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Added 8 hours ago
Healthcare Analytics QA Lead – Value-Based Care Platform
Jobgether
Remote, United States
The Healthcare Analytics QA Lead will oversee end-to-end quality assurance for a healthcare analytics platform integrating clinical, claims, and payer data to support value-based care…
Added 2 days ago
A
Director, Engineering, Technical Expert Sterile Fill
AbbVie
Durham, NC
- $160,500 to $305,000 USD / year
Partner with Quality, MS&T, Validation / CQV and Operations to ensure aseptic process simulations, media fill strategy, filter integrity testing, sterile filtration, container closure…
Added 2 days ago
A
Director, Engineering, Technical Expert Sterile Fill
AbbVie
Remote, United States
- $160,500 to $305,000 USD / year
Partner with Quality, MS&T, Validation / CQV and Operations to ensure aseptic process simulations, media fill strategy, filter integrity testing, sterile filtration, container closure…
Added 3 days ago
Sr.Software Dev Engineer, DDB Index and Search
Amazon.com Services LLC
Seattle, WA
As an SDE III, you will own significant technical decisions and carry them through implementation, validation, launch, and production operation. You will lead designs spanning component…
Added 3 days ago
Senior Specialist, Global Engineering Solutions (GES)
Merck
Rahway, NJ
Lead and collaborate with contractors, suppliers and other team members in the execution of the work, ensuring adherence to the GES Project Roadmap for capital project execution.
Added 3 days ago
Lead Data Engineer
Empower Retirement, LLC
Remote, United States
Lead technical execution of complex data initiatives across teams, translating business requirements into scalable data solutions.
Added 5 days ago
Lead Engineer - Filtration Materials
Mann+Hummel GmbH
Gastonia, NC
MANN+HUMMEL is seeking a highly motivated and innovative Lead Engineer - Filtration Materials to serve as a technical expert in raw materials, material performance, and durability. This…
Added 5 days ago
Lead Engineer - Filtration Materials
United States
MANN+HUMMEL is seeking a highly motivated and innovative Lead Engineer - Filtration Materials to serve as a technical expert in raw materials, material performance, and durability. This…
Added 8 days ago
A
Senior Aseptic Process Engineer
Actalent
Baltimore, MD
- $100 to $125 USD / hour
The Aseptic Process Engineer will lead the technical evaluation, design, and implementation of improvements to legacy aseptic filling and setup practices, with a strong focus on reducing…
Added 9 days ago
Guidance Navigation & Control Engineer III-IV
Kratos Defense & Security Solutions, Inc.
Arlington, TX
Control system gain and filter design and stability margin evaluation.
Added 10 days ago
VT
Engineer, Sterile Drug Product
VIKING THERAPEUTICS INC
San Diego
- $200,000 to $220,000 USD / year
…drug product manufacturing, technology transfer, and process validation activities across Viking Therapeutics’ pipeline. Working within Technical Operations and in close partnership with…
Added 11 days ago
Manager I, Engineering - Reference Tables Access
Datadog
NY · Boston, MA
…Tables lets them use their own reference data to enrich and filter observability data without leaving the platform. The team also owns the table identity, metadata, permissions, quotas,…
Added 11 days ago
RU
Manufacturing Technician III - Sterile Filling (Day Shift)
Resilience US, LLC
West Chester, OH
- $24 to $38 USD / hour
Perform and execute filter integrity testing as needed per SOP.
Added 12 days ago
Fraud Operations Manager
Citigroup
San Antonio, TX
Manage an advanced Fraud Operations team's performance and execution
Added 12 days ago
Filter Validation Execution Lead
Sanofi Group
Swiftwater, PA
The Filter Validation Execution Lead is responsible for designing and executing development and validation studies for sterilizing-grade filters, virus filtration filters, bioburden…
Added 13 days ago
Director, Property & Casualty Staff Underwriting
Nationwide Mutual Insurance Co.
Remote, United States
Underwriting rules: Lead the strategic development, implementation, governance, and ongoing management of underwriting rules, guidelines, and related control gaps.
Added 13 days ago
Engineering Program Manager, Powersports
Gates Co
Denver, CO
…is the designated responsible individual, owner, and go to lead for the global program(s) they are leading. EPMs facilitate good communication and offer multiple levels of status across a…
Added 15 days ago
Senior Program C&Q Lead
Lilly
Richmond, VA
The Senior Program C&Q Lead owns commissioning and qualification (C&Q) for an assigned capital program or site – setting the C&Q strategy, driving field execution, and delivering systems…
Added 15 days ago
Fraud Operations Manager
Citigroup
San Antonio, TX
Manage an advanced Fraud Operations team's performance and execution
Added 15 days ago
Senior Program C&Q Lead
Lilly
Houston, TX
The Senior Program C&Q Lead owns commissioning and qualification (C&Q) for an assigned capital program or site – setting the C&Q strategy, driving field execution, and delivering systems…
Added 16 days ago
Senior Program C&Q Lead
Lilly
Huntsville, AL
The Senior Program C&Q Lead owns commissioning and qualification (C&Q) for an assigned capital program or site – setting the C&Q strategy, driving field execution, and delivering systems…
Added 16 days ago
SP
Chief Engineer
Systems Planning and Analysis
Colorado Springs, CO
- $200,000 USD / year
…assessments, systems engineering and integration, test, planning and execution, cost estimating and analysis, acquisition support, and cybersecurity. We are trusted partners developing…
Added 16 days ago
Senior Program C&Q Lead
Eli Lilly and Company
United States
The Senior Program C&Q Lead owns commissioning and qualification (C&Q) for an assigned capital program or site – setting the C&Q strategy, driving field execution, and delivering systems…
Added 17 days ago
Senior Program C&Q Lead
Eli Lilly and Company
United States
The Senior Program C&Q Lead owns commissioning and qualification (C&Q) for an assigned capital program or site – setting the C&Q strategy, driving field execution, and delivering systems…
Added 17 days ago
Development Technologist or Research Technician, Rotational Program
Locus Biosciences
Research Triangle Park, NC
…including set-up and operation of development-scale bioreactors, filter trains, tangential flow filtration (TFF) equipment, and chromatography…

