Director, External & CMC Quality Assurance
$200k - $260kScholar Rock
Scholar Rock is delivering muscle-targeted breakthroughs to transform the treatment of spinal muscular atrophy (SMA) and other rare neuromuscular diseases where muscle atrophy remains a critical unmet need. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the biopharmaceutical company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more about our neuromuscular franchise at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: Scholar Rock is seeking an experienced and motivated Director of Quality Assurance to support External and CMC Quality Assurance. This role will provide oversight of external partner (Contract Organization) governance for the manufacturing, testing, and release of biological products. This position will work cross-functionally with the CMC teams (Manufacturing, QC, MSAT, etc) and the external partners. This role is responsible for managing quality system records (change control, deviations, product complaints, batch disposition, etc.) and quality risk management to deliver product for clinical and/or commercial purposes. This role will also be responsible for advancing a strong quality culture for proactive issue identification and a state of inspection readiness. This position reports to the Sr. Director, External & CMC Quality Assurance. Position Responsibilities Provide Quality Assurance oversight over Drug Substance manufacturing of GxP biological product. This involves oversight of multiple CMOs as part of a complex supply chain that includes contract laboratories and other critical service providers. Provide QA oversight of deviations, investigations, CAPAs, change controls, testing, product impact assessments, and disposition-related decisions. Design and maintain a robust, scalable product disposition program for clinical trial material as well as commercial products across multiple markets. Ensure continuous inspection readiness across outsourced operations and support health authority inspections, partner inspections, and due diligence activities. Monitor partner quality performance through defined metrics, scorecards, and governance forums; identify trends and proactively upscale compliance or execution risks. Partner cross-functionally to assess quality risk associated with process changes, deviations, investigations, comparability activities, tech transfer, and supply continuity issues. Provide strategic guidance on quality requirements for product lifecycle activities, including clinical supply, commercial readiness, distribution, complaints, and post-approval changes. Drive a culture of quality, accountability, and proactive issue identification across internal stakeholders and external partners. Candidate Qualifications BS/MS degree in a scientific discipline. 12+ years of experience in the pharmaceutical/biotech industry (including meaningful experience in outsourced/virtual operating models), with 5+ years in leadership roles within Quality or related functions Strong working knowledge of GMP/GxP requirements, FDA/EMA expectations, ICH guidance, and risk-based quality management principles. Demonstrated success overseeing external manufacturers, testing laboratories, suppliers, and quality service providers. Experience supporting biologics products across both clinical and/or commercial stages; demonstrated success driving continuous improvement. Strong communication skills, sound scientific judgement, and the ability to balance strategic thinking with hands‑on execution. Highly proactive, decisive, and capable of independently managing key initiatives in a fast‑paced commercial readiness and launch environment. Engaged leader committed to building a strong quality culture through collaboration and mentorship. $200,000 - $260,000 a year Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. #J-18808-Ljbffr Scholar Rock
$135.46k - $203.19k
Job Title: Associate Director, External QualityLocation: Boston, MA Hybrid 3 days/weekFusion Pharmaceuticals... ...pipeline of RCs.The Role:AD, External Quality - Radio Conjugates is accountable for... ...Contribute to regulatory submissions (CMC quality sections) and post-approval...SuggestedFull timeContract workTemporary work$147.5k - $221.3k
Job DescriptionGeneral Summary:The Associate Director, CMC Quality Compliance and Inspection Readiness, is responsible for inspection readiness and compliance of external sites including evaluating, improving, and monitoring commercial level quality compliance and quality...SuggestedFull timeSummer workRemote workFlexible hours2 days per week$147.5k - $221.3k
...Pharmaceuticals seeks an Associate Director to lead inspection readiness and compliance programs for external manufacturing sites. The role... ...collaboration to evaluate quality compliance, drive continuous improvement... ...field ~8+ years of relevant CMC quality or compliance...Suggested$193.1k - $289.7k
Job DescriptionGeneral Summary:The CMC Statistics Director (Scientific Fellow) provides strategic and... ...verification (CPV), stability, quality control, and regulatory submissions. This... ...industry trends. We seek talent who bring an external perspective, demonstrate curiosity and...SuggestedFull timeSummer workRemote workFlexible hours2 days per week- ...Associate Director overseeing external quality for radio conjugate manufacturing partners, CDMOs, and suppliers at Fusion Pharmaceuticals (AstraZeneca). Accountable for ensuring compliance with cGMP, regulatory commitments, and company standards across drug substance,...Suggested
$161.5k - $218.5k
OverviewThe Associate Director, Downstream, Emerging Modalities, is expected... ...Concept transition by leading CMC team as necessary for the... ...strategy across internal and external teams and work closely with... ...Regulatory, Technical Operations, Quality, and CDMO partners to...Full timeTemporary workLocal areaFlexible hours$143k - $233k
...assigned Chemistry, Manufacturing and Control (CMC) programs. Your Role: With minimal... ...and within multi-disciplinary internal and external teams at third parties.Ability to... ...authoring/review/providing CMC content for CMC/quality submissions including IND and IMPD development...$172.2k - $233k
...experienced leader to serve as Associate Director, CMC Technology Delivery to lead the digital... ...(ReDev) and Technical Operations & Quality (TOQ) Technology organization.As a recognized... ...status reportingPartner with CMC, external Contract Manufacturing Organization (CMO...Full timeContract workTemporary workLocal areaFlexible hours3 days per week$166.4k - $249.6k
...The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC... ..., reviewing, and delivering high-quality regulatory submissions, while serving... ...industry trends. We seek talent who bring an external perspective, demonstrate curiosity and...Full timeSummer workRemote workFlexible hours2 days per week- ...Kymera Therapeutics seeks a Director or Senior Director to manage chemistry... ...submission support, and CMC strategy for programs advancing... ..., drug product, analytical, quality, regulatory, and supply chain... ...decisions to stakeholders and external partners Coordinate CMC documentation...
