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Subject Matter Expert - Protein Therapy

Remote / Online - Candidates ideally in
Walkersville, Frederick County, Maryland, 21793, USA
Listing for: Lonza
Full Time, Remote/Work from Home position
Listed on 2026-02-16
Job specializations:
  • IT/Tech
    Data Security
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Subject Matter Expert - Protein Based Therapy
Location: Walkersville

United States, Walkersville (Maryland)

Subject Matter Expert - Protein Based Therapy Location

This is a fully remote position. The ideal candidate is based in a major life sciences hub such as San Francisco or the Boston area. The role requires 40–50% travel.

What You Will Get

The full-time base annual salary for this position is expected to range between $144,000 to $244,000. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus.
  • Medical, dental and vision insurance.
  • 401(k) matching plan.
  • Life insurance, as well as short-term and long-term disability insurance.
  • Employee assistance programs.
  • Paid time off (PTO).

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What You Will Do

The Subject Matter Expert (SME) – Protein Based Therapy serves as the technical authority for Lonza’s bioprocessing portfolio, playing a critical role in enabling customer success and driving commercial growth. This role partners closely with Business Development, Account Management, and cross-functional teams to deliver deep scientific, product, and process expertise across the sales cycle. Acting as a trusted advisor to both customers and internal stakeholders, the SME helps translate complex technical challenges into scalable, compliant solutions that accelerate the development and commercialization of protein-based therapies.

  • Lead the technical strategy for complex sales opportunities in partnership with Account Managers and Business Development Managers to improve win rates and mitigate technical and regulatory risk.
  • Serve as the technical authority in customer engagements, including workshops, troubleshooting sessions, product demonstrations, and proof-of-concept projects.
  • Prioritize technical support activities based on revenue potential, strategic importance, and risk.
  • Deliver advanced technical and application training to internal sales teams, distributors, and key customers.
  • Coach and mentor commercial teams on technical positioning, application differentiation, and objection handling.
  • Investigate and resolve escalated technical and product performance issues using root-cause-driven, sustainable solutions.
  • Act as a trusted technical partner to strategic customers to support product adoption, expansion, and long‑term success.
  • Collaborate cross‑functionally with Marketing, Product Management, R&D, Quality Assurance, Service, and Regulatory Affairs to ensure solutions are technically sound, compliant, and scalable.
  • Translate customer feedback, application needs, and competitive intelligence into structured insights for Product Management, R&D, and Marketing.
  • Support new product launches by shaping technical messaging, application positioning, and sales enablement materials.
  • Review and contribute to technical documentation, white papers, application notes, and competitive analyses.
  • Build and maintain relationships with key opinion leaders and regulatory authorities.
  • Present technical data, application concepts, and market insights at industry conferences, customer meetings, and internal forums.
  • Perform other duties as assigned.
What We Are Looking For
  • Bachelor’s degree required; master’s degree or PhD preferred in Biotechnology, Biochemistry, Chemical Engineering, or a related life sciences discipline.
  • Extensive hands‑on experience working with GMP‑regulated products and environments.
  • Strong background in protein‑based therapeutics, including development, scale‑up, and commercialization.
  • Demonstrated experience in mammalian cell culture process development, including upstream and/or downstream processing.
  • Solid understanding of bioprocess development workflows, from early development through clinical and commercial manufacturing.
  • Proven experience supporting or leading technology transfer activities, including transfer of processes from development to manufacturing or between sites and external partners.
  • Ability to assess process robustness, scalability, and risk across different stages of the product lifecycle.
  • Expert technical mastery of bioprocessing tools, technologies, and applications relevant to…
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