Biotech & Pharma Jobs in Ohio with F-1 OPT Sponsorship
F-1 OPT biotech and pharma sponsorship jobs in Ohio are concentrated around Columbus, Cleveland, and Cincinnati, where employers like Battelle, Cardinal Health, Procter and Gamble, and the Cleveland Clinic research network actively hire international talent. Ohio's life sciences sector spans drug development, medical devices, and contract research, offering OPT-eligible graduates strong opportunities across research, regulatory, and quality 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 771+ 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 and pharma companies sponsor F-1 OPT visas in Ohio?
Ohio-based employers with documented histories of hiring F-1 OPT workers in life sciences include Battelle Memorial Institute in Columbus, Cardinal Health, Procter and Gamble in Cincinnati, and Lubrizol. Contract research organizations operating in the state, such as Covance and Syneos Health, also appear in DOL disclosure data as OPT sponsors. Sponsorship availability varies by role, department, and headcount at any given time, so confirming with each employer directly is important.
Which cities in Ohio have the most biotech and pharma F-1 OPT sponsorship jobs?
Columbus is Ohio's largest concentration of life sciences employment, anchored by Battelle, The Ohio State University Wexner Medical Center, and a growing cluster of biotech startups. Cleveland follows closely, driven by Cleveland Clinic's research operations and Case Western Reserve University's commercialization ecosystem. Cincinnati hosts Procter and Gamble's health sciences division along with several pharmaceutical manufacturing facilities. All three metros have active OPT hiring activity, though Columbus tends to post the highest volume of entry-level research roles.
What types of biotech and pharma roles typically qualify for F-1 OPT sponsorship in Ohio?
Roles that commonly appear in OPT hiring data for Ohio's biotech and pharma sector include research associate, analytical chemist, regulatory affairs coordinator, quality assurance specialist, bioinformatics analyst, and clinical data associate. These positions generally require a bachelor's or advanced degree in biology, chemistry, pharmaceutical sciences, or a related STEM field. OPT authorization must be directly related to your degree program, so the field of your degree needs to align with the role's core responsibilities.
How do I find biotech and pharma F-1 OPT sponsorship jobs in Ohio?
Migrate Mate lets you filter specifically for biotech and pharma employers in Ohio that have sponsored F-1 OPT workers, saving you from manually screening hundreds of postings. Because OPT sponsorship willingness is rarely advertised in job descriptions, using a platform built around verified sponsorship data is significantly more efficient. You can filter by city, role type, and industry on Migrate Mate to surface relevant Ohio openings and apply directly.
Are there any Ohio-specific considerations for F-1 OPT sponsorship in biotech and pharma?
Ohio has no state-level visa or work authorization requirements beyond federal F-1 OPT rules, but a few industry-specific factors matter. Many pharma manufacturing and quality roles require background checks or security clearances that can add processing time. Contract research organizations in Ohio frequently hire on project timelines, which may affect whether they can accommodate OPT's 12-month or 24-month STEM extension window. Verifying that your role and employer qualify for the STEM OPT extension before accepting an offer is worth confirming with your DSO.
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