Jobs in the United States

25+ jobs

Save this search

Added just now
Associate Director, Paid Search
Dentsu International Americas, LLC
NY
dentsu is looking for a Associate Director, Paid Search to join our team. You will act as one of the senior leaders of our client’s Paid Search programs.
Added just now
Relationship Banker / Senior Relationship Banker - Butler Road
Truist Bank
Mauldin, SC
Responsible for providing an industry leading client service experience both in person and on the phone through the development and expansion of new and existing client relationships.…
Added just now
Relationship Banker/Senior Relationship Banker - Daniel Village
Truist Bank
Augusta, GA
Responsible for providing an industry leading client service experience both in person and on the phone through the development and expansion of new and existing client relationships.…
Added just now
CPI Investigation Worker Trainee
TX-HHSC-DSHS-DFPS
VERNON, TX
Added just now
RN Assistant Director of Nursing Intensive Care Unit (ICU)
MedStar Health
Clinton, MD
…a timely manner. Ensures the reviews reflect the individual associate's ability to meet performance expectations and beneficial ongoing developmental goals. Provides associates with ongoing…
Added just now
Process Engineer II/III - API (Recovery) Mon-Fri shift
Novo Nordisk
Clayton, NC
Support the ongoing development of the department processes. Support daily operations as well as continuous improvement of department processes including ensuring system & equipment…
Added just now
Senior Associate - Sample Operations Support
Novo Nordisk
Plainsboro, NJ
…benefit of our stakeholders. We focus on personal performance and development and have a culture centered on helping leaders create the conditions for people to be at their best. If you…
Added 1 min ago
US-Broussard-Field Prof-Reserv Eval, Prin-212822
Halliburton
Broussard, LA
…Maintains job schedules, helps perform PPRs and manages the career development of the Associate Field Professionals (AFPs), Field Professionals (FPs), and Senior Field Professionals (SFPs)…
Added 1 min ago
Showroom Manager
Ferguson Enterprises, LLC
San Antonio, TX
Actively leads day-to-day showroom operations which includes the Showroom team, collaboration with Senior Showroom Manager, Showroom Operations Manager to focus on Showroom Displays, the…
Added 1 min ago
WO
Associate
Woods Oviatt Gilman LLP
Rochester, NY
- $120,000 to $170,000 USD / year
We are seeking a Real Estate Associate Attorney with 2 to 5 years of experience handling complex commercial real estate transactions. This is a substantive role with meaningful deal…
Added 1 min ago
Senior Service Associate Mon-Fri. 9am-530pm HLD ADC
FTZ Fritz
United States
Utilize computer-based warehouse management system (WMS) to perform all warehouse activities including outbound process, inbound process and inventory control
Added 2 mins ago
Center Manager for Plasma Donation Center
GRIFOLS, S.A.
AR-Conway, CA
Monitor and evaluate operations. Develop action plans to maximize center efficiency and supervise the implementation of process improvements.
Added 3 mins ago
Senior Employee Relations Manager
Clayton
The Senior Employee Relations Manager role ensures consistent and thorough management of Employee Relations processes, including performance management. Leverages advanced business and…
Added 3 mins ago
Senior Associate - Sample Operations Support
Plainsboro
…benefit of our stakeholders. We focus on personal performance and development and have a culture centered on helping leaders create the conditions for people to be at their best. If you…
Added 3 mins ago
Process Engineer II/III - API (Recovery) Mon-Fri shift
Clayton
Support the ongoing development of the department processes. Support daily operations as well as continuous improvement of department processes including ensuring system & equipment…
Added 3 mins ago
GI
Senior Software Engineer, Compute Platform
GitHub, Inc.
United States
- $127,800 to $339,000 USD / year
GitHub is the world’s leading platform for agentic software development - powered by Copilot to build, scale, and deliver secure software. Over 180 million developers, including more than…
Added 4 mins ago
GD
Practice Manager, Investment Funds
Gibson Dunn
Washington, DC
- $230,000 to $280,000 USD / year
Talent Planning: Support talent planning by acting as a liaison with Human Resources, Professional Development, and Recruiting, including regular assessment of recruiting and senior talent…
Added 4 mins ago
FSP Sr Clinical Research Associate
PPD Development, LP
Remote, United States
Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages…
Added 4 mins ago
FSP Sr CRA I
PPD Development, LP
Remote, United States
As a Senior Clinical Research Associate I in our FSP model, you will be dedicated to one specific client, acting as a representative of the client while exercising strong communication and…
Added 5 mins ago
Senior Structural Associate
Thornton Tomasetti
Kansas City, MO
As a Senior Associate in our Structural Practice, you’ll step into a role where your expertise drives project direction, client strategy, and technical excellence. You’ll serve as a trusted…
Added 5 mins ago
Associate Director of Business Process & Operations
Netradyne
San Francisco, CA
The Associate Director of Business Process & Operations leads enterprise-wide business process transformation and operational excellence across multiple value streams (Go-To-Market,…
Added 5 mins ago
WF
Senior Associate, Institutional Professional Services Representative
Webull Financial
Saint Petersburg, FL
- $90,000 to $115,000 USD / year
Experience in team leadership, process design, and KPI development.
Added 6 mins ago
CS
Field Service Engineer (Orlando, Melbourne, Jupiter FL)
CareFusion Solutions, LLC
FL
- $28.2 to $45.1 USD / hour
…availability and reduce inefficiencies in the medication use process. At almost every point in the medication use process, safety and efficiency can be increased with the comprehensive…
Added 6 mins ago
Senior Specialist, Medical Affairs
Becton, Dickinson and Company
United States
Support process improvement and standardization of Medical Affairs planning, tracking, documentation, and execution practices.
Added 7 mins ago
3K
Engineer – GMP Drug Product Manufacturing Equipment & Reliability - (JP16085)
3 Key Consulting
Thousand Oaks, CA
- $41 to $46 USD / hour
Provide system ownership for Biopharmaceutical process equipment. Identify, support, and/or lead implementation of engineering based improvements or upgrades to the equipment or facility…

