Solid Biosciences Jobs Hiring Now
Solid Biosciences is hiring for 6 open roles on Migrate Mate as of August 31, 2026, concentrated in business operations and cloud & DevOps, with listed salaries up to about $329,000. Migrate Mate updates Solid Biosciences's live openings daily. Solid Biosciences is a biotechnology company focused on developing therapies for serious genetic diseases, with research and commercial functions spanning drug discovery, medical affairs, and data science.
Find Solid Biosciences JobsOverview
Solid Biosciences hiring data on Migrate Mate, as of August 31, 2026.
- Open jobs
- 6
- Top team
- Business Operations
- Seniority
- Manager level or above
- Work type
- 67% remote or hybrid
- Top location
- Charlestown
- Salary range
- $125,000–$329,000
Listed salaries for Solid Biosciences roles on Migrate Mate range from about $125,000 to $329,000 per year across 6 open roles, as of August 31, 2026.
Open Roles at Solid Biosciences
Showing 6 of 6+ Solid Biosciences jobs
Associate Director/Director, Technical Quality – Solid Biosciences
Charlestown, MA or Remote (US)
Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care.
Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases.
We are seeking an Associate Director/Director of Technical Quality Assurance to provide strategic and operational leadership over external parties for the assigned program(s) to ensure that all outsourced manufacturing, analytical testing, packaging, labeling, and distribution activities comply with global cGMP, GDP, and regulatory requirements.
This role will report to the Senior Director, Technical Quality and is flexible to be fully remote within the United States or based out of Solid’s Corporate Headquarters in Charlestown, MA.
Key Position Responsibilities
CDMO/CTL Oversight
- Negotiate, execute, and provide oversight of relevant Quality Agreements to ensure compliance.
- Lead Supplier Audits and Qualifications.
- Provide Quality oversight to processes including, but not limited to, technology transfer of processes and analytics, CDMO GMP manufacture, CTL testing, and package/label/distribution of high-quality products for clinical trials building towards commercial.
- Review CDMO manufacturing and testing documentation (batch records, change controls, deviations, etc.) to assess completeness, adequacy, as well as compliance with procedures and applicable regulatory requirements.
- Oversee/approve lot release and disposition for products and starting materials.
- Packaging and labeling oversight ensuring batch records and execution meets requirements.
- Cold chain and distribution compliance including temperature excursion management.
- Implement and lead QP batch certification for EU/UK distribution.
Quality Systems & Compliance
- Establish and track Key Quality Indicators for all outsourced activities.
- Act as QA Lead at joint Solid/Supplier periodic meetings and provide input into governance or other charters.
- Monitor performance in collaboration with functional colleagues and provide input into actions required for improvement.
- Act as an inspection lead and/or liaison for regulatory inspections specific to the program and manage responses to observations.
- Act as QA Lead on cross functional program teams, providing input for regulatory submission packages (pre-IND, IND, IMPD, CTA, BLA, etc.) and other documents as requested.
- Identify risk and evaluate deficiencies, collaborating cross-functionally to remediate risk to an acceptable level.
- Oversee quality and effectiveness of quality system documents and records, i.e., SOPs, change controls/notifications, deviations and CAPAs.
- Lead continuous improvement of the GMP quality management system in collaboration with functional leaders.
- Promote a company-wide culture of quality and collaborate with the quality team on development and implementation of a quality manual and quality policy that supports.
Experience Requirements
- Bachelor’s degree in a science-related field (experience may substitute for degree).
- Minimum of ten years (Associate Director) or fifteen (Director) of direct technical Quality Assurance experience in the biotech industry.
- Strong understanding of GMP Quality for starting and critical raw materials, drug substance, drug product, analytical testing, and label/packaging, and distribution.
- Minimum of three years in a leadership role directly managing outsourced activities (CDMOs/CTLs). Preference for establishment of supplier oversight programs.
- Experience and understanding of Biologics manufacturing processes and analytics, at clinical and commercial stage.
- Strong preference for candidates with previous manufacturing/QC operations experience.
- Strong preference for candidates with previous experience in AAV gene therapy experience.
- Experience with process and analytical tech transfer from one site to another including comparability and bridging requirements.
- Experience bringing a product to commercialization.
