Work with us

We are on a mission to address today’s — and tomorrow’s — toughest infections. We are looking for intelligent and motivated people to help us reach those goals.

APT’s facilities in Gaithersburg MD are a short thirty minute drive to the beautiful monuments and museums of Washington DC.

What I love about APT is the collaborative environment. All members of the team are more than willing to help another out, creating a family-like environment where everyone is supported.” Marty Lee, Microbiologist II

“APT allows me to strengthen my qualities as a scientist and a team-worker. Such a collaborative environment propels the success of the company and my growth as an individual. Notably, working at APT has introduced me to avenues of science that were previously unknown, broadening my mind to the bigger picture of the biotech industry.” Bryce Walker, Microbiologist I

Working at APT and living around the Frederick/Gaithersburg area has opened my eyes to all that Maryland has to offer! I enjoy the close proximity to Seneca State Park and several other recreational activities. Being a short drive from downtown Frederick and venues like the RIO Washingtonian area allow me to keep engaged in my social (covid-friendly) life in the biotech corridor!” Viet Dang, Microbiologist II

< “We build therapies to clear multidrug resistant infections, with the end goal being to produce as many therapies as possible that have the potential to save lives. Having the opportunity to see that our hard work really does pay off and it’s making a difference right now, that’s unique to Adaptive Phage Therapeutics.“  Bri’Anna Horne, Clinical Coordinator/Microbiologist

Working at APT is like working with family. Coming into work every day, you get to say hello and talk to everyone from the higher executives to the microbiologists in the lab. The open communication really fosters a sense of community, learning, and passion for the work that we are doing. Not only that but, the value of our work is immeasurable – we get the chance to actually see the impact we have on patients and have a direct and lasting effect on each and every person.” Anjna Nair, Microbiologist I

Who we are

APT is a group of seasoned veterans coupled with crazy smart biologists and engineers working to solve the problem of antibiotic resistant infections.  Each day is different and at the end of the day, you’ve made a difference in someone’s life.  It’s incredibly powerful when you meet somebody whose life you impacted by going to work.  The work will challenge you and reward you professionally and personally.  

World-class activities, shopping, and dining are close at hand in the heart of Maryland’s BioTech corridor.

APT was named “The Emerging Life Science Company of the Year” in 2020 by the Maryland Technology Council

Working with us

Headquartered in Gaithersburg, MD, APT is in the heart of the Maryland’s BioTech corridor.  The area offers a great lifestyle with Baltimore 30 miles to the east and Washington 20 miles to the south. There are professional sports, great outdoor spaces, world recognized chefs and restaurants and excellent schools to name just a few opportunities to ensure work-life balance.

We offer competitive salaries and benefits to all employees as well as opportunities for investment and growth. Hiring from within is part of our makeup as well as continued education opportunities.

Open positions:

Position Description: Quality Assurance Associate

Exciting opportunity for an experienced Quality Assurance (QA) Associate to join the QA Department at Adaptive Phage Therapeutics, Inc (APT). In this position, the candidate will guide personnel involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements, and industry best practices.

Major responsibilities:

  • Interface with functional groups, such as Manufacturing and Quality Control (QC) to determine events (errors, deficiencies, discrepancies, deviations, and other observations) and report to management. 
  • Review batch production records and related production documentation, ensuring resolution of all identified issues prior product disposition. Work with internal functions to address all identified issues in a timely manner. Reports errors, deficiencies, discrepancies, and observations to management. 
  • Oversee revision, development and tracking of controlled documents 
  • Initiate and participate in standard operating procedure (SOP) revisions to improve compliance. 
  • Create and revise SOPs, batch records, CAPAs, deviations QA on the floor activities
  • Assist with distributing tracking numbers for the quality systems 
  • Manage databases used for tracking of GMP/GDP documentation
  • Performs QA On-the-Floor activities supporting projects, including room release, auditing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing. 
  • Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and industry best practices. 
  • Review and dispositions executed batch records and supporting documentation for completeness, accuracy, and compliance. 
  • Act as first responder for on the floor quality issues in a timely manner, documentation of all events/investigations and required immediate corrective actions.
  • Works with supervisory staff and department leads in meeting project deliverables in a compliant and efficient manner 

