Healthcare Jobs at Vertex Pharmaceuticals with Visa Sponsorship
Vertex Pharmaceuticals hires Healthcare professionals to support clinical development, regulatory affairs, and patient access programs tied to its pipeline. The company has an established track record of sponsoring work visas for qualified candidates in this function, making it a realistic target for international job seekers.
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Get Access To All JobsJOB DESCRIPTION:
The Quality Manager is a technical resource in the principles and application of quality assurance, quality systems, and compliance. The Quality Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects, effectively ensuring alignment with corporate goals and compliance with regulatory requirements. This position reports directly to the GMP Operational Quality Senior Manager.
Key Responsibilities:
- Collaborate with internal and external business partners to resolve quality issues to ensure compliant solutions.
- Provide QA support of change controls, investigations, CAPA’s, and effectiveness checks.
- Draft, review, and manage approval of quality system documentation, including but not limited to, deviations, change controls, and CAPA’s.
- Lead meetings, as necessary, and collaborate with customer groups to ensure quality systems are monitored and established metrics are met.
- Perform Batch Record Review of Health Donar and Drug Product lots.
- Perform Lot Disposition of Critical Components and Drug Product lots.
- Perform archival activities to support lot disposition.
- Partner with External CDMOs.
- Act as subject matter expert in quality related improvement activities.
- Perform change control assessments and closure approvals.
- Collect data and report on metrics.
- Represent Vertex Quality on cross functional working teams, applying strong communication and collaboration skills.
- Participate in continuous improvement projects, identify risks and communicate gaps for process/systems to ensure the team continues to meet expanding business needs.
- Draft, review, and manage approval SOP's, Job Aids, and Work Instructions to support quality functions.
- Support regulatory agency inspections including inspection readiness activities and supporting regulatory and internal site inspections.
- Manage day-to-day activities for a Quality Assurance Associate(s)/Specialist(s), as applicable.
Minimum qualifications:
- Bachelor’s degree in Life Sciences, Engineering, Pharmacy, Chemistry, or a related discipline.
- Relevant experience in Quality Assurance, Quality Operations, or a related GMP-regulated function within biotechnology, pharmaceuticals, or advanced therapies.
- Demonstrated experience supporting GMP operations in a manufacturing or operational quality environment.
- Strong understanding of quality systems, including deviations, CAPA, change control, investigations, and document management.
- Knowledge of applicable regulatory requirements and industry expectations for GMP environments.
- Experience working cross-functionally and influencing teams in a complex operational setting.
- Strong problem-solving, communication, and organizational skills.
- Ability to manage multiple priorities and make sound quality decisions in a fast-paced environment.
Technical Skills Required:
- GMP / cGMP compliance
- Quality systems management
Pay Range:
- $70-$80/hr
Requisition Disclaimer:
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
JOB DESCRIPTION:
The Quality Manager is a technical resource in the principles and application of quality assurance, quality systems, and compliance. The Quality Manager coordinates or executes activities on a wide range of projects and takes a role in the design and execution of new projects, effectively ensuring alignment with corporate goals and compliance with regulatory requirements. This position reports directly to the GMP Operational Quality Senior Manager.
Key Responsibilities:
- Collaborate with internal and external business partners to resolve quality issues to ensure compliant solutions.
- Provide QA support of change controls, investigations, CAPA’s, and effectiveness checks.
- Draft, review, and manage approval of quality system documentation, including but not limited to, deviations, change controls, and CAPA’s.
- Lead meetings, as necessary, and collaborate with customer groups to ensure quality systems are monitored and established metrics are met.
- Perform Batch Record Review of Health Donar and Drug Product lots.
- Perform Lot Disposition of Critical Components and Drug Product lots.
- Perform archival activities to support lot disposition.
- Partner with External CDMOs.
- Act as subject matter expert in quality related improvement activities.
- Perform change control assessments and closure approvals.
- Collect data and report on metrics.
- Represent Vertex Quality on cross functional working teams, applying strong communication and collaboration skills.
- Participate in continuous improvement projects, identify risks and communicate gaps for process/systems to ensure the team continues to meet expanding business needs.
- Draft, review, and manage approval SOP's, Job Aids, and Work Instructions to support quality functions.
- Support regulatory agency inspections including inspection readiness activities and supporting regulatory and internal site inspections.
- Manage day-to-day activities for a Quality Assurance Associate(s)/Specialist(s), as applicable.
Minimum qualifications:
- Bachelor’s degree in Life Sciences, Engineering, Pharmacy, Chemistry, or a related discipline.
- Relevant experience in Quality Assurance, Quality Operations, or a related GMP-regulated function within biotechnology, pharmaceuticals, or advanced therapies.