- Regulatory agency inspection direct experience is required.
Key Position Attributes
- Ability and desire to work independently and make decisions with minimal supervision in a fast-paced environment.
- Strong collaboration, team-building, and organizational skills.
- Anticipate <10% travel for on-site visits to external suppliers and company meetings
Compensation
The base compensation range for this role is: $190,000.00 – 230,000.00
Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance.
Benefits and Solid Advantages
At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices.
- Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs
- 401(k) program participation with competitive company matched contributions
- Eligibility to participate in Solid’s Employee Stock Purchase Plan
- Mobile phone subsidy for eligible employees
- Tuition Reimbursement
- Vision Coverage
- Life Insurance
- Voluntary Pet Insurance
- Employee Discount Program on Travel, Entertainment, and Services
- Employee Assistance Programs
- Daily Subsidized Lunch Delivery (onsite @ Hood Park)
- Free Onsite Full-Service Gym (onsite @ Hood Park)
- Employee Parking (onsite @ Hood Park)
- 12 Observed Holidays and a winter shut down
- 15-day PTO Policy and a 80-hour rollover YoY
- 40-hour Sick Policy
- 8 Hour Floating Holiday
Associate Director/Director, Technical Quality – Solid Biosciences
Charlestown, MA or Remote (US)
Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care.
Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases.
We are seeking an Associate Director/Director of Technical Quality Assurance to provide strategic and operational leadership over external parties for the assigned program(s) to ensure that all outsourced manufacturing, analytical testing, packaging, labeling, and distribution activities comply with global cGMP, GDP, and regulatory requirements.
This role will report to the Senior Director, Technical Quality and is flexible to be fully remote within the United States or based out of Solid’s Corporate Headquarters in Charlestown, MA.
Key Position Responsibilities
CDMO/CTL Oversight
- Negotiate, execute, and provide oversight of relevant Quality Agreements to ensure compliance.
- Lead Supplier Audits and Qualifications.
- Provide Quality oversight to processes including, but not limited to, technology transfer of processes and analytics, CDMO GMP manufacture, CTL testing, and package/label/distribution of high-quality products for clinical trials building towards commercial.
- Review CDMO manufacturing and testing documentation (batch records, change controls, deviations, etc.) to assess completeness, adequacy, as well as compliance with procedures and applicable regulatory requirements.
- Oversee/approve lot release and disposition for products and starting materials.
- Packaging and labeling oversight ensuring batch records and execution meets requirements.
- Cold chain and distribution compliance including temperature excursion management.
- Implement and lead QP batch certification for EU/UK distribution.
Quality Systems & Compliance
- Establish and track Key Quality Indicators for all outsourced activities.
- Act as QA Lead at joint Solid/Supplier periodic meetings and provide input into governance or other charters.
- Monitor performance in collaboration with functional colleagues and provide input into actions required for improvement.
- Act as an inspection lead and/or liaison for regulatory inspections specific to the program and manage responses to observations.
- Act as QA Lead on cross functional program teams, providing input for regulatory submission packages (pre-IND, IND, IMPD, CTA, BLA, etc.) and other documents as requested.
- Identify risk and evaluate deficiencies, collaborating cross-functionally to remediate risk to an acceptable level.
- Oversee quality and effectiveness of quality system documents and records, i.e., SOPs, change controls/notifications, deviations and CAPAs.
- Lead continuous improvement of the GMP quality management system in collaboration with functional leaders.
- Promote a company-wide culture of quality and collaborate with the quality team on development and implementation of a quality manual and quality policy that supports.
Experience Requirements
- Bachelor’s degree in a science-related field (experience may substitute for degree).
- Minimum of ten years (Associate Director) or fifteen (Director) of direct technical Quality Assurance experience in the biotech industry.
- Strong understanding of GMP Quality for starting and critical raw materials, drug substance, drug product, analytical testing, and label/packaging, and distribution.
- Minimum of three years in a leadership role directly managing outsourced activities (CDMOs/CTLs). Preference for establishment of supplier oversight programs.
- Experience and understanding of Biologics manufacturing processes and analytics, at clinical and commercial stage.
- Strong preference for candidates with previous manufacturing/QC operations experience.