Job requirements:

  • A Bachelor’s Degree in Science, Engineering, or a related technical discipline. 
  • 2+ years’ experience within the biologic, biopharmaceutical, or regulated pharmaceutical industry 
  • 1+ years’ experience in Quality Assurance/Quality Control function 
  • Experience with electronic batch records or LIMS  
  • Familiarity with Good Manufacturing Practices (GMPs) and a working knowledge of cGMP regulations
  • Prior experience and ability to work in an aseptic processing environment. 
  • Experience working in an early phase pharmaceutical manufacturing facility highly desired
  • Strong interpersonal and attention to detail skills
  • Experience working with all Microsoft Office products (Teams, Excel, Word) 

Compensation: Salary is industry-standard and is commensurate with experience.

To apply: Please email cover letter and resume to [email protected]

Job ID: 21.005

Position Description:  Next Generation Sequencing Technician

Exciting opportunity for a junior-level technician to learn Next Generation Sequencing (NGS) and join the Product Development team at Adaptive Phage Therapeutics (APT). The successful candidate will mainly be responsible for DNA extraction and purification from microbiological organisms but will also assist with DNA library preparation for NGS projects using Oxford Nanopore’s long-read sequencing platform. 

Major responsibilities:

  • Follow Standard Operating Procedures (SOPs) and execute laboratory techniques which may include but are not limited to the following: cell culture, DNA extraction and purification, NGS DNA sequencing, PCR, gel electrophoresis, and other common microbiological and molecular biology techniques.
  • Troubleshoot and adjust scientific methodology to correct problems or deficiencies as needed.
  • Maintain careful laboratory records including written lab notebooks and well-organized digital data files.
  • Manage laboratory supply inventory and report deficiencies to supervisor as needed.
  • Adhere to all SOPs and project schedules set by supervisor(s).
  • Provide daily project updates to supervisor(s).
  • Coordinate efforts with data analysis teams as well as management ensuring the business needs are met.

Job requirements:

  • Associate’s or Bachelor’s degree in Biology, Life Sciences, or a related discipline.
  • One (1) year of academic or industrial laboratory experience (non-specific).
  • One (1) year of previous bacterial cell culture and molecular biology laboratory experience is a plus, but not required.
  • Demonstrated knowledge of maintaining accurate and detailed records.
  • Demonstrated knowledge of proper laboratory disposal methods and safety procedures.
  • Ability to adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing and quality processes.
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes. 
  • Must maintain a clean working environment including participation in a regular laboratory cleaning schedule per established cleaning Standard Operating Procedures.
  • Cell culture and/or molecular laboratory experience is a plus.
  • Careful, detail-oriented working style.
  • Outstanding communication, collaboration, and problem-solving skills.

This full-time position reports to the Director, Product Development.

Compensation:  Salary is industry-standard and commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.006

Position Description: Microbiologist I/II – Upstream Production

Exciting opportunity for an experienced microbiologist/phage biologist to join the upstream manufacturing team at Adaptive Phage Therapeutics (APT). In this position, the candidate will work alongside the upstream production team to amplify bacteriophages on host bacterial cultures in mid-scale batches to be used in a clinical setting.

Major responsibilities:

  • Grow bacterial batch culture and amplify bacteriophages in batch cultures including working with single use disposable bioreactor systems.
  • Perform in-process testing of material prior to releasing to downstream manufacturing team(s).
  • Propagate, maintain, and catalogue bacterial cell and bacteriophage lines used for manufacturing of the therapeutic drug product.
  • Perform processes for the manufacture of the therapeutic product(s) under approved Standard Operating Procedures (SOPs).
  • Adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing processes.
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes.
  • May perform QC testing of the therapeutic product per regulatory guidelines and/or SOPs.
  • May help in the ongoing development of scale up batch culture processes.
  • Must maintain a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.