Cosette Pharmaceuticals Inc.

Associate Director, Technical Services

Bridgewater, United States

Apply About employer

Applications open in a new tab.

Job details

Education: Bachelor’s degree
Posting language: English
Posted: Nov 4, 2026

Original job description

Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product development, manufacturing, and commercial operations. Cosette has a fast-growing portfolio of branded pharmaceuticals consisting of products in the cardiology, women's health, and migraine markets. Cosette has a long history in quality manufacturing of complex dosage forms including topical creams, ointments, oral liquids/solutions and suppositories, which has led to consistent supply to customers and commercialization success. Cosette has corporate and manufacturing facilities in New Jersey and North Carolina and is supported by more than 300 dedicated employees across all functional areas. Innovating every day.™ Reporting directly to the Vice President Technical Services and 3rd Party Operation, the Associate Director, Technical Services provides scientific and technical leadership for Cosette's commercial product portfolio and external manufacturing network. The role leads technology transfer, lifecycle management, manufacturing and packaging process changes, technical investigations, validation strategy, process optimization, and ongoing technical support for products manufactured through third-party CMOs/CPOs. The Associate Director serves as the primary Technical Services leader within Scientific Affairs and partners closely with Analytical, Regulatory Affairs, Quality, Operations, Supply Chain, Alliance Management, Strategic Sourcing, and external manufacturing partners. The Associate Director is expected to ensure that technical decisions affecting commercial products are scientifically sound, appropriately documented, compliant with regulatory expectations, and implemented effectively while supporting reliable product supply and business objectives. Technical Services is accountable for scientific and technical leadership supporting commercial products, while Operations retains accountability for manufacturing execution and supply continuity. The Associate Director is expected to work in close partnership with supply chain so that technical strategy and manufacturing execution remain fully aligned.

