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Associate Director Nanoparticle Formulation Jobs

Actox

The Associate Director, Clinical Pharmacology Lead (AD, CPhL) is the entry level Clinical ... drug interaction, formulation development, dose selection decision, impact of renal/hepatic ...

Ardena

Associate Director, Finance

Somerset, NJ · On-site

Ardena provides integrated services spanning drug substance development, drug product formulation ... Ardena is hiring an Associate Director, Finance to join the Finance team at our Somerset, NJ site.

Loxo CS Demo

Associate Dir of Sales

Denver, CO · On-site

ASSOCIATE SALES DIRECTOR REPORTING TO: SALES & MARKETING LEADER, CPI COMPANY: Bigtime PHARMA ... From development and contract manufacturing to formulation and supply chain management, Corden ...

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Associate Director Nanoparticle Formulation information

What does an associate director nanoparticle formulation do?

An Associate Director of Nanoparticle Formulation oversees the development and optimization of nanoparticle-based drug delivery systems and formulations. They lead teams in designing, testing, and scaling up nanoparticle products for pharmaceutical or biotech applications. This role also involves collaborating with other departments, ensuring regulatory compliance, and guiding research strategies to meet organizational objectives. Additionally, they mentor junior scientists and contribute to the scientific direction of projects.

What are the key skills and qualifications needed to thrive as an associate director nanoparticle formulation?

To excel as an Associate Director of Nanoparticle Formulation, you generally need an advanced degree (Ph.D. or MSc) in chemistry, pharmaceutical sciences, or a related field, along with experience in drug delivery and formulation development. Proficiency with analytical characterization tools (such as DLS, TEM, HPLC), formulation equipment, and regulatory documentation systems is typically required. Strong leadership, project management, and cross-functional communication skills help drive innovation and lead teams effectively. These competencies ensure the development of safe, effective nanoparticle drug products and the successful execution of complex R&D projects.

What are some common challenges faced by an associate director nanoparticle formulation, and how can they be addressed?

Associate Directors in Nanoparticle Formulation often encounter challenges such as scaling up laboratory formulations for commercial production, ensuring batch-to-batch consistency, and meeting stringent regulatory requirements. Addressing these challenges involves close collaboration with cross-functional teams, such as analytical development, process engineering, and quality assurance. Successful leaders in this role proactively implement robust process controls, maintain open communication with team members, and stay updated on regulatory trends to anticipate and resolve issues effectively.

What are popular job titles related to Associate Director Nanoparticle Formulation jobs?

For Associate Director Nanoparticle Formulation jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Nanoparticle Formulation job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Supervisor, Formulation (2nd Shift)

Grand Island, NY • On-site

Fresenius Kabi
Pharmaceutical and Medicine Manufacturing
Learn more about Fresenius Kabiexternal

$73K - $103K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Fresenius Kabi rating

8.3

Company rating: 8.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

Job Summary
Responsible for the overall supervision, direction, and coordination of the Grand Island formulation suites and the surrounding controlled environmental area associated with the formulation of liquid parenterals. Ensures adequate systems, equipment and resources are in place to meet production schedules, and that products are manufactured to specification and in complete accordance with applicable SOP's, DEA, OSHA and cGMP's regulations. This position directly supervises 12 to 15 direct reports accountable for formulating liquid products against delivered production schedules and compliance regulations. Staff development, hiring, disciplinary processes, and direction to complete assigned activities are required.
The formulation supervisor ensures the safe and quality focused work environment while accepting accountability for all activities within this position's control. Investigation work, corrective, preventative, and practice versus procedure auditing as needed.
Salary Range: $73,614-$103,000 + 6% annual bonus
Hours: M-F; 2PM-10:30PM
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Responsibilities
  • Ensures adequate systems are in place to effectively manufacture Bulk product, and clean/store/prepare equipment and compounds.
  • Ensures all area SOPs are reviewed/revised to encompass any changes in procedure and/or two-year review.
  • Ensures adequate resources are available to clean and prepare equipment.
  • Ensures all area personnel are current in their training requirements; Trains employees to area-specific Curricula and company policies and procedures.
  • Ensures a safe work environment and that all personnel work in a safe manner.
  • Ensures corrective actions for investigations and audit observations are completed in a timely manner. Ensures all documentation is correct and addresses errors effectively and expeditiously. Completes Batch Record review for area in the designated time expectations.
  • Works closely with HR on policy changes, interpretation and execution, hiring of new employees, employee disciplinary action, performance appraisals and performance management.
  • Works with Technical Services/Maintenance to reduce downtime and improve equipment reliability; Assists with design of new systems/facilities related to the department.
  • Works closely with Material Management and Quality regarding component problems and inventory maintenance. In addition to each complexes inventory management and movement via SAP modules.
  • Works closely with Environmental, Maintenance, Metrology, and Validation to ensure area environmental monitoring, PM, calibration, and re-qualification schedules are met

Requirements
  • High School diploma or GED. BS/BA in Science related discipline or equivalent relevant work experience is preferred.
  • 4-5 years of pharmaceutical experience in compounding preferred.
  • Working knowledge of SOP's and cGMP's rules and regulations.
  • Proficiency in Microsoft Office required
  • Must be able to work with Antineoplastic products and assist in the Nanotechnology department.
  • Heavy lifting is required. (Ability to regularly lift 25 lbs and occasionally lift 50 lbs without strain.)

Additional Information
We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.
Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at-will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.
Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

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