Job requirements:

  • BS in biology or related field.
  • 1 – 2 years of experience in a laboratory setting, prefer experience in microbiology and/or bacteriophage biology.
  • GMP experience preferred.
  • Must be able to lift 40 lbs.
  • Must be able to stand and work for extended periods of time.
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. Weekend shifts are also possible.
  • Outstanding organizational and communication skills.
  • Ability to work independently and as part of a team
  • Self-motivation, adaptability, and a positive attitude

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 2020-004

Position Description:  Microbiologist I/II – Quality Control Testing

Exciting opportunity for an experienced microbiologist/phage biologist to join the upstream manufacturing team at Adaptive Phage Therapeutics (APT). In this position, the candidate will support day-to-day operations to ensure timely and accurate testing of materials and products while maintaining quality and compliance to meet the demands of manufacturing.

Major responsibilities:

  • Support manufacturing operations by; including but not limited to process validation, environmental monitoring, and utility systems sampling and testing.
  • Receive, archive and process clinical trial specimens according to company SOPs.
  • Perform in-house microbiological assays for manufactured material and/or clinical trial samples.
  • Prepare analytical lab reports or summaries as required within the necessary timeframe.
  • Write, revise, and review SOPs for compliance with respective compendia, equipment operation, methods, and general laboratory procedures as needed.
  • Perform in-process testing of material prior to releasing to downstream manufacturing team(s). 
  • Perform processes for the manufacture of the therapeutic product(s) under approved Standard Operating Procedures (SOPs).  
  • Adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing processes. 
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes.
  • Perform QC testing of the therapeutic product per regulatory guidelines and/or SOPs.
  • Must maintain a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.
  • Perform routine quality control review of manufacturing documents to comply with documentation practices outlined in the FDA’s guidance’s for Phase 1 GMP’s. These documents including but are not limited to: SOPs, Batch Records, Forms and third-party testing reports. 
  • Help provide oversight of day to day record-keeping, reporting and daily review according to cGMP guidelines.  
  • Assist with document control of all active and retired Master documents according to the QMS.

Job requirements:

  • BS in biology or related field.
  • 1 – 2 years of experience in a laboratory setting, prefer experience in microbiology and/or bacteriophage biology.
  • GMP experience preferred.
  • Must be able to lift 40 lbs.
  • Must be able to stand and work for extended periods of time.
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. Weekend shifts are also possible. 
  • Outstanding organizational and communication skills.
  • Ability to work independently and as part of a team
  • Self-motivation, adaptability, and a positive attitude

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 2020-006

Position Description:  Microbiologist I/II – Quality Control

Exciting opportunity for an experienced microbiologist/phage biologist to join the upstream manufacturing team at Adaptive Phage Therapeutics (APT). In this position, the candidate will work alongside the upstream production team to perform QC testing of the therapeutic product per regulatory guidelines and/or SOPs including but not limited to: endotoxin quantification, HCP analysis, potency, visual inspection, and stability.

Major responsibilities:

  • Grow bacterial batch culture and amplify bacteriophages in batch cultures including working with single use disposable bioreactor systems. 
  • Perform in-process testing of material prior to releasing to downstream manufacturing team(s). 
  • Propagate, maintain, and catalogue bacterial cell and bacteriophage lines used for manufacturing of the therapeutic drug product.
  • Perform processes for the manufacture of the therapeutic product(s) under approved Standard Operating Procedures (SOPs).  
  • Perform QC testing of the therapeutic product per regulatory guidelines and/or SOPs.
  • Perform routine quality control review of manufacturing documents to comply with documentation practices outlined in the FDA’s guidance’s for Phase 1 GMP’s. These documents including but are not limited to: SOPs, Batch Records, Forms and third-party testing reports.
  • Adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing processes. 
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes.
  • May help in the ongoing development of scale up batch culture processes.
  • Must maintain a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.
  • Help provide oversight of day-to-day record-keeping, reporting and daily review according to cGMP guidelines.  
  • Assist with document control of all active and retired Master documents according to the QMS.

