Abzena Jobs Hiring Now
Abzena is hiring for 24 open roles on Migrate Mate as of August 31, 2026, concentrated in biotech & life sciences and program management, with listed salaries up to about $180,000. Migrate Mate updates Abzena's live openings daily. Abzena is a contract development and manufacturing organization serving the biotechnology and pharmaceutical industry, supporting biologics and drug conjugate programs through integrated development, manufacturing, and quality services.
Find Abzena JobsOverview
Abzena hiring data on Migrate Mate, as of August 31, 2026.
- Open jobs
- 24
- Top team
- Biotech & Life Sciences
- Seniority
- Mid to senior level
- Work type
- 0% remote or hybrid
- Top location
- Bristol
- Salary range
- $40,000–$180,000
Listed salaries for Abzena roles on Migrate Mate range from about $40,000 to $180,000 per year across 24 open roles, as of August 31, 2026.
Open Roles at Abzena
Showing 24 of 24+ Abzena jobs
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Senior Process Engineer provides advanced process engineering support and technical leadership for GMP manufacturing operations at the Bristol, PA site. Responsibilities include technical leadership of manufacturing campaigns, complex process troubleshooting, technology transfer, process optimization, scale-up, engineering studies, and operational readiness activities.
Reporting to the Director, Process Engineering, the Senior Process Engineer works cross-functionally with Manufacturing, MSAT, Quality, Facilities & Engineering, Supply Chain, and Program Management to support safe, compliant, reliable, and effective manufacturing operations. The role serves as a senior technical subject matter expert, independently leads complex engineering activities, provides technical guidance and mentorship to less experienced engineers, and drives improvements in process performance and reliability within bioconjugation and biologics manufacturing operations.
Responsibilities
Process Engineering & Manufacturing Support
- Provide advanced process engineering support for GMP manufacturing operations including bioconjugation, chromatography, filtration, formulation, and single-use processing systems.
- Provide on-floor technical leadership during manufacturing campaigns, including complex troubleshooting, technical decision support, and issue resolution.
- Partner with Manufacturing and MSAT teams to improve process robustness, throughput, yield, scalability, and execution efficiency.
- Lead technical investigations related to process deviations, operational issues, and adverse process performance trends, including root cause analysis and corrective action development.
- Develop and implement process improvements and engineering solutions that enhance operational reliability and reduce recurring manufacturing risk.
Technology Transfer & Scale-Up
- Lead or serve as the Process Engineering technical lead for technology transfer activities from Process Development into GMP Manufacturing.
- Lead process scale-up assessments, equipment fit evaluations, engineering studies, and manufacturing readiness planning.
- Review and provide technical approval or input for manufacturing records, protocols, technical documents, and process instructions to ensure readiness and technical accuracy.
- Lead or provide technical oversight for process validation, PPQ activities, engineering runs, and process characterization studies.
Technical Leadership & Team Contribution
- Serve as a senior technical resource and mentor to Process Engineers and manufacturing personnel.
- Coach less experienced engineers in troubleshooting, technical writing, investigation methodology, and GMP engineering practices.
- Promote accountability, collaboration, GMP compliance, technical rigor, and continuous improvement across engineering activities.
- Independently prioritize complex engineering work and support the Senior Manager in coordinating technical activities aligned with manufacturing schedules and site objectives.
Quality & Compliance
- Ensure assigned engineering activities are executed in compliance with cGMP regulations, internal procedures, and Abzena quality standards.
- Lead or provide senior technical support for deviations, CAPAs, investigations, change controls, and risk assessments related to process engineering.
- Participate in regulatory inspections and client audits as a technical SME and support preparation of technical responses.
- Drive improvements that reduce repeat deviations, strengthen process consistency, and improve technical control of manufacturing processes.
Operational Excellence
- Analyze process performance metrics, equipment utilization, manufacturing trends, and process capability to identify improvement opportunities.
- Lead Lean and continuous improvement initiatives focused on process efficiency, waste reduction, throughput, and manufacturing effectiveness.
- Develop and implement standardized engineering practices, technical tools, and operational improvements across manufacturing operations.
