Biotech & Pharma H-1B1 Singapore Sponsorship Jobs in Alabama
Alabama's biotech and pharma sector spans Huntsville's growing life sciences corridor, Birmingham's UAB-anchored research ecosystem, and contract manufacturing operations statewide. Singaporean professionals on the H-1B1 visa can find sponsoring employers in research, clinical development, and manufacturing roles, with companies like Bioventus, PPD, and regional CROs actively hiring specialty occupation talent.
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Get Access To All JobsAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Lilly is currently constructing an advanced manufacturing facility for the production of API molecules. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the leadership team for the startup of a manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.
Main Purpose and Objectives of Position:
The Senior Director HSE is responsible for developing, implementing, and maintaining HSE programs and systems at the Lilly manufacturing site. This includes oversight of all site operations—manufacturing, labs, utilities, waste, emergency response, and administrative areas—ensuring compliance with global and regulatory standards.
This role leads the site HSE team, supports employee development, and serves as the primary liaison with corporate HSE to ensure alignment and readiness for regulatory inspections.
As a member of the Lilly Site Lead Team, the Senior Director contributes to strategic planning and cross-functional leadership. During the project delivery and startup phase (2029–2030), the role will focus on building HSE systems, processes, and culture to support GMP operations and enable a safe, compliant launch of full-scale manufacturing.
Key Responsibilities for this role include:
Pre-Startup and Startup Phase:
- Lead collaboratively and inclusively across all aspects of operational readiness and startup.
- Build an HSE organization with the capability, capacity, and culture to support safe, compliant, and efficient operations.
- Define HSE priorities and roadmap; implement systems and processes using internal expertise and external best practices.
- Establish and lead the site HSE Lead Team, embedding safety and environmental focus throughout project delivery and startup.
- Serve as a key HSE stakeholder during project execution—guiding design, startup planning, and contractor safety in partnership with Global Facilities Delivery.
- Develop and scale the HSE organization to support full GMP manufacturing, including environmental and PSM capabilities.
- Build strong technical partnerships with corporate/global teams and lead site-level execution of strategic initiatives.
Post Startup:
- Own the HSE Management System to ensure compliance with regulations and Lilly Global standards.
- Define and manage HSE priorities, roadmap, business initiatives, metrics, and the HSE Plan in collaboration with functional partners.
- Ensure ongoing compliance with reporting and recordkeeping requirements, including Title V.
- Benchmark best practices across the Lilly network and external industry.
- Develop future HSE leadership for both site and global roles.
- Escalate critical HSE issues to site and corporate leadership as needed.
Requirements
- Bachelor’s Degree in relevant discipline
- 5+ years of experience leading HSE teams and programs (preferably with PSM and API manufacturing experience)
Additional Preferences:
- Proven leadership of HSE programs and management systems in manufacturing, including Process Safety Management (PSM).
- Experience implementing and managing environmental compliance programs, including Title V reporting and recordkeeping.
- Skilled in engaging with regulatory agencies on environmental, health, and safety matters.
- Strong ability to build effective relationships across all levels, including close collaboration with the Site Leadership Team.
- Demonstrated success in developing high-performing, engaged teams and fostering a strong safety culture.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$163,500 - $239,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Lilly is currently constructing an advanced manufacturing facility for the production of API molecules. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the leadership team for the startup of a manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.
Main Purpose and Objectives of Position:
The Senior Director HSE is responsible for developing, implementing, and maintaining HSE programs and systems at the Lilly manufacturing site. This includes oversight of all site operations—manufacturing, labs, utilities, waste, emergency response, and administrative areas—ensuring compliance with global and regulatory standards.
This role leads the site HSE team, supports employee development, and serves as the primary liaison with corporate HSE to ensure alignment and readiness for regulatory inspections.
As a member of the Lilly Site Lead Team, the Senior Director contributes to strategic planning and cross-functional leadership. During the project delivery and startup phase (2029–2030), the role will focus on building HSE systems, processes, and culture to support GMP operations and enable a safe, compliant launch of full-scale manufacturing.
Key Responsibilities for this role include:
Pre-Startup and Startup Phase:
- Lead collaboratively and inclusively across all aspects of operational readiness and startup.
- Build an HSE organization with the capability, capacity, and culture to support safe, compliant, and efficient operations.
- Define HSE priorities and roadmap; implement systems and processes using internal expertise and external best practices.
- Establish and lead the site HSE Lead Team, embedding safety and environmental focus throughout project delivery and startup.
