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4D Molecular Therapeutics
Research Associate, Formulation Development (Contract)
Career Insights for Process Development Scientist
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What they do
A Process Development Scientist researches and develops methods for creating and improving chemical manufacturing processes. They may work in a range of industrial sectors, including manufacturing, biotech, and pharmaceuticals. They design experiments, analyze data, and optimize procedures to enhance efficiency, quality, and cost-effectiveness.
$96,298 / year median in California
Job Description
New Research Associate, Formulation Development (Contract) Emeryville, California Apply Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery
GENERAL SUMMARY 4DMT
is seeking a motivated Research Associate, Formulation Development (Contract) to support pre-formulation and formulation development activities for biologic products. This role reports to the Principal Scientist, Process Development. This contract role requires onsite, lab-based work five days per week in Emeryville, California. Primary responsibilities include formulation screening, accelerated stability, forced degradation, material/device compatibility and formulation analytics. Requisites include a B.S. degree, a willingness to learn, good communication skills and a general enthusiasm for science.MAJOR DUTIES & RESPONSIBILITIES
Execute high-throughput, plate-based formulation screening, including formulation preparation, stability studies, sample testing, data analysis, and documentation. Support prefilled-syringe and other container/device compatibility assessments. Formulation analytics including but not limited to Size-Exclusion Multi-Angle Light Scattering, Differential Scanning Fluorimetry, Dynamic Light Scattering, pH and osmo testing. Collaboration with Upstream PD, Downstream PD andAD/QC QUALIFICATIONS
Education:
Bachelors of Science Degree Experience:
0+ years of experience within the Biotech or similar industry Strong foundational laboratory skills, including accurate pipetting, solution preparation, weighing, basic laboratory calculations, and data organization using Excel. Hands-on laboratory experience gained through academic research, internships, or industry. Experience with preformulation, formulation development, stability studies, drug-product process development, or downstream process development is preferred. Experience with biologics, including proteins, antibodies, or AAV/gene therapy, is a plus.Other Qualifications/Skills:
Applicant should possess a general competency in Microsoft based applications (e.g., Word, Excel, PowerPoint) Prior experience with statistical tools (e.g., JMP) or Prefilled Syringe development is preferred, but not requiredTravel:
This role does not require travel outside of the main office. However, may provide opportunities to travel in future (e.g., to attend conferences or oversee outsourced activities)Physical Requirements and Working Conditions:
Physical Activity- Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers.
Fingering:
Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling.Talking:
Expressing or exchanging ideas by means of the spoken word. Physical Requirements- Lifting up to 20 lbs, bending, lifting, twisting, ability to wear Personal Protective Equipment such as lab coat, goggles/glasses, and nitrile gloves Working Conditions
- The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).
Hourly compensation range:
$39.00- $45.
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- Manual pipetting and plate-based sample preparation Buffer, solution, or formulation preparation Pre-formulation or formulation development Stability or forced-degradation studies Drug-product or downstream process development Prefilled-syringe or device compatibility testing HPLC DLS, MALS/SEC-MALS, or DSF None of the above Available Start Date
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Important:
Candidates must be authorized to work in the United States and provide valid work authorization documentation throughout their employment in accordance with U.S. immigration requirements. 4D Molecular Therapeutics welcomes candidates who require nonimmigrant visa transfers or extensions; however, the company does not sponsor new nonimmigrant visa status petitions.- Select... I have reviewed this application personally, and I agree that all statements I have made on this application, in my resume, and other supplementary materials submitted by me are true and correct. I have not knowingly withheld any information that might adversely affect my chance for employment.
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Benefits
- Dental Insurance