- Collaborate with Operations leadership to improve schedule adherence, campaign execution reliability, and technical readiness.
Cross-Functional Collaboration
- Partner closely with Manufacturing, MSAT, Quality, Supply Chain, Facilities & Engineering, and Program Management teams.
- Support and, when appropriate, lead client-facing technical discussions related to manufacturing execution, investigations, process performance, and improvement plans.
- Provide technical leadership in campaign planning, operational readiness reviews, and production support activities.
- Identify and escalate significant technical risks, operational constraints, and process concerns to the Senior Manager, Process Engineering with recommended actions.
Qualifications
- Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, Biotechnology, or related scientific discipline required.
- Advanced degree preferred.
- Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
- Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
- Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
- Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
- Experience serving as a technical SME during regulatory inspections or client audits preferred.
- Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
- Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
- Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
- Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
- Experience serving as a technical SME during regulatory inspections or client audits preferred.
Preferred Qualifications
- Experience within bioconjugation, ADC, oligonucleotide, or complex biologics manufacturing environments.
- CDMO experience supporting external clients.
- Experience supporting startup operations or facility expansions.
- Lean Six Sigma or continuous improvement experience preferred.
FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Senior Process Engineer provides advanced process engineering support and technical leadership for GMP manufacturing operations at the Bristol, PA site. Responsibilities include technical leadership of manufacturing campaigns, complex process troubleshooting, technology transfer, process optimization, scale-up, engineering studies, and operational readiness activities.
Reporting to the Director, Process Engineering, the Senior Process Engineer works cross-functionally with Manufacturing, MSAT, Quality, Facilities & Engineering, Supply Chain, and Program Management to support safe, compliant, reliable, and effective manufacturing operations. The role serves as a senior technical subject matter expert, independently leads complex engineering activities, provides technical guidance and mentorship to less experienced engineers, and drives improvements in process performance and reliability within bioconjugation and biologics manufacturing operations.
Responsibilities
Process Engineering & Manufacturing Support
- Provide advanced process engineering support for GMP manufacturing operations including bioconjugation, chromatography, filtration, formulation, and single-use processing systems.
- Provide on-floor technical leadership during manufacturing campaigns, including complex troubleshooting, technical decision support, and issue resolution.
- Partner with Manufacturing and MSAT teams to improve process robustness, throughput, yield, scalability, and execution efficiency.
- Lead technical investigations related to process deviations, operational issues, and adverse process performance trends, including root cause analysis and corrective action development.
- Develop and implement process improvements and engineering solutions that enhance operational reliability and reduce recurring manufacturing risk.
Technology Transfer & Scale-Up
- Lead or serve as the Process Engineering technical lead for technology transfer activities from Process Development into GMP Manufacturing.
- Lead process scale-up assessments, equipment fit evaluations, engineering studies, and manufacturing readiness planning.
- Review and provide technical approval or input for manufacturing records, protocols, technical documents, and process instructions to ensure readiness and technical accuracy.
- Lead or provide technical oversight for process validation, PPQ activities, engineering runs, and process characterization studies.
Technical Leadership & Team Contribution
- Serve as a senior technical resource and mentor to Process Engineers and manufacturing personnel.
- Coach less experienced engineers in troubleshooting, technical writing, investigation methodology, and GMP engineering practices.
- Promote accountability, collaboration, GMP compliance, technical rigor, and continuous improvement across engineering activities.
- Independently prioritize complex engineering work and support the Senior Manager in coordinating technical activities aligned with manufacturing schedules and site objectives.
Quality & Compliance
- Ensure assigned engineering activities are executed in compliance with cGMP regulations, internal procedures, and Abzena quality standards.
- Lead or provide senior technical support for deviations, CAPAs, investigations, change controls, and risk assessments related to process engineering.
- Participate in regulatory inspections and client audits as a technical SME and support preparation of technical responses.
- Drive improvements that reduce repeat deviations, strengthen process consistency, and improve technical control of manufacturing processes.
Operational Excellence
- Analyze process performance metrics, equipment utilization, manufacturing trends, and process capability to identify improvement opportunities.
- Lead Lean and continuous improvement initiatives focused on process efficiency, waste reduction, throughput, and manufacturing effectiveness.
