Biotech & Pharma STEM OPT Jobs in Georgia
Georgia's biotech and pharma sector, anchored by Atlanta's Midtown and Peachtree City corridor, employs F-1 STEM OPT holders across companies like Novelis, Inspire Brands' science divisions, and growing CROs near the CDC campus. Roles in bioinformatics, quality assurance, and process development routinely qualify, making Georgia a practical target for STEM OPT job seekers in life sciences.
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Get Access To All JobsAs an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees.
ROLE AND RESPONSIBILITIES
- Facilitates changes to existing production processes.
- Accountable for installation, commissioning, start-up of new equipment and changes to existing equipment.
- Assists with validation of new equipment and changes to existing equipment including document generation.
- Acts as change control owner for equipment and process improvement projects. Coordinate change control meetings.
- Assigns action items for change control.
- Accountable for change control action items and documentation. Documentation includes drawings, functional specifications, detailed design specifications, Turn-over-packages, material specifications, and other documentation as required.
- Supports troubleshooting product and equipment issues in production areas such as biomanufacturing, formulation and filling, lyophilization and packaging.
- Identifies improvements to manufacturing process. Improvements may include mechanical, automation, or workflow.
- Works with manufacturing and capital engineering on the development of future capital projects and on the development of requirements for the project.
- Responsible for User Requirement Specification development.
- Assists cross functional teams in the execution of small-scale capital projects up to around $500,000, process improvement projects, continuous improvement projects, and equipment improvement projects.
- On larger capital projects, the engineer will be responsible for ensuring process requirements are communicated and built into the equipment/system design. The engineer will develop specifications (user, functional, and detailed design) for equipment and automation of the equipment.
- Develops and maintains overall knowledge of facility processes and products.
- Provides training on process and/or equipment modifications as required for new or existing equipment/processes.
- Acts as Subject Matter Expert for production equipment and processes for Capital Engineering, Production, Business Process Science, Quality Assurance, and Maintenance.
BASIC QUALIFICATIONS
- Bachelor of Science Degree in Engineering from an accredited school with one to three (1-3) years applicable experience in a GMP environment or Bachelor´s degree with three to five (3-5) of engineering or scientific experience outside of a GMP environment.
- In lieu of years of experience, Master´s Degree in relevant field from an accredited school with one (1) year experience in a GMP environment or at least one (1) year of engineering or two (2) years of scientific experience outside of a GMP environment.
- At least one (1) year of experience leading projects preferable.
COMPETENCIES
- Effective verbal and written communication with all levels of corporate and local management and employees.
- Ability to plan, schedule, organize, prioritize, and coordinate project activities.
- Ability to understand and work within a regulated environment.
- Experience with GAMP Automation practices and documents preferred.
- Ability to function in a leadership role as well as in a team environment.
- Ability to manage multiple projects at one time.
SKILLS
- Analytical Thinking
- Data collection and analysis
- Communication
- Customer Focus
- Data-driven Decision Making
- Planning and Organizing
- Teamwork
- Conceptual / Analytical Thinking Scope
- Delivering Results
- Leadership
DESIRED SKILLS, EXPERIENCE AND ABILITIES
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim´s high regard for our employees.
ROLE AND RESPONSIBILITIES
- Facilitates changes to existing production processes.
- Accountable for installation, commissioning, start-up of new equipment and changes to existing equipment.
- Assists with validation of new equipment and changes to existing equipment including document generation.
- Acts as change control owner for equipment and process improvement projects. Coordinate change control meetings.
- Assigns action items for change control.
- Accountable for change control action items and documentation. Documentation includes drawings, functional specifications, detailed design specifications, Turn-over-packages, material specifications, and other documentation as required.
- Supports troubleshooting product and equipment issues in production areas such as biomanufacturing, formulation and filling, lyophilization and packaging.
- Identifies improvements to manufacturing process. Improvements may include mechanical, automation, or workflow.
- Works with manufacturing and capital engineering on the development of future capital projects and on the development of requirements for the project.
- Responsible for User Requirement Specification development.
- Assists cross functional teams in the execution of small-scale capital projects up to around $500,000, process improvement projects, continuous improvement projects, and equipment improvement projects.
- On larger capital projects, the engineer will be responsible for ensuring process requirements are communicated and built into the equipment/system design. The engineer will develop specifications (user, functional, and detailed design) for equipment and automation of the equipment.