- Demonstrated experience supporting GMP operations in a manufacturing or operational quality environment.
- Strong understanding of quality systems, including deviations, CAPA, change control, investigations, and document management.
- Knowledge of applicable regulatory requirements and industry expectations for GMP environments.
- Experience working cross-functionally and influencing teams in a complex operational setting.
- Strong problem-solving, communication, and organizational skills.
- Ability to manage multiple priorities and make sound quality decisions in a fast-paced environment.
Technical Skills Required:
- GMP / cGMP compliance
- Quality systems management
Pay Range:
- $70-$80/hr
Requisition Disclaimer:
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
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Get Access To All JobsTips for Finding Healthcare Jobs at Vertex Pharmaceuticals Jobs
Align Your Credentials to Vertex's Pipeline Focus
Vertex's Healthcare hiring centers on cystic fibrosis, sickle cell disease, and pain management programs. Tailor your CV to highlight experience in rare disease, clinical operations, or managed care, so your background maps directly to their active therapeutic areas.
Confirm Your Degree Field Supports H-1B Eligibility
Healthcare roles at biopharma companies require a directly related degree, not just any bachelor's. USCIS scrutinizes specialty occupation status for titles like Medical Science Liaison or HEOR analyst, so verify your degree field aligns with the specific role before applying.
Target Vertex Roles That Require Regulatory or Clinical Expertise
Roles in regulatory affairs, pharmacovigilance, and health economics attract sponsorship more reliably than generalist healthcare coordinator positions. Prioritizing postings that list FDA submission experience or outcomes research signals the specialized scope that justifies an H-1B petition.
Find Open Vertex Healthcare Roles on Migrate Mate
Browse Healthcare openings at Vertex Pharmaceuticals filtered by visa sponsorship on Migrate Mate. You can identify which specific roles are actively hiring and sponsoring, saving time you'd otherwise spend manually screening job boards.
Ask About LCA Filing Timing During the Offer Stage
Your employer must file a Labor Condition Application with the DOL before USCIS can receive the H-1B petition. During offer negotiations, ask Vertex's immigration team for their typical LCA-to-petition timeline so your start date aligns with the processing window.
Prepare for Green Card Sponsorship Conversations Early
Vertex has sponsored EB-2 and EB-3 petitions for Healthcare professionals. If long-term U.S. residency is your goal, ask during final-round interviews whether the role has a defined PERM pathway, since the labor certification process can take 18 months or more to complete.
Healthcare at Vertex Pharmaceuticals jobs are hiring across the US. Find yours.
Find Healthcare at Vertex Pharmaceuticals JobsFrequently Asked Questions
Does Vertex Pharmaceuticals sponsor H-1B visas for Healthcares?
Yes, Vertex Pharmaceuticals sponsors H-1B visas for Healthcare professionals in qualifying specialty occupation roles. Positions in regulatory affairs, medical affairs, health economics, and clinical operations are among those that have historically supported sponsorship. The role must require a bachelor's degree or higher in a directly related field to meet USCIS specialty occupation standards.
Which visa types are commonly used for Healthcare roles at Vertex Pharmaceuticals?
H-1B is the primary nonimmigrant visa for Healthcare professionals at Vertex, covering roles that require specialized scientific or clinical expertise. For candidates pursuing permanent residence, Vertex has supported Green Card sponsorship through EB-2 and EB-3 employment-based categories, typically using the PERM labor certification process for positions that do not qualify for a national interest waiver.
What qualifications does Vertex Pharmaceuticals expect for Healthcare roles?
Vertex typically requires a bachelor's degree or higher in a field directly relevant to the role, such as pharmacy, life sciences, public health, or health economics. Advanced degrees like a PharmD, MPH, or PhD are common for senior positions. Experience in biopharma, rare disease, FDA regulatory processes, or outcomes research strengthens applications for most Healthcare openings.
How do I apply for Healthcare jobs at Vertex Pharmaceuticals?
Applications are submitted through Vertex's careers portal. Search by department or therapeutic area to surface Healthcare-specific openings. If you need visa sponsorship, filter for roles where sponsorship is explicitly offered. You can also browse verified Healthcare positions at Vertex on Migrate Mate, which surfaces roles actively open to sponsored candidates and saves time screening postings manually.
How do I plan my timeline if I need H-1B sponsorship for a Vertex Healthcare role?
If you are not currently in H-1B status, the cap-subject lottery in April is the main entry point, with employment starting October 1 at the earliest. Vertex would need to register you in March. If you hold OPT or STEM OPT, you may be able to start sooner while the petition is pending. Build this calendar into your job search so offers and timelines align.
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