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Solid Biosciences Inc Jobs (NOW HIRING)

Ideayabio

Senior Patent Agent

South San Francisco, CA · On-site

... Biosciences Inc. will not create any implied obligation. Failure to comply with this policy will ... solid tumor indications. Our mission is to bring forth the next wave of precision oncology ...

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Solid Biosciences Inc information

What does Solid Biosciences Inc do?

Solid Biosciences Inc is a biotechnology company focused on developing therapies for rare neuromuscular and cardiac diseases, with a primary emphasis on Duchenne muscular dystrophy (DMD). The company utilizes innovative gene therapy and precision medicine approaches to address unmet medical needs in these patient populations. Solid Biosciences conducts research, clinical development, and collaborates with partners to advance potential treatments from the laboratory to patients.

What are some common challenges faced by employees working at Solid Biosciences Inc, and how does the company support its teams?

Working at Solid Biosciences Inc., professionals often encounter the challenge of navigating the complexities of drug development in the rare disease space, where timelines can be uncertain and scientific hurdles are significant. The company fosters a collaborative environment, encouraging cross-functional teamwork among research, clinical, and regulatory teams to overcome obstacles. Solid Biosciences Inc. also invests in professional development and open communication, supporting employees through mentorship and regular feedback to help them grow and adapt to evolving project needs.

What are the key skills and qualifications needed to thrive as a biotechnology professional at Solid Biosciences Inc, and why are they important?

To thrive as a biotechnology professional at Solid Biosciences Inc., you need a strong background in molecular biology, genetics, and biochemistry, typically supported by a relevant degree in life sciences. Experience with laboratory techniques (such as PCR, Western blotting, and cell culture), as well as familiarity with data analysis software and regulatory compliance, is highly valued. Attention to detail, problem-solving skills, and the ability to work collaboratively are essential soft skills in this field. These capabilities ensure accurate research outcomes, efficient teamwork, and compliance with industry regulations, which are critical for advancing innovative therapies.

What is the difference between Solid Biosciences Inc vs Solid Biosciences Inc Research Associate?

AspectSolid Biosciences IncSolid Biosciences Inc Research Associate
CredentialsBachelor's or Master's in Life SciencesBachelor's or Master's in related field, some roles prefer lab experience
Work EnvironmentResearch labs, corporate officesLaboratory settings, experimental work
Industry UsageBiotech research and developmentSupporting research projects, data collection, lab experiments

Solid Biosciences Inc is a biotech company focused on gene therapy research, while a Research Associate at Solid Biosciences Inc typically supports research activities within the company. The main difference lies in roles: Solid Biosciences Inc refers to the organization, whereas the Research Associate is a specific position involved in hands-on research tasks.

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Solid Biosciences Inc jobs near you
Infographic showing various Solid Biosciences Inc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Senior Engineer, Oral Solid Dose Packaging Development

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 days ago

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
The Senior Engineer, Oral Solid Dose Packaging Development provides technical leadership for packaging systems supporting assigned products from early clinical development through commercialization and lifecycle management.
The role leads primary packaging engineering & development, packaging material selection, container closure system development, secondary and tertiary packaging. This position partners with Clinical Supply Chain, Packaging Operations, Pharmaceutical Development, Quality, Regulatory Affairs, Supply Chain, external manufacturing sites, testing laboratories, and packaging vendors.
Your Contributions (include, but are not limited to):
  • Lead end-to-end packaging material selection, engineering, and qualification for oral solid dose container closure systems and associated secondary and tertiary packaging, from early clinical development through commercialization and lifecycle management
  • Establish packaging strategies, specifications, critical material attributes, engineering and process controls, and acceptance criteria based on product, stability, patient, packaging, and regulatory requirements
  • Design, execute, interpret, and document packaging development, package integrity, transportation, qualification, and validation studies supporting clinical trial materials and registration stability
  • Lead technical assessments for CPO (contract packaging organization) selection and drive packaging site readiness for commercial launch, including line trials, packaging qualification, process validation, technology transfer, launch execution, and operational handover
  • Lead technical investigations for packaging related deviations, and nonconformances, and retain post launch technical ownership for lifecycle changes, troubleshooting, packaging vendors and CPO transfers, and continuous improvement in partnership with Packaging Operations
  • Lead packaging artwork development, including dielines, component specifications, print requirements, barcodes, serialization product requirements, and packaging line compatibility
  • Author and review regulatory packaging content, including container closure system information, packaging development data, technical justifications, and responses to health authority questions
  • Partner with internal teams and external organizations to deliver packaging programs and evaluate emerging materials, technologies, and sustainability solutions

Requirements:
  • Bachelor's degree in Packaging Science, Packaging Engineering, Materials Science, Mechanical Engineering, Chemical Engineering, Pharmaceutical Sciences, or a related technical field with 4+ years of relevant experience; or Master's degree with typically 2+ years of applicable experience
  • Experience in pharmaceutical packaging development or packaging engineering within a cGMP-regulated environment, with working knowledge of applicable FDA and ICH guidance, USP requirements, and ASTM, ISTA, and ISO standards
  • Direct experience with oral solid dose packaging, including bottle and/or blister packaging systems
  • Experience selecting, developing, and qualifying packaging materials, primary packaging components, and container closure systems, with knowledge of moisture and oxygen barrier properties, light protection, compatibility, mechanical performance, aging, and material variability
  • Experience supporting packaging activities across development and commercial phases, including clinical trial materials, registration stability, regulatory submissions, commercial launch, and lifecycle management
  • Experience authoring and reviewing packaging content for regulatory submissions, including container closure system information, packaging development data, technical justifications, and responses to health authority questions
  • Experience planning and executing packaging development, package integrity, transportation, qualification, and validation studies, engineering and process controls, and acceptance criteria
  • Experience supporting packaging equipment, line trials, technical site assessments, process validation, technical site transfer, packaging related investigations, change controls, and CAPA
  • Strong technical judgment, problem-solving, project management, communication, and cross-functional leadership skills

Preferred Requirements:
  • Six or more years of pharmaceutical packaging development or packaging engineering experience, with demonstrated technical leadership for oral solid dose products
  • Experience independently leading packaging programs from early clinical development through registration, commercial launch, and post-approval lifecycle management
  • Experience with sachet, stick-pack, or flexible-laminate packaging, including material selection, seal development, package integrity, equipment compatibility, and line qualification
  • Experience developing or qualifying parenteral packaging and container closure systems, including vials, stoppers, prefilled syringes, cartridges, or other injectable product configurations
  • Experience developing packaging strategies for moisture-sensitive products, including desiccant systems, high-barrier blister materials, induction sealing, and moisture-protection studies
  • Experience with child-resistant, senior-friendly, tamper-evident, or patient-centered packaging systems
  • Experience leading packaging technology transfers, CPO site readiness, alternate vendor qualifications, or commercial packaging site transfers

#LI-LS1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $97,000.00-$133,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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