Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) WarehouseJob Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Excellent Benefits Package
Review our companys Total Rewards
Medical Dental & Vision benefits-effective Day 1
Paid Time Off & Holidays
401K Company Match up to 6%
Tuition Reimbursement eligible after 90 days!
Employee Referral Bonus
Employee Discount Program
Recognition Program
Charitable Gift Matching
Company Paid Parental Leave
Career Advancement Opportunities
Location/Division Specific Information
Greenville NC
RELOCATION ASSISTANCE IS NOT PROVIDED
We have industry-leading sterile injectable facilities providing solutions to take essential products from pre-clinical to the market. Pharmaceutical products come in many different dose forms including inhalations oral dose cream/ointment and injectables.
The FTZ Operations and Compliance Specialist will handle all Foreign Trade Zone activities at our Greenville facility ensuring full compliance with U.S. Customs and Border Protection (CBP) regulations international trade laws and Thermo Fishers internal policies. The role involves collaborating with government agencies internal teams and external partners to maintain seamless FTZ operations and compliance.
Key Responsibilities:
FTZ Program Development & Compliance: Develop implement and maintain FTZ programs policies SOPs and controls; ensure accurate import classification of pharmaceutical products in the Global Trade Classification (GTC) database; collaborate with shipping export and logistics teams to handle FTZ shipments in compliance with regulations.
Regulatory Compliance & Audit: Conduct periodic self-audits resolve discrepancies file timely reports to CBP and other agencies and stay current on regulatory changes affecting FTZ operations.
Cross-Functional Collaboration: Partner with management supply chain finance IT legal and other departments to ensure smooth FTZ operations; provide training and guidance on FTZ policies.
Continuous Improvement & Education: Promote a culture of trade compliance and continuous improvement; educate logistics and trade compliance teams on FTZ regulations; collaborate with government agencies for audits or informational requests.
FTZ Activation & Operational Management: Support FTZ activation and ongoing operations; ensure FTZ activities meet regulatory and corporate objectives efficiently.
Trade Law & Regulatory Monitoring: Track and communicate changes in trade laws and regulations; proactively handle regulatory risks to FTZ operations.
Required Qualifications:
Bachelors degree in International Business Logistics Supply Chain Management or related field (or equivalent experience).
35 years of FTZ operations experience with a focus on compliance (pharmaceutical experience preferred).
Strong experience developing policies procedures and controls related to FTZ management and trade compliance.
SAP experience strongly preferred; familiarity with FTZ management software (e.g. Integration Point) is a plus.
Ability to interpret and apply U.S. Customs FTZ and international trade regulations.
Excellent social skills with the ability to communicate effectively across functional areas and external partners.
Confirmed ability to develop implement and complete new programs independently.
Preferred Qualifications:
Experience in logistics supply chain management or Customs Broker license.
Knowledge of pharmaceutical regulatory standards (FDA DEA) is a plus.
Strong analytical problem-solving and organizational skills with attention to detail.
Ability to lead cross-functional teams and develop a culture of compliance.
Physical Demands & Work Environment:
Occasional lifting bending and extended standing.
Fast-paced environment with multiple priorities.
Occasional travel for audits training or meetings.
Required Experience:
IC
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