- Develop and implement standardized engineering practices, technical tools, and operational improvements across manufacturing operations.
- Collaborate with Operations leadership to improve schedule adherence, campaign execution reliability, and technical readiness.
Cross-Functional Collaboration
- Partner closely with Manufacturing, MSAT, Quality, Supply Chain, Facilities & Engineering, and Program Management teams.
- Support and, when appropriate, lead client-facing technical discussions related to manufacturing execution, investigations, process performance, and improvement plans.
- Provide technical leadership in campaign planning, operational readiness reviews, and production support activities.
- Identify and escalate significant technical risks, operational constraints, and process concerns to the Senior Manager, Process Engineering with recommended actions.
Qualifications
- Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, Biotechnology, or related scientific discipline required.
- Advanced degree preferred.
- Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
- Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
- Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
- Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
- Experience serving as a technical SME during regulatory inspections or client audits preferred.
- Minimum 6+ years of experience within biopharmaceutical, biologics, bioconjugation, ADC, or CDMO manufacturing environments.
- Demonstrated experience independently supporting GMP manufacturing operations and leading complex process engineering activities.
- Strong experience with technology transfer, process scale-up, process troubleshooting, data analysis, and process optimization.
- Experience leading process validation support, engineering studies, manufacturing investigations, and change implementation.
- Experience serving as a technical SME during regulatory inspections or client audits preferred.
Preferred Qualifications
- Experience within bioconjugation, ADC, oligonucleotide, or complex biologics manufacturing environments.
- CDMO experience supporting external clients.
- Experience supporting startup operations or facility expansions.
- Lean Six Sigma or continuous improvement experience preferred.
FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
Job Roles at Abzena
Working at Abzena
Abzena's 24 open roles are mid to senior level, and about 0% are remote or hybrid. The most active teams are biotech & life sciences, program management, and factory & production work. Abzena is a contract development and manufacturing organization in the biotechnology and pharmaceutical sector, providing integrated services across process development, GMP manufacturing, and quality assurance for biologics and antibody-drug conjugate programs. Most Abzena roles are based in Bristol, with some in San Diego and Carlsbad.
Explore more roles by function
Browse thousands of live openings across engineering, sales, product, and more, and apply in just a few clicks.
Browse jobs by roleAbzena Jobs: Frequently Asked Questions
How many jobs is Abzena hiring for right now?
Abzena is hiring for 24 open roles on Migrate Mate as of August 31, 2026, updated daily, concentrated in biotech & life sciences and program management. Openings span manufacturing operations, process development, quality assurance, and program management functions across Abzena's sites.
What kinds of roles does Abzena hire for?
The most active teams are biotech & life sciences, program management, and factory & production work. Abzena hires across GMP manufacturing, process development science, quality assurance and compliance, engineering, and project and program management. Roles range from associate and technician-level manufacturing positions to senior scientists, engineers, and director-level quality and operations leaders. Most postings are mid to senior level.
Are Abzena jobs remote or in-person?
Mostly on-site. About 0% of Abzena's open roles on Migrate Mate are remote or hybrid as of August 31, 2026, with the rest based in Bristol. Each Abzena listing shows its work location so you can filter before applying.
How do I apply to a job at Abzena?
Find an open Abzena role on Migrate Mate, then follow the listing directly through to Abzena's own careers page to complete the application. Abzena manages its own hiring process, including candidate review, interviews, and offers. Migrate Mate keeps Abzena's postings current so you see live openings without having to search multiple sources.
What do Abzena jobs pay?
Listed salaries for Abzena roles on Migrate Mate range from about $40,000 to $180,000 per year as of August 31, 2026, with most postings at mid to senior level. Exact pay is set by Abzena and shown on each listing.
Does Abzena hire entry-level?
Most of Abzena's open roles on Migrate Mate are mid to senior level as of August 31, 2026. Entry-level openings are limited. Check individual Abzena listings for stated experience requirements.
Where is Abzena hiring?
Most Abzena roles are based in Bristol, with some in San Diego and Carlsbad, and about 0% offer remote or hybrid work as of August 31, 2026. Migrate Mate shows the location on each listing.