- Develops and maintains overall knowledge of facility processes and products.
- Provides training on process and/or equipment modifications as required for new or existing equipment/processes.
- Acts as Subject Matter Expert for production equipment and processes for Capital Engineering, Production, Business Process Science, Quality Assurance, and Maintenance.
BASIC QUALIFICATIONS
- Bachelor of Science Degree in Engineering from an accredited school with one to three (1-3) years applicable experience in a GMP environment or Bachelor´s degree with three to five (3-5) of engineering or scientific experience outside of a GMP environment.
- In lieu of years of experience, Master´s Degree in relevant field from an accredited school with one (1) year experience in a GMP environment or at least one (1) year of engineering or two (2) years of scientific experience outside of a GMP environment.
- At least one (1) year of experience leading projects preferable.
COMPETENCIES
- Effective verbal and written communication with all levels of corporate and local management and employees.
- Ability to plan, schedule, organize, prioritize, and coordinate project activities.
- Ability to understand and work within a regulated environment.
- Experience with GAMP Automation practices and documents preferred.
- Ability to function in a leadership role as well as in a team environment.
- Ability to manage multiple projects at one time.
SKILLS
- Analytical Thinking
- Data collection and analysis
- Communication
- Customer Focus
- Data-driven Decision Making
- Planning and Organizing
- Teamwork
- Conceptual / Analytical Thinking Scope
- Delivering Results
- Leadership
DESIRED SKILLS, EXPERIENCE AND ABILITIES
STEM OPT Biotech & Pharma Job Roles in Georgia
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Search Biotech & Pharma Jobs in GeorgiaBiotech & Pharma STEM OPT Sponsorship Jobs in Georgia: Frequently Asked Questions
Which biotech and pharma companies in Georgia sponsor F-1 STEM OPT visas?
Georgia hosts a range of biotech and pharma employers with documented STEM OPT sponsorship history, including contract research organizations and biologics manufacturers concentrated around Atlanta and Peachtree City. Larger employers such as Immuno Medics, BioAtlanta member companies, and multinationals with Georgia research operations have filed Labor Condition Applications for roles. Sponsorship practices vary by employer size and role type, so verifying individual company filing history before applying is advisable.
Which cities in Georgia have the most biotech and pharma F-1 STEM OPT sponsorship jobs?
Atlanta leads Georgia in biotech and pharma STEM OPT opportunities, particularly in Midtown and Buckhead where research institutes, CROs, and biotech startups cluster near Georgia Tech and Emory University. Peachtree City and Covington host pharmaceutical manufacturing and quality operations. Augusta has a growing medical research presence tied to Augusta University Health. Most active STEM OPT sponsorship filings originate from the Greater Atlanta metro area.
What types of biotech and pharma roles typically qualify for F-1 STEM OPT sponsorship in Georgia?
Roles that fall under STEM-designated Classification of Instructional Programs codes qualify for the 24-month STEM OPT extension. In Georgia's biotech and pharma sector, qualifying positions commonly include bioinformatics analyst, quality control scientist, process development engineer, regulatory affairs associate, computational biologist, and clinical data analyst. The role must be directly related to the student's STEM degree, and the employer must be enrolled in E-Verify to participate in the STEM OPT extension program.
How do I find biotech and pharma F-1 STEM OPT sponsorship jobs in Georgia?
Migrate Mate is built specifically for international students and filters biotech and pharma jobs in Georgia by visa type, including F-1 STEM OPT, using DOL Labor Condition Application data to surface employers with verified sponsorship activity. You can search by industry, location, and authorization type to find Georgia-based employers who have historically filed for STEM OPT workers in life sciences roles, which substantially narrows your search compared to general job platforms.
Are there state-specific considerations for F-1 STEM OPT sponsorship in Georgia's biotech and pharma industry?
Georgia does not impose additional state-level visa sponsorship requirements beyond federal USCIS and DOL rules. However, Georgia's biotech sector is closely linked to the CDC's Atlanta campus and Emory University's research network, meaning some positions may involve federal contractor status, which can affect sponsorship eligibility. Employers in Georgia's pharmaceutical manufacturing corridor around Peachtree City tend to be larger and more experienced with STEM OPT compliance, including E-Verify enrollment and prevailing wage obligations under the OFLC Wage Search standards.