Process Development Associate III

Our purpose is to bring hope to life by enabling lifechanging therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.

JOB SUMMARY

This is a Process Development Associate III position in the Downstream Process Development group. This is an exciting opportunity to join our team focused on developing robust and scalable purification processes for monoclonal antibodies and recombinant proteins. The successful candidate will be responsible for designing and executing experiments to optimize protein purification strategies supporting process transfer to cGMP manufacturing and assessing new technologies for downstream processing. Under general supervision this individual will conduct routine to moderately complex experiments analyze data and contribute to process development initiatives.

ESSENTIAL JOB DUTIES/RESPONSIBILITIES

• Development of robust cost effective and wellcharacterized processes for purification of monoclonal antibodies and recombinant proteins.

• Bench scale production to demonstrate process performance.

• Support of process transfer and scaleup into the cGMP manufacturing facility.

• Process validation planning and if required for commercial capabilities.

• Assessment and implementation of new technologies for protein purification and processing.

• Contributes to design of experiments (DoE) and analyzes and interprets experimental results in consultation with supervisor as needed.

• Write protocols client reports and templates with limited supervision.

• Enables downstream process transfer from Process Development labs to Manufacturing.

• Contribute to or conduct continuous lab improvement and management.

• Acts as a resource for less experienced team members and colleagues.

Requirements

• Handson experience with proteins particularly process purification via chromatography and filtrationbased methods. Handson experience with protein characterization and analysis is also a plus.

• Ability to plan experiments analyze and interpret results and move to the next step with periodic supervision. Experience with statistical analysis and experimental design i.e. JMP is an advantage.

• Careful attention to detail in record keeping data analysis and reporting and maintenance of a clean and orderly work area.

• Excellent written and oral communication skills are required as this individual will document results of development work on a daily basis write project reports and potentially participate in meetings and give presentations.

• Good interpersonal skills and a desire to work as part of a team and across teams.

QUALIFICATIONS

• B.S./M.S. degree and 35 years of relevant experience. Equivalent education and experience may substitute for stated requirements.

• Proficiency in protein purification and relevant lab methodologies.

Preferred:

• Previous experience with process development and knowledge of largescale manufacturing activities.

COMPENSATION

$83920 $115390

Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work sidebyside with our clients and partners every step of the way. We provide worldclass development and manufacture of mammalian and microbialbased therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMPcompliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fasttrack projects and rare diseases. AGC Biologics is the partner of choice. To learn more visitwww.agcbio.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.