Job requirements:

  • BS in biology or related field.
  • 1 – 3 years of experience in a laboratory setting, prefer experience in microbiology and/or bacteriophage biology.
  • GMP experience preferred.
  • Must be able to lift 40 lbs.
  • Must be able to stand and work for extended periods of time.
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. Weekend shifts are also possible. 
  • Outstanding organizational and communication skills.
  • Ability to work independently and as part of a team
  • Self-motivation, adaptability, and a positive attitude

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.003

Position Description: Microbiologist I/II – Downstream Production

Exciting opportunity for an experienced microbiologist/phage biologist to join the downstream manufacturing team at Adaptive Phage Therapeutics (APT). In this position, the candidate will work alongside the downstream production team to purify batches of bacteriophage from host contaminants in to be used in a clinical setting. 

Major responsibilities:

  • Grow bacterial batch culture and amplify bacteriophages in batch cultures including working with single use disposable bioreactor systems. 
  • Perform in-process testing of material throughout the manufacturing process. 
  • Propagate, maintain, and catalogue bacterial cell and bacteriophage lines used for manufacturing of the therapeutic drug product.
  • Perform processes for the manufacture and purification of the therapeutic product(s) under approved Standard Operating Procedures (SOPs).  
  • Adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing processes. 
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes.
  • May perform QC testing of the therapeutic product per regulatory guidelines and/or SOPs.
  • May help in the ongoing development of scale up production/purification processes.
  • Must maintain a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.

Job requirements:

  • BS in biology or related field.
  • 1 – 2 years of experience in a laboratory setting, prefer experience in microbiology and/or bacteriophage biology.
  • Experience in the operation of downstream equipment such as depth filtration, TFF, and chromatography in a GMP environment is preferred.
  • Must be able to lift 40 lbs.
  • Must be able to stand and work for extended periods of time.
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. Weekend shifts are also possible. 
  • Outstanding organizational and communication skills.
  • Ability to work independently and as part of a team
  • Self-motivation, adaptability, and a positive attitude

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected] 

Job ID: 2020-014

POSITION DESCRIPTION: Downstream Manufacturing Technician

We are looking for an experienced manufacturing technician to join the downstream manufacturing team at Adaptive Phage Therapeutics (APT). In this position, the candidate will work alongside the purification team to purify batches of bacteriophage and perform in-process testing of material through the manufacturing process. The candidate must be comfortable with machinery, equipment, aseptic processing/gowning, and interacting with software interfaces.

Major Responsibilities:

  • Perform downstream processing procedures of bulk drug material according to APT’s Standard Operating Procedures (SOPs).
  • Operate standard processing equipment such as but not limited to: peristaltic pumps, pipettes, tube welders, filtration systems, and liquid handlers.
  • Be comfortable learning new methodologies and skills rapidly while maintaining critical thinking to improve processes and documentation. 
  • Construct/modify existing flowpaths for alternative uses. 
  • Prepare analytical lab reports or summaries as required within the necessary time frame. 
  • Perform in-house microbiological assays for manufactured material and/or clinical trial samples.
  • Document all manufacturing activities clearly and accurately per cGMP, QMS, and regulatory requirements.
  • Adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes.
  • Perform daily manufacturing tasks per SOPs and Manufacturing Production Records.
  • Follow recipes to prepare appropriate reagents for processing according to the approved for the manufacturing process.
  • Perform all production activities in an aseptic, safe, and compliant manner.
  • Routinely monitor manufacturing processes and recognizes potential process issues as they arise; proactively escalate identified issues to senior staff.
  • Ensure continued flow of production activities by assessing item availability and obtaining pertinent material if low on stock.
  • Must maintain a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.

Job Requirements:

  • 2+ year(s): Experience in a regulated cleanroom or manufacturing environment or an Associate degree in a life science field
  • Experience with downstream laboratory techniques (column chromatography, filtration) preferred
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. 
  • Working knowledge of Microsoft Office programs. 
  • Outstanding organizational and technical communication skills. 
  • Ability to work independently and as part of a team.
  • Self-motivation, adaptability, positive attitude, and the ability to multitask while under pressure.
  • Must be able to lift at least 40 pounds. 
  • Must be able to stand and work for extended periods of time. 