- Strong preference for candidates with previous experience in AAV gene therapy experience.
- Experience with process and analytical tech transfer from one site to another including comparability and bridging requirements.
- Experience bringing a product to commercialization.
- Regulatory agency inspection direct experience is required.
Key Position Attributes
- Ability and desire to work independently and make decisions with minimal supervision in a fast-paced environment.
- Strong collaboration, team-building, and organizational skills.
- Anticipate <10% travel for on-site visits to external suppliers and company meetings
Compensation
The base compensation range for this role is: $190,000.00 – 230,000.00
Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance.
Benefits and Solid Advantages
At Solid Biosciences we offer a highly competitive total rewards and benefits package, intended to support all aspects of our employees’ lives and well-being. Additionally, for those employees working onsite at our Hood Park Headquarters, we offer a variety of onsite resources to support those working in our offices.
- Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs
- 401(k) program participation with competitive company matched contributions
- Eligibility to participate in Solid’s Employee Stock Purchase Plan
- Mobile phone subsidy for eligible employees
- Tuition Reimbursement
- Vision Coverage
- Life Insurance
- Voluntary Pet Insurance
- Employee Discount Program on Travel, Entertainment, and Services
- Employee Assistance Programs
- Daily Subsidized Lunch Delivery (onsite @ Hood Park)
- Free Onsite Full-Service Gym (onsite @ Hood Park)
- Employee Parking (onsite @ Hood Park)
- 12 Observed Holidays and a winter shut down
- 15-day PTO Policy and a 80-hour rollover YoY
- 40-hour Sick Policy
- 8 Hour Floating Holiday
Job Roles at Solid Biosciences
Working at Solid Biosciences
Solid Biosciences's 6 open roles are manager level or above, and about 67% are remote or hybrid. The most active teams are business operations, cloud & DevOps, and business development. Solid Biosciences is a biotechnology company working on genetic medicine, with functions spanning scientific research, regulatory and commercial affairs, biostatistics, and medical communications. The company hires across roles in drug discovery, translational development, analytical development, and global market strategy. Most Solid Biosciences roles are based in Charlestown and Remote.
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Browse jobs by roleSolid Biosciences Jobs: Frequently Asked Questions
How many jobs is Solid Biosciences hiring for right now?
Solid Biosciences is hiring for 6 open roles on Migrate Mate as of August 31, 2026, updated daily, concentrated in business operations and cloud & DevOps. Positions range from scientist-level research roles to executive and senior director leadership across scientific, commercial, and medical functions.
What kinds of roles does Solid Biosciences hire for?
The most active teams are business operations, cloud & DevOps, and business development. Solid Biosciences posts roles across drug discovery, translational and analytical development, medical affairs, biostatistics, data science, scientific communications, and commercial strategy. Legal and executive leadership positions also appear regularly. Most postings are manager level or above, reflecting the company's focus on experienced specialists and senior functional leaders.
Are Solid Biosciences jobs remote or in-person?
Mostly remote. About 67% of Solid Biosciences's open roles on Migrate Mate are remote or hybrid as of August 31, 2026, with the rest based in Charlestown. Each Solid Biosciences listing shows its work location so you can filter before applying.
How do I apply to a job at Solid Biosciences?
Find a role that fits your background on Migrate Mate, then follow the listing through to Solid Biosciences' own careers page to submit your application directly. Solid Biosciences manages its own hiring process, including application review, interviews, and offers. Migrate Mate keeps Solid Biosciences's listings current so you're seeing active openings.
What do Solid Biosciences jobs pay?
Listed salaries for Solid Biosciences roles on Migrate Mate range from about $125,000 to $329,000 per year as of August 31, 2026, with most postings at manager level or above. Exact pay is set by Solid Biosciences and shown on each listing.
Does Solid Biosciences hire entry-level?
Most of Solid Biosciences's open roles on Migrate Mate are manager level or above as of August 31, 2026. Entry-level openings are limited. Check individual Solid Biosciences listings for stated experience requirements.
Where is Solid Biosciences hiring?
Most Solid Biosciences roles are based in Charlestown and Remote, and about 67% offer remote or hybrid work as of August 31, 2026. Migrate Mate shows the location on each listing.