
Sr Technical Lead Project Manager HTC Global Services Inc
- Full-time
- Employee
| Location | East Hanover, NJ |
| Industry | Biotechnology/Pharmaceuticals |
| Salary | $126,000–$234,000 Per Year |
| Company Size | 10,000 employees or more |
| Year Founded | 1996 |
Job ID
REQ-10081687
Jul 01, 2026
USA
Available in: English
Summary
Location: Morrisville, NCStep into a pivotal role where your expertise drives the successful launch of life-changing medicines. As a Technical Transfer Lead, you will own and lead complex technology transfer initiatives, shaping how innovative therapies move from development to commercial manufacturing. Working at the heart of a highly collaborative environment, you will partner with cross-functional teams to deliver robust, compliant, and efficient processes-ensuring patients receive high-quality treatments, on time and at scale.
About the Role
Key ResponsibilitiesLead end-to-end technical transfer projects, ensuring timelines, scope, and quality objectives are achievedAct as site point of contact for transfer activities, aligning stakeholders across Technical Development, Supply Chain, Manufacturing, Quality, HSE, and other sitesDevelop and execute transfer and validation strategies, including process, cleaning, packaging and supportive studies. Coordinate technical, regulatory, and validation batches, ensuring documentation readiness and complianceEstablish and lead cross-functional project teams, driving execution, risk mitigation, and decision-makingEnsure compliance with cGMP and readiness for inspections and pre-approval auditsDrive process improvements and optimization to support successful product launches and ongoing manufacturing excellenceEssential RequirementsBachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or equivalent scientific degreeMinimum 5 years of experience in oral solid dosage pharmaceutical manufacturingDemonstrated experience in technical transfer, process scale-up, and validation activitiesStrong knowledge of current Good Manufacturing Practices and regulatory requirementsProven project management skills with ability to lead cross-functional teamsStrong technical expertise in pharmaceutical processes, with ability to solve complex manufacturing challengesDesirable RequirementsMaster of Science or equivalent experienceThe salary for this position is expected to range between $126,000 - $234,000 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.#LI-Onsite
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureBenefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally.Read our handbook (PDF 30 MB)
EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.Accessibility & Reasonable AccommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Division
Operations
Business Unit
Production / Manufacturing
Location
USA
State
North Carolina
Site
Durham
Company / Legal Entity
U473 (FCRS = US473) Novartis Gene Therapies
Functional Area
Technical Operations
Job Type
Full time
Employment Type
Regular
Shift Work
No
Technical Operations Operations USA
Job ID
REQ-10081687
Technical Transfer Lead
Apply to Job
Job ID
REQ-10081687
Technical Transfer Lead
Apply to Job
Novartis provides healthcare solutions that improve and extend people’s lives. We use science-based innovation to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. Our company is focused on industry-leading divisions with innovation power and global scale: pharmaceuticals, eye care and generic medicines Novartis is headquartered in Basel, Switzerland. Novartis Group companies employ approximately 120,000 associates and its products are available in more than 180 countries around the world.


