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Project Controls Manager (Wind Renewables Construction)
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Remote, United States
- $120,000 to $160,000 USD / year
…all applications and next steps. Our partner is looking for a Project Controls Manager (Wind Renewables Construction) based in the United…
Added 23 mins ago
Construction Manager
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- $7.25 USD / hour
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Added 3 hours ago
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…five consecutive years, we specialize in program management, project controls, commissioning, and technology - and offer an excellent platform to grow your career while shaping the future…
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Sales Engineer
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- $90,000 to $120,000 USD / year
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Added 5 hours ago
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- $110,000 to $140,000 USD / year
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Added 5 hours ago
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DevSecOps Engineer (Kubernetes, CI/CD)
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Added 5 hours ago
Director of Finance and Accounting
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ARS Pharmaceuticals Operations, Inc.

Manager / Senior Manager, Technical Operations

San Diego, CA, United States

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Job details

Posting language: English
Posted: Oct 31, 2026

Original job description

ARS Pharmaceuticals is a fast-growing, innovative company dedicated to transforming the treatment of severe allergic reactions with neffy®, the first and only FDA-approved needle-free epinephrine product. If you’re motivated to make a meaningful impact, this is your opportunity to join a collaborative, entrepreneurial, and inclusive culture.

THE OPPORTUNITY

The Manager / Sr. Manager, Technical Operations will play a key role in executing Technical Operations programs that support the continued development and commercial supply of neffy™. The successful candidate will combine strong technical judgment, project management, and external partner leadership in a highly collaborative environment.

Working closely with internal stakeholders and CMOs, this role provides technical and operational leadership across the ARS outsourced manufacturing network. Responsibilities include leading Technical Operations projects, supporting formulation and process development, technology transfer, GMP manufacturing activities, and resolution of technical and operational issues. The position ensures project scope, timelines, deliverables, responsibilities, and budgets remain aligned while proactively identifying and escalating risks to support compliant, reliable, and on-time product supply.

ESSENTIAL DUTIES & RESPONSIBILITIES:

Manage cross-functional Technical Operations projects and day-to-day technical and operational interactions with assigned external partners, including scope, timelines, deliverables, responsibilities, budgets, risks, key milestones, project meetings, action tracking, scopes of work, proposals, change orders, and CMO/vendor performance metrics and KPIs (e.g., service, quality, delivery, capacity, and right-first-time).
Serve as a Technical Operations point of contact for assigned external manufacturing partners and work closely with CMOs and internal stakeholders to ensure execution against agreed project plans and supply requirements.
Provide technical oversight of formulation and process development, scale-up, technology transfer, process characterization, process validation/PPQ, and continued process verification activities, as applicable.
Plan and support clinical and commercial manufacturing campaigns in coordination with CMOs, Supply Chain, Quality Assurance, and other internal functions; provide on-site/person-in-plant support for key manufacturing activities as needed.
Review manufacturing and process documentation, including master and executed batch records, protocols, reports, process performance data, vendor change controls, investigations, and annual/product reviews, for technical accuracy and process performance.
Lead or support technical assessment and resolution of manufacturing deviations, out-of-specification or atypical results, and other process issues; contribute to root-cause analysis and appropriate corrective and preventive actions in partnership with Quality Assurance.
Assess proposed manufacturing and process changes for technical impact and support cross-functional evaluation of quality, supply, and regulatory implications.
Monitor and trend manufacturing and process performance data to identify emerging risks, process drift, and opportunities for continuous improvement and operational excellence.
Support vendor selection, onboarding, and qualification activities in collaboration with Quality Assurance, Supply Chain, Procurement, and other stakeholders.
Communicate project status, technical risks, manufacturing issues, and recommend actions clearly to Technical Operations leadership and cross-functional stakeholders; escalate significant issues to appropriate decision-makers.
Support preparation and review of CMC information for regulatory submissions and responses to health authority questions, as required.
Support Technical Operations process improvement, business continuity, capacity planning, and other strategic operational initiatives as assigned.
Support commercial supply operations managed within Technical Operations, including coordination with third-party logistics (3PL) providers, distribution partners, and external manufacturing/packaging partners to maintain reliable product supply.
Support product serialization activities, including EPCIS data exchange and operational compliance with applicable Drug Supply Chain Security Act (DSCSA) requirements, working with packaging, distribution, Quality Assurance, and other partners as appropriate.
Support clinical supply activities, including coordination with Clinical Operations and external vendors for clinical packaging, labeling, distribution, inventory/expiry management, and Interactive Response Technology/Interactive Web Response System (IRT/IWRS) activities, as applicable.

KNOWLEDGE, SKILLS, AND ABILITIES:

Strong working knowledge of current Good Manufacturing Practices (cGMP), pharmaceutical manufacturing operations, and applicable quality systems and regulatory expectations.
Demonstrated technical understanding of formulation, manufacturing processes, scale-up, technology transfer, process validation, and process performance sufficient to critically evaluate CMO data and recommendations, work effectively in cross-functional technical teams, and hold external partners accountable to commitments.
Strong project and vendor management skills, with demonstrated ability to manage multiple priorities, timelines, deliverables, and external partners in a fast-paced environment.
Strong analytical and problem-solving skills, including the ability to evaluate complex manufacturing or process issues, develop recommendations, and communicate the rationale for action.
Excellent written, verbal, and presentation skills with the ability to communicate effectively across functions and organizational levels, including senior management and external partners.
Well-organized, detail-oriented, and able to identify and escalate risks while maintaining focus on execution and business priorities.
Proficiency with Microsoft Office and project/reporting tools; experience with project management, continuous improvement, or operational excellence methodologies is a plus.
Working knowledge of commercial and clinical supply operations relevant to Technical Operations, including 3PL interfaces, serialization/EPCIS and DSCSA requirements, and clinical IRT/IWRS processes; direct experience in one or more of these areas is preferred.
Must be able to travel domestically and internationally up to approximately 20% to support external manufacturing partners and key project activities.

EDUCATION AND EXPERIENCE:

Bachelor’s degree in pharmaceutical sciences, chemistry, chemical engineering, engineering, or a related scientific/technical discipline; an advanced degree is a plus. An acceptable combination of education and relevant experience will also be considered.
Minimum of 5 years of relevant pharmaceutical/biotechnology experience in Technical Operations, manufacturing, process/formulation development, CMC, supply chain, or a related function.
Experience working with external CMOs/CDMOs and supporting GMP clinical and/or commercial manufacturing is strongly preferred.
Experience with drug-device combination products, nasal/inhalation products, sterile manufacturing, commercial product launch, or PPQ is preferred.
Experience reviewing manufacturing batch records and process documentation and supporting technical investigations, change controls, and regulatory CMC activities is preferred.
Experience supporting commercial distribution/3PL operations, serialization/EPCIS and DSCSA compliance, and/or clinical supply and IRT/IWRS activities is preferred.

At ARS, we are proud to offer a highly competitive compensation & benefits package.

The full-time salary range for this posted position is $140,000 to $175,000 and may be eligible for a discretionary annual performance bonus. Actual pay rates are determined by considering multiple factors including qualifications, relevance of experience, education & credentials, subject matter expertise, and other job-related factors permitted by law.

This position is also eligible for Equity, 401k matching, and our excellent benefits package including 100% employer paid Medical, Dental & Vision for employees. View the full package here: ARS Careers Page

ARS Pharmaceuticals believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. ARS Pharmaceuticals is also committed to providing reasonable accommodation to qualified individuals so that an individual can perform their job-related duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at careers@ars-pharma.com

The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.

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