Locus Biosciences

Development Technologist or Research Technician, Rotational Program

Research Triangle Park, NC, United States

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Job details

Education: Master’s degree
Posting language: English
Posted: Jul 23, 2026

Original job description

Locus Biosciences is seeking a highly motivated and entrepreneurial applicant to join our company in a full-time, entry-level position that will rotate between our Chemistry, Manufacturing and Controls (CMC) and Research & Development (R&D) departments during this 2 year rotational program. This position is well suited for those looking for an entry-level position that is excited to learn all aspects of biotechnology drug development from early-stage research through drug product manufacturing. Candidates will be expected to accomplish defined work, as well as assist in approaching and solving complex scientific problems. Candidates should have demonstrated laboratory or manufacturing experience, with solid communication, technical aptitude, and problem-solving skills. Experience working in regulated, pharmaceutical/biotechnology R&D (GDP, GLP) and/or manufacturing environments (cGMP) is strongly preferred, but not required. Why Locus?

Change the future of medicine and address a serious and unmet patient need by developing completely novel therapeutic modalities.
Fast-track your career by tackling large & meaningful projects and learning a breadth of techniques and skillsets in the wet lab and manufacturing suites
Work with a team of exceptionally talented and hardworking individuals while striving to achieve a common mission
Partner with the most highly respected pharmaceutical companies in the world
Bonus pool eligibility
Health, dental, vision, life insurance, 401(k), and PTO
Free access to fitness center and classes

Responsibilities will include:

