Biotech & Pharma TN Sponsorship Jobs in Connecticut
Connecticut's biotech and pharma sector is anchored by major employers like Pfizer, Cigna, and Alexion (AstraZeneca) alongside a growing cluster of life sciences firms in New Haven, Hartford, and Groton. Canadian and Mexican professionals in scientific, engineering, and clinical roles can pursue TN visa sponsorship with Connecticut employers actively hiring in drug development, regulatory affairs, and research.
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About CooperSurgical
JOB DESCRIPTION
CooperSurgical is a leading fertility and women’s healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division of CooperCompanies, we're driven by a unified purpose to enable patients to experience life's beautiful moments. Guided by our shared values – dedicated, innovative, friendly, partners, and do the right thing – our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women’s and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions.
Work location: Trumbull, CT or Livingston, NJ (on-site)
Scope:
The Supplier Quality Engineer Lead is responsible for strategic leadership and execution of the Global Supplier Quality Management Program. This role provides functional leadership across supplier quality activities, ensures regulatory and QMS compliance, and drives continuous improvement across critical and strategic suppliers. The Lead operates with a high degree of autonomy, influences cross‑functional and senior leadership decisions, and sets direction for supplier quality governance, risk management, and performance improvement.
Job Summary:
The Supplier Quality Engineer Lead governs supplier qualification, compliance, auditing, development, and escalation activities for high‑risk, high‑impact, and strategic suppliers. This role owns supplier quality strategy, serves as escalation point for complex supplier issues and regulatory interactions, and plays a key role in management review, audit readiness, and organizational quality maturity. The position provides leadership and mentoring to Supplier Quality Engineers and partners closely with Procurement, Operations, Engineering, Regulatory, and Business Leaders.
Responsibilities
Supplier Quality Leadership & Strategy
- Define and lead supplier quality strategy aligned with business objectives and regulatory requirements.
- Provide functional leadership and mentoring to Supplier Quality Engineers.
- Serve as escalation point for supplier quality issues, Risk 1 suppliers, outsourced processes, and supply chain disruptions.
- Influence senior leadership decisions related to supplier risk, sourcing strategy, and business continuity.
Supplier Audits & Regulatory Compliance
- Lead planning and execution of global supplier audit programs (onsite, remote, desktop).
- Ensure effective management, escalation, and closure of audit findings and compliance gaps.
- Act as primary Quality representative for supplier-related regulatory inspections, notified body audits, and health authority inquiries.
Supplier Performance & Risk Governance
- Establish and oversee supplier risk classification, risk assessment, and mitigation frameworks.
- Review, trend, and present supplier performance metrics and risk data to Management Review and senior leadership.
- Ensure proactive identification of systemic supplier risks and continuous monitoring of supplier health.
Corrective Action, Escalation & Change Management
- Provide oversight and escalation leadership for Supplier Corrective Action Requests (SCARs), ensuring robust root cause and sustained effectiveness.
- Lead supplier-related Nonconforming Material Reports (NCMRs) and support critical escalations.
- Evaluate and manage Supplier Change Notifications (SCNs) and change impact assessments.
Supplier Development & Continuous Improvement
- Lead supplier development initiatives focused on quality improvement, compliance, delivery performance, and resiliency.
- Support New Product Introduction (NPI), supplier transfers, localization, and dual-sourcing initiatives.
- Provide quality leadership for supplier-facing validation activities (IQ/OQ/PQ, PPAP, qualifications).
Quality Systems & Governance
- Develop, Maintain governance and continuous improvement of Supplier Quality Agreements, SOPs, workflows, and metrics.
- Ensure supplier documentation, records, and controls remain compliant with QMS and regulatory expectations.
- Drive cross-functional alignment across the supplier lifecycle from selection through post-market support.
Travel:
This position may require 15-30% domestic and/or international travel.
