Remote Jobs at Teva Pharmaceuticals

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

HealthcarePharmaceuticalsBiotechnology

At Teva, we're proud to be a different kind of global pharmaceutical leader, one that operates across the full spectrum of innovation to reliably deliver medicines to patients worldwide. For over 120 years, our commitment to bettering health has never wavered. Every day, we challenge ourselves to push the boundaries of science, discover life-changing treatments, and deliver quality medicines. If patients have a need, we’re already working to address it. Because here, we are all in for better health. Learn more at www.tevapharm.com. Please note that adverse effects for any of our products should be reported to: [email protected] Product-specific questions should be directed to Teva or Teva Group subsidiaries in your country. Contact details and Teva's Pharmacovigilance Privacy Policy may be found here: http://www.tevapharm.com/contact_us/

Teva Pharmaceuticals logo
7d

Manager, Medical Writing

Teva Pharmaceuticals

Lead and oversee clinical regulatory writing at Teva Pharmaceuticals for drug development and product registration. Write study reports, protocols, IBs, Module 2.5/2.7 documents.

🇺🇸 United States
Full-time
$112,080 - $140,100 per year
Mid Level
Senior
✏️ Content Writer
Vault
Teva Pharmaceuticals logo
37d

Senior Director, IT Operations

Teva Pharmaceuticals

Senior Director leading IT strategy execution PMO and portfolio at Teva Pharmaceuticals, managing global IT teams and compliance.

🇺🇸 United States
Full-time
$236,000 - $309,000 per year
Senior
⚙️ Operations
PMP
Teva Pharmaceuticals logo
54d

Senior Manager, Medical Writing

Teva Pharmaceuticals

Oversees clinical regulatory documents for drug development at Teva Pharmaceuticals. Guides medical writing teams and ensures regulatory compliance.

Teva Pharmaceuticals logo
54d

Director, Therapy Area Head, Medical Writing

Teva Pharmaceuticals

Teva seeks a Director of Global Regulatory Medical Writing to lead regulatory docs. Oversees writing, templates, metrics, and team development for drug registrations.