Designing and/or executing formulation development activities
Designing and/or executing bench-scale process development activities, including set-up and operation of development-scale bioreactors, filter trains, tangential flow filtration (TFF) equipment, and chromatography equipment
Development of analytical strategies to inform formulation and process development activities
Design and deploy automated workflows for molecular biology and microbiology assays, including liquid handling automation, next-generation sequencing (NGS) library preparation, and high-throughput screening of phage activity to accelerate research timelines and improve experimental reproducibility.
Support the development of data infrastructure and bioinformatics pipeline for R&D and CMC operations, including DNA sequence analysis, sequence assembly, and comparative genomic analysis.
Molecular biology and synthetic biology– Cloning, NGS library preparation, characterization of novel genetic engineering tools, and generation and analysis of novel engineered phage clones
Microbiology – Culturing both aerobic and obligate anaerobic organisms. Utilizing a range of bacterial strains to produce and characterize activity of phage
Independent management, planning, and execution of multiple projects, including reviewing, interpreting, and recording results.
Supporting tech transfer of new products and processes to ensure smooth transition from R&D to process development to GMP manufacturing
Forming strong relationships with all stakeholders, including technicians, associates, project and program managers, and scientists to enable successful tech transfer
Supporting Scientists in all aspects of pharmaceutical development
Assisting in the preparation of batch records, protocols, SOPs, deviations, technical reports, presentations, and other CMC documents to support drug development, including INDs, BLAs, and other applications
Gaining aseptic gowning and fill qualification
Performing material handling and staging
Practicing real-time documentation (such as batch records) during production run and maintain accurate records/logs according to GDP
Supporting Qualification and Validation activities
Identifying, communicating, and troubleshooting process issues
Supporting team effort in the effective and timely completion of root cause investigations and CAPA
Supporting a high-performance teamwork environment

Rotations may include a combination of any of the following functions:

Research and Development including but not limited to phage discovery, phage engineering, and strain engineering.
High Throughput Development (Automation)
Bioinformatics
Material Sciences & Technology
cGMP Manufacturing
Analytical Development
Quality Control
Clinical Lab
Quality Assurance
Project Management Office
Clinical Operations

Education:

Technical certificate or degree (e.g. BTEC Biomanufacturing), or graduation from an accredited college/university with a Bachelor’s to a Master’s degree in Biology, Chemistry, Biochemistry, Chemical Engineering, Biophysics, Pharmaceutical Technology or related field, with some lab experience (required)

Experience and Expertise:

Familiarity with general laboratory techniques such as pipetting, serial dilutions, aseptic technique and proper decontamination procedures
Experience in research, pharmaceutical, biotechnology, and/or sterile production environment
Experience executing SOPs and documenting work
Strong mechanical aptitude
Excellent oral and written communication skills
Technical writing ability
Thrives in a fast-paced, entrepreneurial and collaborative environment. Openly shares knowledge/information needed to accomplish a task or solve a problem

Preferred Qualifications:

At least two years’ experience between academic or industry research
Experience in biologics (upstream, downstream, aseptic fill/finish) with working knowledge of FDA regulations and GMP systems
Experience with DNA sequence analysis, including homology searching, sequence assembly and primer design
Ability to assist in the design of experiments and interpretation of results
Motivation to learn new processes that contribute to the company's overall desire to get products into the clinic
Technical proficiency with designing and executing standard molecular biology experiments (PCR, transformation, Gibson cloning)
Experience with microbiology skills like growth curves, anaerobic microbiology, streaking and banking strains

*The level of the position will be based on the successful candidate’s qualifications.

About Locus Biosciences Locus Biosciences is a clinical-stage biotechnology company developing precision antibacterial products to address critical unmet medical needs in treating bacterial infections and microbiome indications. The Locus platform engineers bacterial viruses called bacteriophages to specifically kill target pathogens while leaving non-target bacteria (i.e., the rest of the patient’s microbiome) unharmed and to deliver biotherapeutic payloads to the body sites where they are needed. Locus’s lead program is an engineered bacteriophage product targeting Escherichia coli bacteria in the urinary tract, currently being tested in an active Phase 2/3 clinical trial. Locus has collaborations with BARDA and CARB-X to develop engineered bacteriophage products targeting E. coli infections and Klebsiella pneumoniae infections, respectively. For more information about Locus visit https://www.locus-bio.com/ SHIFT: Full-Time Days, with occasional evening and weekend work Job Type: Full-time, onsite Job Location: Research Triangle Park, North Carolina Direct applicants only. No agencies please.

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More about this job

Skills

Research
Communication skills
Problem solving
Biotechnology
Molecular biology
Assembly
Genetic engineering
Good manufacturing practices
Presentation skills
Material handling
Documentation
Troubleshooting
Teamwork
Quality control
Quality assurance
Project management
Microsoft Office
Chemical engineering
Pharmaceutical technology
Laboratory techniques
Technical writing

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