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Pharmaceutical Technology Transfer Jobs (NOW HIRING)

Phlow Corp.

Sr. Director, Tech Transfer

Richmond, VA · On-site

As the Sr. Director of Tech Transfer, you will play a pivotal role in ensuring the seamless transition of pharmaceutical products and processes from R&D to manufacturing or between manufacturing ...

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How much do pharmaceutical technology transfer jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for pharmaceutical technology transfer in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What are some common challenges faced during pharmaceutical technology transfer and how are they typically addressed?

One of the main challenges in pharmaceutical technology transfer is ensuring that product quality and process consistency are maintained when moving from development to manufacturing, or between different sites. Variations in equipment, scale, and site-specific practices can introduce risks, so clear documentation, risk assessments, and rigorous validation protocols are essential. Close cross-functional collaboration among R&D, quality assurance, manufacturing, and regulatory teams helps to identify and resolve potential issues early. Effective communication, thorough training, and detailed project planning are crucial for a successful transfer.

What is pharmaceutical technology transfer?

Pharmaceutical technology transfer is the process of transferring the knowledge, processes, and technologies necessary to manufacture pharmaceutical products from one facility, organization, or country to another. This process ensures that the quality, efficacy, and safety of the product are maintained throughout the transition. It typically involves documentation, training, equipment qualification, and process validation to meet regulatory requirements. Technology transfer is essential for scaling up production, introducing new products, or shifting manufacturing sites.

What are the key skills and qualifications needed to thrive in Pharmaceutical Technology Transfer, and why are they important?

To excel in Pharmaceutical Technology Transfer, a solid background in pharmaceutical sciences, process engineering, or chemistry—often with a relevant degree—is essential. Familiarity with validation protocols, cGMP regulations, and tools like process mapping software, as well as experience with documentation systems, is typically required. Strong project management, cross-functional communication, and problem-solving skills help professionals effectively coordinate between R&D, manufacturing, and quality teams. These competencies ensure smooth, compliant, and efficient transfer of processes and products from development to commercial manufacturing.
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Pharmaceutical Technology Transfer jobs near you
Infographic showing various Pharmaceutical Technology Transfer job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 5% Part Time, and 3% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.
Senior Manager, Pharmaceutical Sciences

Senior Manager, Pharmaceutical Sciences

Shionogi Inc.

Florham Park, NJ • On-site

$135K - $165K/yr

Other

Posted 26 days ago

Job description

Overview
The Senior Manager, Pharmaceutical Sciences applies broad pharmaceutical sciences and CMC expertise to develop and maintain commercial products that are safe, effective, compliant, and robust across the product lifecycle. This role will provide technical leadership for an oral suspension product and a sterile injectable product, including formulation/process development, technology transfer, external manufacturing (CDMO/CMO) oversight, investigations, and post-approval lifecycle management.
Responsibilities
  • Interact with external manufacturing partners and testing laboratories in support of management of development and tech transfer projects - clinical supplies, commercial and post-marketed products.
  • Participate in the development and review of validation strategies for new products and processes, including assessment of vendor change controls, risk assessments, annual product reports, and process validation protocols and reports.
  • Provide technical support for Supply Chain, Quality Assurance (QA) and Regulatory Affairs Departments, and Provide scientific direction and expertise to cross-functional teams.
  • Be responsible for Risk Management activities including risk assessment, impact analysis and Failure Modes and Effects Analysis (FMEA). Maintain working knowledge of available pharmaceutical technology in the marketplace and evaluate suitability for use with current or future development projects; as well as marketed products
  • Act as the Technical Lead and project manager on multidisciplinary development teams, maintaining responsibility and authority to make technical recommendations and managerial decisions that directly impact the project timeline and budget.
  • Participate in the selection of technology vendors and development partners.
  • Provide project updates (monthly reports, data summaries) to management.
  • Serve as the primary technical liaison to development laboratories and CMOs for key projects, and collaborate with Shionogi Japan colleagues on technology transfer activities while overseeing drug development and manufacturing processes.
  • Optimize design for manufacturing from cost reduction to line expansion capabilities.
  • Review IQ/OQ/PQ activities that are related to manufacturing processes.
  • Partner with manufacturing partners to identify process improvement needs and support the design and implementation of enhanced processes and practices.
  • Participate in due diligence CMC reviews for new business opportunities.
  • Participate in lab work in design and development of novel pharmaceutical dosage forms.
Minimum Job Requirements
  • Master's Degree in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Polymer Science, or related discipline required; PhD preferred
  • 8+ years of progressive pharmaceutical development experience (or equivalent), including formulation and process development through tech transfer and commercial support.
  • Demonstrated experience supporting oral liquid/suspension product and/or sterile injectable (aseptic processing/fill-finish and/or sterile filtration/terminal sterilization strategy)
  • Functions independently with minimal guidance while managing multiple, varied project responsibilities.
  • Must offer experience in pharmaceutical analysis, formulation development, and manufacturing scale up/technology transfer
  • Experience developing Validation Strategies for new products and processes.
  • Thorough knowledge of current GMPs (Good Manufacturing Practices)
  • Demonstrates expertise in ICH guidelines and regulatory authority requirements to ensure compliant pharmaceutical development, testing, documentation, and submissions
  • Thorough knowledge of functions and disciplines that contribute to the development, manufacturing, regulation and distribution of products intended for the pharmaceutical marketplace
  • Strong oral and written communication, including the ability to communicate to colleagues, business partners, stakeholders, and upper management
  • Ability to influence and coach positive behaviors within a matrixed organization as well as with the CMOs
  • Strong presentation skills
  • Strong analytical, critical reasoning, and problem-solving skills
  • Must be innovative, resourceful, proactive, and consistently effective
  • Adept at the use of word processors, spreadsheets, and other common software
  • Must be able to travel up to 40% - domestic and international
  • Experience managing others in a matrix type environment is a plus

Other Requirements
  • Must live a commutable distance to our US Corporate Headquarters in Florham Park, NJ. Office presence required 50% per month, at least 2-3 days per week.

Additional Information
The base salary range for this full-time position is $135,000 - $165,000. Individual pay is determined by several factors, which include but are not limited to: job-related skills, experience, and relevant education or training. The range does not include the comprehensive benefits, bonus, long-term incentive, applicable allowances, or any additional compensation that may be associated with this role.
EEO
Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.
If you are qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling 973-307-3550 or by sending an email to ShionogiHR@shionogi.com.
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About Shionogi

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Florham Park, NJ, US

Year founded

2001

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