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Biotech Process Development Jobs in Philadelphia, PA

Maintains current knowledge of relevant developments in their professional area of expertise ... biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and ...

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Biotech Process Development information

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$19

$33

$49

How much do biotech process development jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for biotech process development in Philadelphia, PA is $33.99, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $41.73 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are popular job titles related to Biotech Process Development jobs in Philadelphia, PA?

For Biotech Process Development jobs in Philadelphia, PA, the most frequently searched job titles are:

What job categories do people searching Biotech Process Development jobs in Philadelphia, PA look for?

The top searched job categories for Biotech Process Development jobs in Philadelphia, PA are:

What cities near Philadelphia, PA are hiring for Biotech Process Development jobs?

Cities near Philadelphia, PA with the most Biotech Process Development job openings:

Infographic showing various Biotech Process Development job openings in Philadelphia, PA as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 17% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $70,697 per year, or $34 per hour.

Patent Counsel/Senior Patent Counsel

Philadelphia, PA • Hybrid

Full-time

Posted 6 days ago


Job description

Legend Biotech is seeking a Patent Counsel/Senior Patent Counsel as part of the Legal team based in either Philadelphia, PA or Somerset, NJ. 

Role Overview

Legend Biotech's Intellectual Property team is seeking a Patent Counsel/ Senior Patent Counsel with large molecule expertise, including antibody and process development experience. Experience in cell and gene 
therapy and gene therapy platforms is a plus. As a partner and business strategist, this individual contributor will push the boundaries of what is possible in a highly competitive industry. This position reports directly to the Global Head of Intellectual Property in Legend's Legal Department. Come join our passion for creating IP strategies that will enable Legend to improve the lives of patients worldwide. This is a hybrid position (currently 3 days a week). There is expected to be some travel between Legend Headquarters in Bridgewater NJ and Legend's R&D locations in Philadelphia PA and Somerset, NJ.

Key Responsibilities

  • Driving strategic IP procurement and management of global intellectual property, including drafting and prosecuting patent portfolios, working with outside counsel, and serving as a key legal partner on 
    business development, licensing, collaboration, acquisition, and other strategic transactions. 
  • Responsibilities include supporting IP-focused due diligence, evaluating transaction-related risks and opportunities, advising on intellectual property strategy, and conducting freedom-to-operate, 
    infringement, validity, and risk assessment and mitigation analyses.
  • Managing the prosecution of active global dockets, including handling U.S. and foreign patent applications as well as post-grant proceedings (e.g., reexamination, reissue, post-grant review. foreign 
    oppositions and appeals), as necessary.
  • Rendering due diligence assessments, freedom-to-operate, infringement, and validity analyses, and risk evaluation and mitigation strategies.
  • Identifying and exploiting new strategic opportunities and approaches by leveraging a deep understanding of patent law and a knowledge of the competitive landscape.
  • Partnering effectively with relevant stakeholders at all levels and of the global Legend organization and across all phases of research, development, and commercialization to provide clear, strategic business enabling strategies.
  • Influencing business leaders as a trusted advisor and thought partner.
  • Deploying in-depth patent and scientific expertise to provide education, guidance, and advice on patent law issues to scientists conducting research and other business stakeholders.
  • Maintaining and sharing expertise and knowledge on legal case law, rules, or regulations before the 
  • U.S. Patent and Trademark Office as well as other relevant jurisdictional IP offices.
  • Reviewing, drafting, and negotiating intellectual property provisions in a broad range of commercial, research, development, manufacturing, collaboration, licensing, and other corporate agreements to ensure alignment with Legend's intellectual property strategy and business objectives.
  • Supporting business development, licensing, collaboration, and other strategic transactions by conducting IP diligence, assessing intellectual property assets and risks, and advising on transaction structure and intellectual property strategy.
  • Partnering in intellectual property-related transactions, adverse proceedings, and litigation activities related to individual's program responsibilities.
  • Participating in group, department, and cross-functional projects and initiatives where strategies, processes, operating standards, and/or practices are developed and deployed to ensure highest quality practices and execution for all aspects of IP portfolios in a high performing, agile team setting.
  • Sustainably building enduring, productive external relationships with outside counsel, third-party collaborators, and partners.

Requirements

  • Minimum requirements: Undergraduate degree in the biological sciences with focus on immunology, cell biology, cancer biology, biochemistry, and the like. Preference given to those with advanced degrees. Admission to practice before the U.S. Patent and Trademark Office (USPTO) required. U.S. law degree (J.D.)
  • 8+ years of patent attorney experience in life sciences patent prosecution, with majority of experience in patent application drafting and prosecution in a pharma/biotech corporate 
    setting and/or representing such clients/matters in a law firm.
  • Admission to practice before the U.S. Patent and Trademark Office (USPTO) required.
  • A current "good standing" admission to at least one U.S. state bar is required.
  • Building and leveraging global IP portfolios for biopharmaceuticals at all stages of prosecution and enforcement;
  • Designing and executing complex freedom-to-operate analyses across different technologies and different jurisdictions.
  • Developing and communicating actionable risk mitigation strategies;
  • Experience supporting business development, licensing, collaboration, and other strategic transactions, including intellectual property due diligence, risk assessment, and negotiation of intellectual property-related agreement provisions, is preferred.
  • Experience in adverse IP proceedings, including but not limited to US litigation, is a plus.
  • Experience in gene therapy, cell therapy, and RNA therapeutics is a plus.
  • Exhibits poise under pressure, solution-oriented mindset, clear communication at all levels of an organization, effective collaboration across local and global teams, and active in-person presence with IP/Legal and business stakeholders.
  • Tackles new challenges with curiosity and a growth-mindset, effectively utilizing available resources, and an enthusiastic willingness to listen and learn from 
    others.
  • Excels in working independently and proactively with minimal direction, strong organizational skills, and ability to prioritize and balance competing projects and responsibilities in a fast-paced global organization.
  • Must have a demonstrated capacity to manage and prioritize multiple tasks and to work efficiently and independently in a deadline-driven, high-volume.
  • Must be highly detail-oriented and have excellent oral and written communications skills. 
  • Must possess strong computer skills, including knowledge of databases and spreadsheets and proficiency with Microsoft Office (Word, Excel, PowerPoint, and 
    Outlook).
  • Must have strong interpersonal skills, time management, organization, prioritization, planning and coordination, and multi-tasking skills. 
  • Must demonstrate an ability to build relationships and work as a team player.
  • Must be able to maintain the integrity of confidential and sensitive information in a professional manner.
  • Embraces a growth-mindset and enjoys working in a fast-paced and diverse global organization.
  • Engages actively in Group, Department, and cross-functional projects and initiatives where strategies, processes, operating standards and/or practices are developed and deployed, to ensure the highest quality IP portfolios in a high performing, agile team setting.
  • Embraces and fosters a team and organizational culture that reflects a commitment to diversity, equity, and inclusion.
  • Organization, attention to detail, and analytical abilities.
  • Proactive, self-disciplined and able to work independently with minimal supervision.

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