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Tech Transfer Lead Jobs (NOW HIRING)

Lead a portfolio of approximately 10 concurrent mAb drug substance technology transfer programs, managing timelines, milestones, deliverables, risks, and cross-functional dependencies. * Drive ...

Lead a portfolio of approximately 10 concurrent mAb drug substance technology transfer programs, managing timelines, milestones, deliverables, risks, and cross-functional dependencies. * Drive ...

Lead technology transfer projects from bench, pilot, or external development organizations into the iPROOF facility. Develop and maintain technology transfer packages including; process descriptions ...

NY · On-site

$150 - $230/hr

Lead the end-to-end technology transfer process from internal development sites, client sites, or third-party facilities into the Middletown site. * Experience with Oral Solid Dosage (OSD) is a must ...

Showing results 41-60

Tech Transfer Lead information

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$31K

$52.6K

$77.5K

How much do tech transfer lead jobs pay per year?

As of Aug 12, 2026, the average yearly pay for tech transfer lead in the United States is $52,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $57,000.00 per year, depending on experience, location, and employer.

What is the difference between Tech Transfer Lead vs Tech Transfer Specialist?

AspectTech Transfer LeadTech Transfer Specialist
Required CredentialsBachelor's or Master's in science/engineering, experience in tech transferSimilar educational background, often with less experience required
Work EnvironmentLeads projects, coordinates teams, manages tech transfer processesSupports tech transfer activities, executes tasks under supervision
Employer & Industry UsagePharmaceutical, biotech, or research institutionsSame industries, often within R&D or licensing departments

The main difference between a Tech Transfer Lead and a Tech Transfer Specialist lies in their responsibilities and experience level. The Lead manages projects and teams, while the Specialist supports and executes specific tasks. Both roles require similar educational backgrounds and are common in biotech and pharma industries.

What is a tech transfer lead?

Tech Transfer Leads are professionals responsible for managing the process of transferring technology, knowledge, or innovations from research institutions or companies to external partners or the commercial market. Their role involves evaluating new technologies, negotiating licensing agreements, ensuring compliance with legal and regulatory requirements, and facilitating collaboration between inventors and industry. They play a critical role in bridging the gap between research and practical application, helping to bring scientific discoveries to market and drive economic growth.

What are the key skills and qualifications needed to thrive as a tech transfer lead, and why are they important?

To thrive as a Tech Transfer Lead, you need expertise in technology transfer processes, project management, and a strong background in science or engineering, often supported by advanced degrees. Familiarity with intellectual property management systems, regulatory compliance tools, and technology licensing platforms is typical, along with certifications such as CLP (Certified Licensing Professional) being advantageous. Excellent communication, negotiation, and stakeholder management skills distinguish top performers in this position. These competencies are crucial for ensuring seamless transfer of technologies from development to commercialization, maximizing value for both organizations and partners.

What are the main challenges a tech transfer lead faces during the handover of new technologies from R&D to manufacturing?

A Tech Transfer Lead often navigates challenges such as ensuring clear communication between R&D and manufacturing teams, aligning documentation and process standards, and troubleshooting unforeseen technical issues during scale-up. It’s common to encounter discrepancies between lab-scale processes and full-scale production, requiring careful adjustment and problem-solving. The role also involves coordinating cross-functional teams and managing tight project timelines while maintaining quality and compliance standards.
Infographic showing various Tech Transfer Lead job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 9% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $52,560 per year, or $25.3 per hour.

Associate Director, Technical Operations - Small Molecule Drug Product

Merck & Co.

Elkton, VA • On-site

$180 - $240/hr

Other

Posted 26 days ago


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Overview

We have an exciting opportunity for an Associate Director, Technical Operations - Small Molecule Drug Product at our Elkton Site in Virginia, USA. At our company, we aim to be a premier research-intensive biopharmaceutical company, using leading-edge science to advance health worldwide. This site is designed to move quickly and reliably, receiving technology transfers from commercialization sites and moving into production with a focus on quality, safety, and operational excellence.

You will be part of a team committed to a safe, environmentally responsible, and compliant workplace where people can do their best work. We are building small molecule expertise in the U.S. and seek team members who want to grow their skills, improve operations, and contribute to a site positioned for future growth. The successful candidate will provide technical leadership and operational support for the startup, technology transfer, validation, and ongoing commercial manufacture of oral solid dosage forms.