KEY RESPONSIBILITIES

Technology Transfer Leadership Lead end-to-end technology transfer activities for acquired products, new or alternate manufacturing sites, packaging sites, and other product transfers. Establish transfer strategies, technical requirements, risk assessments, validation approaches, acceptance criteria, project milestones, and readiness expectations. Coordinate formulation/process knowledge, equipment capability, raw materials, packaging components, validation, stability, regulatory requirements, and manufacturing readiness. Proactively identify technical risks, dependencies, and decisions requiring escalation and ensure transfers progress according to approved timelines. Provide ongoing scientific and technical leadership for Cosette's commercial portfolio and serve as a primary escalation point for complex manufacturing, packaging, and product-performance issues. Partner with Operations and external manufacturing organizations to determine root causes, develop technically appropriate solutions, and implement sustainable corrective and preventive actions. Product Lifecycle Management Lead the technical assessment and implementation of lifecycle changes affecting approved products, including API and raw-material changes, specifications, manufacturing and packaging processes, components, equipment, manufacturing site transfers, shelf-life extensions, process improvements, and cost-improvement initiatives. Ensure changes are supported by appropriate scientific rationale, risk assessment, comparability strategy, validation, stability, and regulatory evaluation. Technical Investigations, Deviations & CAPA Provide technical leadership for scientifically complex deviations, investigations, OOS/OOT events, manufacturing failures, recurring process issues, and product complaints requiring technical assessment. Work closely with Quality while maintaining clear distinction between Quality System ownership and scientific/technical assessment ownership. Ensure investigations are scientifically rigorous, identify credible root causes, and result in effective and sustainable CAPAs. CMO/CPO Technical Oversight Serve as a senior technical interface with Cosette's CMO/CPO network. Establish effective technical governance with external manufacturing partners and ensure timely review of manufacturing performance, technical investigations, process changes, validation documentation, stability information, technical change controls, and manufacturing/packaging documentation. Provide technical leadership for process validation, packaging validation, hold-time studies, cleaning-validation technical assessments, and continued process verification, as applicable. Ensure validation strategies are scientifically justified, risk-based, compliant, and appropriate for the product and manufacturing process. API, Supplier & CMO/CPO Selection Serve as a core member of cross-functional teams evaluating new or alternate API manufacturers, CMOs, CPOs, critical component suppliers, and manufacturing technologies. Lead or coordinate the technical assessment of manufacturing capability, process compatibility, technical risk, transfer requirements, and scalability. Technical Risk Management Proactively identify and mitigate risks involving manufacturing robustness, single-source materials, API, components, equipment, process capability, CMO capabilities, technology transfers, and product lifecycle. Develop mitigation and contingency strategies with cross-functional partners and escalate material risks in a timely manner. Regulatory & Quality Partnership Work closely with Regulatory Affairs to ensure technical changes are appropriately assessed for regulatory impact and that technical documentation supports supplements, annual reports, Health Authority responses, and other submissions. Partner with Quality to ensure cGMP compliance and robust quality-system execution while preserving clear accountability for scientific assessment and independent Quality oversight. Supply Continuity Support Partner closely with Operations and Supply Chain to provide technical support for supply continuity. Operations remains accountable for manufacturing execution and supply continuity, while Technical Services proactively identifies, assesses, and resolves technical risks that could affect manufacturing reliability, release readiness, or product availability. Portfolio, Budget & Resource Management Maintain an integrated Technical Services portfolio covering active technology transfers, lifecycle projects, technical investigations, validation activities, CMO technical initiatives, product risks, regulatory commitments, and critical milestones. Establish clear priorities, owners, timelines, risks, and resource requirements in partnership with PMO. Develop and manage the annual Technical Services budget and forecasts, provide visibility to spend by product/project/CMO, identify budget risks early, and recommend mitigation or reprioritization as needed. Business Development, Due Diligence & Integration Support technical due diligence for potential product and company acquisitions by evaluating manufacturing processes, technical risks, CMOs/CPOs, API sources, validation status, lifecycle requirements, capital needs, and technology-transfer complexity. Following acquisition, lead or support technical integration and transfer activities to ensure effective transition into Cosette's operating model.

PROFESSIONAL EXPERIENCE / QUALIFICATIONS

Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Pharmacy, or a related scientific/engineering discipline required; Master's degree, PharmD, or PhD preferred.
Approximately 12+ years of progressive pharmaceutical industry experience, including substantial experience supporting commercial manufacturing, technology transfer, process validation, lifecycle management, and external manufacturing.
Demonstrated experience working with CMOs/CDMOs/CPOs and leading complex technical programs across multiple products and manufacturing sites.
Experience with branded and/or complex pharmaceutical products and post-approval lifecycle management strongly preferred.
Strong knowledge of pharmaceutical manufacturing, scale-up, process validation, cGMP, investigations, change control, CAPA, stability, CMC, analytical methods, manufacturing/packaging processes, and FDA regulatory expectations.

JOB-SPECIFIC COMPETENCIES

Strategic and scientific thinking with the ability to connect technical decisions to patient, supply, quality, regulatory, cost, and commercial outcomes.
Strong business acumen and ability to balance technical risk, compliance, cost, timing, and supply priorities.
Timely, data-driven decision making and effective technical risk management.
Cross-functional leadership and influence across Scientific Affairs, Operations, Quality, Supply Chain, Regulatory, Alliance Management, and external partners.
Executive-level communication of complex technical risks, recommendations, and decisions.
People leadership, coaching, succession planning, and development of technical talent.
High ownership, accountability, transparency, and solution-oriented problem solving.

Benefits

Hired applicants will be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, health saving account, employee assistance program, tuition reimbursement program, parental leave, wellness program, paid time off, volunteer time, and holidays. Physical Requirements This role will follow a hybrid work schedule, requiring three (3) onsite days per week at our Bridgewater, NJ office.

Apply About employer

More about this job

Skills

Technical support
Regulatory affairs
Supply chain management
Packaging
Hazard assessment
Chemical engineering
Pharmaceutical industry
Pharmaceutical products
Pharmaceutical processes
Packaging processes
Regulatory compliance
Decision making
Risk management
Leadership
Communication skills
Coaching
Problem solving

Report this job