Location (mandatory): Marlborough, MA 01752 (Onsite) The engineer will be responsible for leading customer engagements, troubleshooting, running experiments, and analyzing data using techniques such as electrochemistry, SEM, and HPLC. The role involves close collaboration with global teams, preparing technical reports, and ensuring strict adherence to safety protocols.

Location (mandatory): Portsmouth, New Hampshire Responsible for the dispensing of raw materials liquids and powders (hazardous and non-hazardous), acids/bases, under cGMP conditions to support the manufacture of therapeutic proteins (API) Individuals will be required to perform and monitor all dispensing processes and weighs, including liquid, powder (hazardous and non-hazardous), acids and bases. All processes will be completed per cGMP guidelines to support the manufacture of therapeutic proteins (API).

As an experienced scientist, you will need to work independently and efficiently on Synthetic Biology including gene and oligo design, oligo synthesis, gene assembly, next generation sequencing and data analysis, nucleic acid purification and characterization, take lead in high throughput gene synthesis and plasmid production, process automation and protocol development, improvement of quality and throughput, problem solving etc.

Location - South San Francisco, CA 94080. Cell Line Development Research Associate is involved in the creation of stable cell lines for the recombinant adeno-associated viral vector (rAAV) production processes. He/she executes experiments, produces relevant documentation, and works under supervision. He/she will be responsible for: Culturing mammalian cells for viral production in shake flasks, spinner flasks, spin tubes, deep well and automation platforms. Performing experiments in the development, optimization and scale-up of AAV producer cell lines. Preparing process development protocols, data analysis summaries, technical reports, and other relevant process documentation. Optimization of transfection and transduction protocols for newly engineered cell lines. Maintaining an accurate laboratory notebook. Ensuring work conforms to applicable quality and safety standards. Participating on project teams (as needed). Must be able to lift 25 pounds. Due to the inherent nature of cell culture, some weekend work and/or work on holidays may be needed. On occasion, long work hours may be required depending upon the experiment schedule. Handling large volumes of cell culture or related materials, such as tens of liters, may be required. Also, several viral materials, including AAV, may be involved in the work.

Location (mandatory): Greenwood SC 29646 Looking for a entry level candidate with a degree in science

With limited supervision, QC Analyst II, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, QC Associate II works to meet departmental and organizational goals.

Location : Marlborough, MA 01752. • We are seeking a motivated Laboratory Technician to support formulation, chemical processing, and photolithography experiments in our fabrication laboratory. • The ideal candidate will have hands-on chemistry or chemical engineering experience, strong attention to detail, and a commitment to safety.

Location : Belvidere, NJ 07823. • The QC Analyst is responsible for analyzing and testing raw materials, intermediates, stability samples, and finished products under cGMP guidelines using validated or compendial methods. • The role involves performing laboratory analysis with minimal supervision, preparing reagents and standards, calibrating and operating instruments (HPLC, GC, ICP, etc.), and maintaining accurate documentation. • The analyst supports product release testing, investigates out-of-specification results, and ensures compliance with safety, quality, and regulatory standards. • Candidates should hold a degree in a relevant scientific discipline, have 0–3 years of laboratory experience, and demonstrate knowledge of quality control techniques, GMP, and safety practices. • Flexibility to work shifts, overtime, and weekends is required. • 0-3 years of lab experience • Experience in Microsoft Office (outlook, word, and excel) • The schedule may be structured with a required overtime component built in. • Candidates must be able to work shifts, weekends, overtime (including coverage) and holidays as required. • All candidates, both internal and external, applying for this position understand that overtime may be required and adjusted based on business needs and to ensure continued safe operations. Position content- • Key areas of accountability/responsibility • Performs analysis in the laboratory with minimal supervision. • Prepares standards, mobile phases, and reagents. • Calibrates and monitors laboratory equipment (HPLC, GC, ICP, etc.) • Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods. • Performs calculations, collects and prepares data for evaluation. • Keeps supervisor informed of work status • Investigation of OOS results under guidance of senior staff • Maintains good documentation practices.

Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.