technician roles or positions where any bachelor's degree is acceptable may not meet the specialty occupation standard without additional documentation.
How do I find biotech & pharma H-1B sponsorship jobs in Ohio?
Migrate Mate is built specifically for international job seekers and filters biotech and pharma listings in Ohio by H-1B sponsorship history, so you can focus on employers who have actually filed petitions rather than guessing. You can browse roles by city, job function, and employer, which is particularly useful in Ohio where sponsoring companies are spread across Columbus, Cincinnati, and Cleveland. Searching through Migrate Mate saves significant time compared to manually cross-referencing DOL disclosure data.
Are there any Ohio-specific considerations for H-1B sponsorship in biotech & pharma?
Ohio does not have state-level visa programs, so all H-1B sponsorship follows federal USCIS rules regardless of location. One practical consideration is that Ohio's biotech sector includes a significant number of contract research organizations and smaller startups, some of which may have less experience navigating H-1B petitions than larger pharmaceutical firms. Candidates evaluating smaller employers should confirm the company has existing immigration counsel and a track record of successful sponsorship before accepting an offer.
What is the prevailing wage for H-1B biotech & pharma jobs in Ohio?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.
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