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.
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.
Scientist II, Process Chemistry
Bristol, PA · On-site
The successful candidate will lead the development, optimization, and scale-up of synthetic ... Preferred * Experience in pharmaceutical, biotechnology, or CDMO environments. * Experience ...
Scientist II, Process Chemistry
Bristol, PA · On-site
The successful candidate will lead the development, optimization, and scale-up of synthetic ... Preferred * Experience in pharmaceutical, biotechnology, or CDMO environments. * Experience ...
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
Quick apply
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... This individual will work closely with Process Development, Analytical Development, MSAT and other ...
S. in Biochemistry, Chemical Engineering, Biotechnology, or related field with 8+ years of relevant industry experience, or * Ph.D. with 4+ years of experience in downstream process development for ...
S. in Biochemistry, Chemical Engineering, Biotechnology, or related field with 8+ years of relevant industry experience, or * Ph.D. with 4+ years of experience in downstream process development for ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
Head of US Quality Assurance
Pennington, NJ · On-site
$190K - $250K/yr
Provide QA oversight for GMP manufacturing, process development, technology transfer, validation ... Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
CABA) is a late-stage clinical biotechnology company focused on developing and launching curative ... Provide analytical expertise to Process Development, Manufacturing Sciences and Technology (MSAT ...
Senior Scientist/Team Leader - Bioprocess Development
King Of Prussia, PA · On-site
$107K - $161K/yr
S. in Biochemistry, Chemical Engineering, Biotechnology, or related field with 8+ years of relevant industry experience, or * Ph.D. with 4+ years of experience in downstream process development for ...
Senior Scientist/Team Leader - Bioprocess Development
King Of Prussia, PA · On-site
$107K - $161K/yr
S. in Biochemistry, Chemical Engineering, Biotechnology, or related field with 8+ years of relevant industry experience, or * Ph.D. with 4+ years of experience in downstream process development for ...
Process SME
Conshohocken, PA · On-site
Maintains current knowledge of relevant developments in their professional area of expertise ... biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and ...
Process SME
Conshohocken, PA · On-site
Maintains current knowledge of relevant developments in their professional area of expertise ... biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and ...
Automation Engineer, GMP
Pennington, NJ · On-site
About ProBio: ProBio, a subsidiary of GenScript, has a one stop biopharmaceutical R&D and ... Biotech Process Equipment/Systems. * Proficient in use of electronic systems, such as Microsoft ...
Automation Engineer, GMP
Pennington, NJ · On-site
About ProBio: ProBio, a subsidiary of GenScript, has a one stop biopharmaceutical R&D and ... Biotech Process Equipment/Systems. * Proficient in use of electronic systems, such as Microsoft ...
Manager of Process Engineering
Philadelphia, PA · On-site +1
... Biotechnology / Pharmaceuticals) team within our Philadelphia office to develop life-changing and ... Participate in Business Development activities including proposal preparation and client ...
Manager of Process Engineering
Philadelphia, PA · On-site +1
... Biotechnology / Pharmaceuticals) team within our Philadelphia office to develop life-changing and ... Participate in Business Development activities including proposal preparation and client ...
Director, Business Development - Development, Northeast (Remote)
West Point, PA · Remote
$142K - $193K/yr
Focus on new client acquisition, identifying new business opportunities with biotech and ... Broad understanding of the discovery and pre-clinical development process. Excellent communication ...
Director, Business Development - Development, Northeast (Remote)
West Point, PA · Remote
$142K - $193K/yr
Focus on new client acquisition, identifying new business opportunities with biotech and ... Broad understanding of the discovery and pre-clinical development process. Excellent communication ...
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
Senior Director, CMC Team Leader
Philadelphia, PA · On-site +1
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
Senior Director, CMC Team Leader
Philadelphia, PA · On-site +1
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
Senior Director, CMC Team Leader
Philadelphia, PA · On-site +1
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
Senior Director, CMC Team Leader
Philadelphia, PA · On-site +1
CABA) is a clinical-stage biotechnology company focused on developing and launching the first ... Develop integrated CMC development plans including process development, analytical development ...
Biotech Process Development information
See Philadelphia, PA salary details
$19.16 - $21.96
3% of jobs
$21.96 - $24.76
6% of jobs
$24.76 - $27.56
12% of jobs
$28.04 is the 25th percentile. Wages below this are outliers.
$27.56 - $30.37
23% of jobs
The median wage is $31.47 / hr.
$30.37 - $33.17
15% of jobs
$33.17 - $35.97
15% of jobs
$37.13 is the 75th percentile. Wages above this are outliers.
$35.97 - $38.77
3% of jobs
$38.77 - $41.57
3% of jobs
$41.57 - $44.37
6% of jobs
$44.37 - $47.17
3% of jobs
$47.17 - $49.97
11% of jobs
$19
$33
$49
How much do biotech process development jobs pay per hour?
What is biotech process development?
What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?
What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?
What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?
| Aspect | Biotech Process Development | Biotech Manufacturing Associate |
|---|---|---|
| Primary Focus | Designing, optimizing, and scaling up bioprocesses for product development | Executing manufacturing processes to produce biopharmaceuticals at scale |
| Work Environment | Laboratories and pilot plant facilities | Production floors and manufacturing plants |
| Required Skills | Process design, lab techniques, troubleshooting | Equipment operation, quality control, adherence to SOPs |
| Typical Credentials | BSc/MSc in Biotechnology, Chemical Engineering, or related fields | BSc 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.
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Cities near Philadelphia, PA with the most Biotech Process Development job openings:

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.Â
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 geneÂ
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 onÂ
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,Â
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. foreignÂ
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 theÂ
- 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 corporateÂ
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 fromÂ
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.Â
- Must possess strong computer skills, including knowledge of databases and spreadsheets and proficiency with Microsoft Office (Word, Excel, PowerPoint, andÂ
Outlook). - Must have strong interpersonal skills, time management, organization, prioritization, planning and coordination, and multi-tasking skills.Â
- 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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