- Serve as a key HSE stakeholder during project execution—guiding design, startup planning, and contractor safety in partnership with Global Facilities Delivery.
- Develop and scale the HSE organization to support full GMP manufacturing, including environmental and PSM capabilities.
- Build strong technical partnerships with corporate/global teams and lead site-level execution of strategic initiatives.
Post Startup:
- Own the HSE Management System to ensure compliance with regulations and Lilly Global standards.
- Define and manage HSE priorities, roadmap, business initiatives, metrics, and the HSE Plan in collaboration with functional partners.
- Ensure ongoing compliance with reporting and recordkeeping requirements, including Title V.
- Benchmark best practices across the Lilly network and external industry.
- Develop future HSE leadership for both site and global roles.
- Escalate critical HSE issues to site and corporate leadership as needed.
Requirements
- Bachelor’s Degree in relevant discipline
- 5+ years of experience leading HSE teams and programs (preferably with PSM and API manufacturing experience)
Additional Preferences:
- Proven leadership of HSE programs and management systems in manufacturing, including Process Safety Management (PSM).
- Experience implementing and managing environmental compliance programs, including Title V reporting and recordkeeping.
- Skilled in engaging with regulatory agencies on environmental, health, and safety matters.
- Strong ability to build effective relationships across all levels, including close collaboration with the Site Leadership Team.
- Demonstrated success in developing high-performing, engaged teams and fostering a strong safety culture.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$163,500 - $239,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
Biotech & Pharma Job Roles in Alabama
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Search Biotech & Pharma Jobs in AlabamaBiotech & Pharma Jobs in Alabama: Frequently Asked Questions
Which biotech and pharma companies sponsor H-1B1 Singapore visas in Alabama?
Alabama employers with documented H-1B1 visa and related specialty occupation sponsorship activity include contract research organizations operating near Birmingham, pharmaceutical manufacturers in the Huntsville corridor, and UAB-affiliated biotech spinouts. Larger national employers such as Thermo Fisher Scientific and Charles River Laboratories maintain Alabama operations and have filed Labor Condition Applications for specialty roles. Sponsorship history varies by site and role, so checking DOL disclosure data through the OFLC Wage Search is the most reliable verification method.
Which cities in Alabama have the most biotech and pharma H-1B1 Singapore sponsorship jobs?
Birmingham concentrates the most biotech and pharma activity, driven by the University of Alabama at Birmingham medical research complex and affiliated industry partners. Huntsville has expanded its life sciences presence alongside its aerospace and defense base, attracting CROs and specialty manufacturers. Mobile hosts pharmaceutical distribution and manufacturing operations. Most H-1B1-eligible specialty occupation postings in Alabama originate from these three metro areas, with Birmingham holding the largest share of research-oriented roles.
What types of biotech and pharma roles typically qualify for H-1B1 Singapore sponsorship?
Roles that require at least a bachelor's degree in a directly related field qualify as specialty occupations under H-1B1 rules. In Alabama's biotech and pharma sector, qualifying positions commonly include research scientists, clinical research associates, biostatisticians, regulatory affairs specialists, quality assurance engineers, and bioinformatics analysts. O*NET occupation profiles identify the standard educational requirements for each job title, which employers use when preparing the Labor Condition Application to support an H-1B1 petition.
How do I find biotech and pharma H-1B1 Singapore sponsorship jobs in Alabama?
Migrate Mate filters job listings specifically for H-1B1 Singapore-eligible roles in Alabama's biotech and pharma sector, surfacing employers with verified DOL Labor Condition Application filing history for relevant occupation codes. This lets Singaporean professionals focus on companies that have already demonstrated willingness to sponsor, rather than manually screening general postings. Search by city or role type on Migrate Mate to narrow results to Birmingham, Huntsville, or specific functions like clinical research or quality assurance.
Are there state-specific or industry-specific considerations for H-1B1 Singapore sponsorship in Alabama?
Alabama does not impose additional state-level visa sponsorship requirements beyond federal H-1B1 rules, so the standard DOL Labor Condition Application and USCIS petition process applies. Industry-specific considerations include the prevalence of government-contracted research in Huntsville, which can affect employer eligibility for certain visa categories. Pharmaceutical manufacturing roles may also require specific occupational licensing under Alabama Board of Pharmacy rules, which operates independently of the H-1B1 immigration process and should be confirmed with the relevant licensing board.
What is the prevailing wage for H-1B1 Singapore biotech & pharma jobs in Alabama?
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.