This role is responsible for leading technical activities across assigned processes and projects, supporting the capital project and facility startup phase through to commercialization and lifecycle management. The Associate Director will ensure safe, compliant, and reliable process performance while driving continuous improvement and technical excellence.

Key Responsibilities
  • Technical Leadership
    • Recognized subject matter expert in Drug Product process support, and commercial manufacturing
    • Provide technical oversight and hands-on leadership for oral solid dose manufacturing processes, including:
      • Blending and granulation (where applicable)
      • Roller compaction (dry granulation)
      • Tablet compression
      • Film coating and finishing operations
    • Support the Capital Project Team, contributing to design, commissioning, qualification, and startup readiness
    • Lead process scale-up, technology transfer, and validation (pre-PPQ, PPQ) activities for assigned processes
    • Drive improvements in process performance, yield, robustness, and impurity control
    • Analyse technical data and support decision-making for process performance and improvements
    • Identify and escalate risks, proposing practical, science-based solutions
  • Technology Transfer
    • Lead and execute technology transfer activities for assigned processes across internal sites and external partners
    • Support development and execution of tech transfer plans aligned with project timelines
    • Provide technical support for:
      • Process fit assessments
      • Scale-up strategy from development to commercial scale
      • Equipment capability and process comparability assessments
    • Ensure accurate process documentation, knowledge transfer, and batch record readiness
    • Support process validation and continued process verification
  • Operational Excellence
    • Partner with Manufacturing to ensure safe, efficient, and reliable plant performance
    • Provide direct technical support to:
      • Campaign preparation, execution, and follow-up
      • Process troubleshooting during manufacturing
    • Lead and support deviation investigations, OOS, and CAPA, applying structured root cause analysis
    • Monitor process performance and cycle times, identifying improvement opportunities
    • Drive continuous improvement initiatives for yield, cycle time, and cost
    • Support process optimisation and debottlenecking activities
  • Regulatory & Compliance
    • Ensure assigned processes operate in compliance with cGMP and regulatory expectations
    • Support inspection readiness and audit activities
    • Contribute to regulatory submissions and responses, including data generation and technical input
    • Ensure data integrity and adherence to quality and safety standards
    • Maintain compliance from startup through commercial operations
  • Cross-functional Leadership
    • Collaborate with Engineering, Capital Projects, R&D, Quality, Supply Chain, and Manufacturing
    • Act as a technical representative for assigned processes within cross-functional teams
    • Support technology transfer and process improvements across the network
    • Participate in interactions with external partners and CMOs as required
    • Contribute to technical reviews and governance forums
  • People, Capability & Business Leadership
    • Lead and develop a team of technical specialists and engineers
    • Provide coaching, technical guidance, and performance feedback
    • Support resource planning and execution of departmental priorities
    • Contribute to budget tracking and departmental administration
    • Support recruitment, onboarding, and capability development initiatives
Qualifications
  • Degree (BSc/BEng/Masters) or higher in Chemical Engineering, Pharmaceutics, Pharmaceutical Sciences, or related discipline
  • Significant experience (typically 10+ years) in:
    • Oral solid dose manufacturing, formulation, or process development
  • Strong background in:
    • Process engineering and scale-up
    • Process, equipment, and cleaning validation
  • Working knowledge of:
    • cGMP manufacturing operations
    • Regulatory expectations and inspection readiness
  • Experience with:
    • Deviation management and investigations
    • Electronic batch records and process systems (e.g., DeltaV)
  • Exposure to capital projects, CQV, and facility startup
  • Strong analytical, problem-solving, and communication skills
  • Ability to work effectively across cross-functional teams and multiple priorities
Our Culture

We keep the patient at the heart of everything we do and strive to deliver solutions for some of the world\'s most challenging healthcare needs. We believe breakthrough innovation happens when experienced leaders empower talented teams in an inclusive environment.

If you are ready to:

  • Support delivery of new Drug Product manufacturing capability
  • Drive operational and technical excellence in Oral Solid Dose production
  • Develop your leadership capability in a high-impact environment

We encourage you to apply.

Additional Information
  • Requisition ID: R407466
  • Job Posting End Date: 08/15/2026
  • Travel Requirements: 10%
  • Relocation: Domestic
  • VISA Sponsorship: No

Equal Employment Opportunity Employer; we provide equal opportunities to all employees and applicants and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other legally protected characteristics. We comply with applicable affirmative action requirements for protected veterans and individuals with disabilities.

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