Qualifications
Knowledge, Skills and Abilities:
- Expert knowledge of FDA QSR (21 CFR 820), ISO 13485, EU MDR, ISO 14971.
- Strong leadership experience in supplier quality governance, audits, CAPA/SCAR, and risk management.
- Demonstrated ability to lead through influence and manage complex cross-functional initiatives.
- Advanced problem-solving and quality tool expertise (RCA, FMEA, statistical analysis).
- Executive-level communication skills with internal leadership and external suppliers.
- Proficiency with MS Office, Minitab, ERP systems, and eQMS platforms.
Experience:
- 7+ years experience in Supplier/Vendor Quality Management.
- 10+ years experience in a regulated quality environment (medical device, pharma, life sciences).
- Proven leadership of high-risk suppliers, regulatory interactions, and global supplier initiatives.
Work Environment:
- Manufacturing, clean room, warehouse, and office environments.
- May require extended periods of sitting, standing, and movement in production and supplier facilities.
Education:
- Bachelor’s Degree in Chemical, Electro-Mechanical, Industrial, Biomedical, Bioprocess Engineering or related to Life Science field or equivalent experience or skillset.
- CQE, ASQ, APICS, Six Sigma Green Belt/Black Belt preferred.
Our Benefits:
As an employee of CooperSurgical, you'll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits.
To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.
For U.S. locations that require disclosure of compensation, the starting base pay for this role is between $120,000.00 - $150,000.00 annually. The actual base pay includes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.
TN Biotech & Pharma Job Roles in Connecticut
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Search Biotech & Pharma Jobs in ConnecticutBiotech & Pharma TN Sponsorship Jobs in Connecticut: Frequently Asked Questions
Which biotech and pharma companies sponsor TN visas in Connecticut?
Connecticut's largest life sciences employers include Pfizer's Groton research campus, Alexion Pharmaceuticals (now part of AstraZeneca) in New Haven, and Boehringer Ingelheim in Ridgefield. Smaller contract research organizations and specialty biotech firms in the New Haven and Hartford areas have also filed TN visa sponsorships for scientific and technical roles. Sponsorship patterns vary by company size, hiring volume, and the specific role's TN eligibility.
Which cities in Connecticut have the most biotech and pharma TN sponsorship jobs?
New Haven is Connecticut's most active life sciences hub, driven by Yale University's research ecosystem and nearby biotech spinouts. Groton is a major destination given Pfizer's large R&D campus there. Hartford and Ridgefield also have notable pharma presence. For roles spanning manufacturing and clinical operations, the I-95 and Route 1 corridor connecting these cities concentrates a significant share of available positions.
What types of biotech and pharma roles typically qualify for TN sponsorship?
TN visa eligibility in biotech and pharma most commonly covers roles that align with designated USMCA professional categories, including Biochemist, Chemist, Pharmacist, Pharmacologist, Scientific Technician, and Computer Systems Analyst for informatics positions. Regulatory affairs specialists and clinical research associates may qualify depending on how the role is defined and whether the applicant holds the requisite degree in a directly related field. Each classification has specific educational and professional requirements under USMCA.
How do I find biotech & pharma TN sponsorship jobs in Connecticut?
Migrate Mate is built specifically for professionals seeking U.S. jobs that include visa sponsorship, including TN sponsorship in biotech and pharma. You can filter by Connecticut, by industry, and by TN visa type to see live postings from employers actively open to sponsoring the visa. This is more targeted than broad job searches because listings are curated for international candidates who need sponsorship confirmed upfront.
Are there any Connecticut-specific considerations for TN sponsorship in biotech and pharma?
Connecticut's life sciences cluster is closely tied to academic medical centers and federal research funding, which can influence hiring timelines and the types of roles available. Some positions at university-affiliated research institutions may involve additional compliance steps. Connecticut has no state-level visa restriction, but employers in regulated pharmaceutical manufacturing must ensure TN job duties align precisely with the USMCA category claimed, as discrepancies are a common source of TN complications.