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.001

Position Description: Curator/Bioinformatician

Exciting opportunity for experienced bioinformatician/curator to join the team at Adaptive Phage Therapeutics (APT). APT is seeking a highly motivated individual skilled in viral/bacteriophage biology, bacterial genomics and pathogenicity, knowledgeable about wet bench sequencing operations and experienced in curation and analysis of annotated genomic data sets.  The successful candidate will integrate with the current team of biologists and computer scientists.

Responsibilities:

  • Analyze computational analysis of various genomic data sets using common bioinformatics tools, techniques, and pipelines.
  • Improve sequence data quality, classification, and annotation based on bioinformatic analysis, appropriate scientific literature, and through direct communication with scientists.
  • Develop/execute production procedures for analyzing genome data in a regulated environment.
  • Work with data management colleagues to distribute data, monitor processing queues and contribute to workflow improvements.
  • Coordinate project tasks as a member of the data management team.
  • Provide analysis, reports, and recommendations to senior leadership
  • Work with scientists and informatics colleagues to inventory, store and catalog available data for prioritized projects and studies.
  • Maintain content of internal knowledge sharing and documentation repositories.
  • Coordinate with internal stakeholders and external business partners.

Skills:

  • Outstanding communication, collaboration, and problem solving
  • Familiarity working in a Linux environment
  • Familiar with bioinformatics tools/software
  • Programming/scripting/database experience a plus (Python, bash, SQL, unix)
  • Careful, detail-oriented working style
  • Well organized
  • Initiative in suggesting and executing process improvements
  • Innate curiosity

Requirements:

  • Experience with sequence analysis and bioinformatics software
  • Strong problem solving and analytic skills
  • Master’s degree or Ph.D. in Biology, Life Sciences, or a related discipline.
  • Three (3) to Five (5) years of experience in computational biology
  • Examples of software projects/analysis completed
  • Knowledge of/experience with the various sequencing technologies a plus

The position reports to the Director, Product Development

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.007

Position Description: Computational Biologist

Exciting opportunity for capable biologist with experience in bioinformatics to join the team at Adaptive PhageTherapeutics (APT). The role includes preparing samples for DNA sequencing, managing complex biological data sets, analyzing DNA sequences, and producing reports for senior management. The successful candidate will mainly be responsible for DNA extraction and purification from microbiological organisms but will also assist with DNA library preparation for NGS projects using Oxford Nanopore’s long-read sequencing platform. 

Major responsibilities:

  • Follow Standard Operating Procedures (SOPs) and execute laboratory techniques which may include but are not limited to the following: cell culture, DNA extraction and purification, NGS DNA sequencing, PCR, gel electrophoresis, and other common microbiological and molecular biology techniques.
  • Perform computational analysis of various genomic data sets using common bioinformatics tools and pipelines.  Use tools including but not limited to: SPAdes, CLC Genomics Workbench, RAST, Glimmer, Genemark, PGAP
  • Coordinate project tasks as a member of the data management team.
  • Troubleshoot and adjust scientific methodology to correct problems or deficiencies as needed.
  • Maintain careful laboratory records including written lab notebooks and well-organized digital data files.
  • Manage laboratory supply inventory and report deficiencies to supervisor as needed.
  • Adhere to all SOPs and project schedules set by supervisor(s).
  • Draft and update SOPs when necessary.
  • Provide daily project updates to supervisor(s).
  • Coordinate efforts with data analysis teams as well as management ensuring the business needs are met.

Job requirements:

  • Bachelor’s or Master’s degree in Biology, Life Sciences, or a related discipline.
  • Three (3) to Five (5) years of experience in genomics and microbiology.
  • Demonstrated knowledge of maintaining accurate and detailed records.
  • Demonstrated knowledge of proper laboratory disposal methods and safety procedures.
  • Ability to adhere to the company Quality Management System (QMS) to maintain highly controlled manufacturing and quality processes.
  • Ability to adhere to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all Manufacturing/Laboratory processes. 
  • Must maintain a clean working environment including participation in a regular laboratory cleaning schedule per established cleaning Standard Operating Procedures.
  • Careful, detail-oriented working style.
  • Outstanding communication, collaboration, and problem-solving skills.
  • Programming experience a plus

This full-time position reports to the Director, Product Development.