$184.6k - $277k
...DescriptionGeneral/Position SummaryThe Director, Manufacturing Process & Technical Quality provides Quality leadership and... ..., Supply Chain, Regulatory, and external partners, the Director ensures alignment... ...supporting a site, program, CMC, or R&D leadership team strongly preferred...Full timeSummer workRemote workFlexible hours2 days per week$154.4k - $242.55k
...Chemistry Manufacturing & Controls (CMC) and Devices organization, and... ...issues to key internal and external colleagues, including Alliance... ...with HA regulations. Assures conformance with Takeda controlled... ...Analytical Development, Production, Quality Assurance can be considered)....Minimum wageLocal areaRemote workWorldwide$156.6k - $234.8k
...Manufacturing Process & Technical Quality Associate Director provides end-to-end l... ...as a Quality Assurance Subject Matter Expert (SME)... ...Quality representative on CMC Governance forums to ensure... ...manufacturing operations and external contract manufacturing organizations...Full timeContract workSummer workRemote workFlexible hours2 days per week$136.51k - $204.77k
...Job Title: Associate Director, CMC Lead Introduction to role: Are you ready to lead early... ...guide and contribute to authoring high-quality documentation and data packages for IND... ...and effective collaboration with external partners or CDMOs. Understanding of...Hourly payTemporary work$172k - $202k
...resourceful, and enthusiastic quality control lead excited to be a... ...commercial stage. You will work with CMC technical SMEs, QA and... ...development, quality Assurance, Regulatory, and CRO/CDMOs. Your... ...activities both internally and externally related to safety, identity,...Work at officeLocal areaRemote work1 day per week$258.33k - $280k
...unique opportunity for a seasoned quality systems professional who... ...systems across QA, Clinical Ops, CMC, and Research, ensuring... ...ecosystem of internal and external vendors-ranging from eQMS and... ...biotech/pharma Quality Assurance, with direct ownership of...Remote work3 days per week$195k - $330k
...How you’ll make an impact:Drive end-to-end CMC program management for mid to late-stage... ...substance, drug product, analytical, quality, regulatory, and supply chain workstreams... ...required with 10+ years of CMC experience; Sr. Director level requires commensurate additional...- ## Associate Director, Regulatory Affairs CMCApplyremote type: Site Basedlocations... ...patients. As the Regulatory CMC lead for these programs, you... ...teams, and with relevant external parties including contract... ...plan, prepare, and submit high-quality CMC related applications...Contract workRemote work
$177k - $278.08k
...entrepreneurial mind-set. Role Purpose AIRx executes the majority of its wet-lab work externally — its speed, cost, and quality targets all depend on CROs operating as a true extension of the team. The Director, AIRx CRO & External Partnerships is the single accountable owner of all...Minimum wageFull timeContract workLocal areaRemote work$200k - $240k
Associate Director of External Communications (Litigation)Cooley is seeking an Associate Director of External Communications for Litigation to join theCommunicationsteam.Position summary: Working closely with the Director of Communications, firm leadership, the broader...Full timeTemporary workWork at officeImmediate startFlexible hoursWeekend work$171.2k - $256.8k
...of Boston, Massachusetts.SummaryThe Director, GCP & GLP QA, reporting to the Executive Director, Quality, is responsible for leading quality assurance oversight across clinical and nonclinical... ...QA guidance to internal teams and external partners. It’s an exciting time to...Contract work- Johnson & Johnson Innovative Medicine seeks a Director of Oncology External Innovation to advance external partnerships and pipeline opportunities across oncology. You will lead cross-functional diligence, shape scientific strategies, and collaborate with Janssen Oncology...Worldwide
- PineTree Therapeutics in Cambridge, MA, seeks a Director of Developability and Early CMC Development to lead analytical method development, developability assessment, and cell line development for monoclonal and multispecific antibodies. You will oversee CRO/CDMO collaborations...
- Takeda in Cambridge, MA is seeking a director-level leader to identify, evaluate, and advance external innovation opportunities in AI, automation, data, and digital technologies that can accelerate drug discovery. This role reports to the Head of External Portfolio Innovation...Work at office2 days per week3 days per week
$164k - $282.9k
...finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at The Director, Oncology External Innovation will be responsible for identifying opportunities and implementing the external innovation plan of...Local areaImmediate startRemote workWorldwide- ...Vertex Pharmaceuticals seeks a CMC Statistics Director to lead statistical strategy across the product lifecycle, from process development through... ...-making, and partner across development, manufacturing, quality, and regulatory teams to enhance product quality and...
$94.6k - $141.8k
Job DescriptionGeneral Summary:The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced technical resource responsible... ...and providing timely quality direction in support of external drug substance manufacturing and disposition.Key Duties...Full timeContract workSummer workRemote workFlexible hours2 days per week$156.6k - $234.8k
...DescriptionGeneral Summary:The Associate Director, GMP Operational Quality is responsible for oversight of team... ...and application of quality assurance and compliance. The incumbent is responsible... ...VertexCollaborate with internal and external business partners to resolve complex...Full timeWork experience placementSummer workRemote workFlexible hours2 days per week$185k - $225k
...serious diseases.Position Overview:We are seeking an Associate Director, Quality Control to lead the Beam Massachusetts Quality Control team... ...inspections, health authority interactions, and internal/external audits by ensuring QC records, SMEs, laboratory systems, and...Full time$185k - $225k
...patients suffering from serious diseases.Position Overview:The Associate Director of Product Quality Assurance (PQA) will be responsible for phase appropriate quality oversight of internal and external manufacturing and analytical activities. These activities include...Full timeContract workWorldwide
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