Compensation:  Salary is industry-standard and commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.009

Position Description: Clinical Data Manager

Exciting opportunity for experienced Clinical Data Manager to join the team at Adaptive Phage Therapeutics, Inc. (APT). The Clinical Data Manager will be responsible for data management activities for research studies. This position is responsible for the electronic database design and management including data verification, data cleaning, and quality assurance for multiple projects. 

Major responsibilities:

  • Participates in the design and/or development of study-specific Case Report Forms (CRFs), ensuring consistency with study protocol
  • Collaborates with the project team and other study personnel to determine data collection requirements based on the study protocol and system knowledge 
  • Oversees the design of an electronic data capture (EDC) system to mitigate risk while ensuring the cleanliness of clinical data collection 
  • Documents and resolves data management issues specific to a protocol 
  • Assists with communication for internal and external teams to resolve data management issues
  • Creates or reviews data validation check specifications 
  • Prepares data reports and assists with data presentations as applicable 
  • Identifies and resolves data queries and discrepancies. Contributes to data quality metrics for a protocol or project 
  • Creates and maintains data management documents per SOP (e.g. Data Management Plan, User Acceptance Testing Plan, Data Entry Guidelines, etc.) 
  • Oversees query resolution to verify data quality on regular basis and communicate with clinical team to expedite resolution of queries as well to improve quality of data being collected 
  • Organize and maintain clinical study databases and documents to support regulatory submissions to the FDA
  • Supervises contracted clinical research organizations with the design, build and reporting of data from clinical studies

Job requirements:

  • Bachelor’s Degree in health and/or healthcare informatics, clinical, biological or mathematical sciences or related field or equivalent experience. 
  • Minimum of 5 – 7 years direct data management experience with at least 2 years as a clinical data management project lead. 
  • Previous experience managing the delivery of multiple projects through the full data management life cycle. 
  • Thorough knowledge of the data management process (e.g., serious adverse event reconciliation, management of local laboratory data) and knowledge of data management operating procedures. Knowledge of clinical research regulations including Good Clinical Practices and relevant regulatory guidelines. 
  • Working knowledge of clinical research operations, clinical trials, medical terminology, and/or pharmacology
  • Experience developing clinical trial databases in a commercially available EDC system (e.g. RedCap Cloud, OpenClinica, Medrio, Veeva or Medidata Rave)

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 2020-013

Position Description: Banking Manufacturing Technician 

Exciting opportunity for a microbiologist/phage biologist to join the team at Adaptive Phage Therapeutics (APT). The candidate will work within the Bio Banking Department and may also have opportunity to work across other manufacturing departments. 

Major responsibilities:

  • Propagate, maintain, and catalogue bacterial cell and bacteriophage lines under approved standard operating procedures (SOPs).
  • Adheres to the company Quality Management System (QMS) to maintain highly controlled manufacturing process. 
  • Adheres to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), Biological Safety Level-2 (BSL-2), and aseptic technique in all manufacturing/Laboratory processes.
  • Prepares raw materials and/or equipment for manufacturing and laboratory processes and participates in the inventory auditing.
  • Maintains a clean working environment including participation in regular laboratory cleaning schedule per established cleaning SOPs.

Job requirements:

  • BS in biology or related field.
  • 0-1 years of experience in a laboratory setting, prefer experience in microbiology and/or bacteriophage biology.
  • Will require scheduling flexibility to accommodate varying manufacturing schedules. Weekend shifts are also possible. 
  • Outstanding organizational and communication skills.
  • Proven experience as a team player
  • Must be able to lift 40 lbs.
  • Must be able to stand and work for extended periods of time.

Compensation:  Salary is industry-standard and is commensurate with experience.

To apply:  Please email cover letter and resume to [email protected]

Job ID: 21.004

Don’t see what you are looking for? Think you would be a good fit for our company? Contact us! We will be growing in the coming years and need the right people to help us do that now.

Equal Opportunity Employer

APT is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. APT seeks to diversify its work force and is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. At APT, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our therapeutics, and our community.