Aquestive Therapeutics, Inc.

Product Development Program Manager

Aquestive Therapeutics, Inc.$110K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific, engineering, healthcare, or business discipline; advanced degree preferred.
  • 7+ years of experience in pharmaceutical, biotechnology, or life sciences development; proven project management track record.
  • Ability to establish productive relationships with stakeholders, partners, and vendors.
  • Strong leadership and cross-functional management skills are essential.
  • Experience managing integrated timelines, critical paths, and resource allocations with a focus on governance deliverables.
  • Solid understanding of the pharmaceutical development lifecycle and cross-department dependencies.
  • Excellent communication skills, both verbal and written.

Responsibilities

  • Leads multiple product development projects to success.
  • Develops and manages a comprehensive development plan for each product, including timelines and risk assessments.
  • Integrates functional development plans into a unified cross-functional strategy with clear responsibilities.
  • Identifies, communicates, and mitigates project risks throughout the project lifecycle.
  • Maintains tracking of program risks and escalates issues to management as necessary.
  • Ensures adherence to the product development process using thorough documentation and milestone reviews.
  • Communicates effectively across departments to align on product development objectives.

Benefits

  • Comprehensive health insurance packages.
  • Flexible working arrangements to support work-life balance.
  • Opportunities for professional development and career growth.
  • Collaborative and inclusive company culture.
  • Employee wellness programs promoting a drug-free workplace.
Full Job Description
Job Summary:

Responsible for leading and project managing the progress of an assigned portfolio of product development projects (typically 2-3 at any one time). Accountable for developing and executing integrated cross-functional development plans and driving alignment across Clinical, Regulatory, CMC, Manufacturing, Quality, Commercial, and Finance functions. Accountable for the efficient and effective use of company resources towards the successful completion of product development milestones. Requires leadership, tenacity, critical thinking and the ability to build internal and external alliances. Also requires a balance of leadership capabilities, organizational skills, and a hands-on approach to program leadership and execution.

Responsibilities:

  • Leads the company to success on an assigned portfolio of product development projects.
  • Develops and owns a comprehensive product development plan (including timelines, resource requirements, budget, risks, dependencies, and key milestones) in conjunction with executive management for each assigned product.
  • Integrates functional plans into a single cross-functional development plan with clear ownership, dependencies, and accountabilities for key deliverables.
  • Identifies project risks and formally measures, communicates and manages the risks and associated mitigation strategies.
  • Maintains program-level risk, issue, decision, and dependency tracking and escalates matters requiring management intervention.
  • Leads the Aquestive Product Development Process (PDP) for all assigned projects ensuring use of checklists, documentation, and appropriate stage gate/milestone reviews are conducted.
  • Works on a cross-functional basis to ensure company alignment behind product development timelines and goals (internal development activities, clinical requirements, regulatory requirements, engineering & manufacturing requirements, and commercial & marketing requirements).
  • Leads through influence in a matrixed environment while respecting the decision authority and accountability of functional leaders.
  • Acts as Aquestive's lead representative on external pipeline projects; ensures external pipeline projects are properly managed, resourced, and progressed.
  • Facilitates active communication and timely decision making regarding projects.
  • Prepares and presents concise program updates, risks, mitigation plans, and key decisions to senior leadership and applicable governance teams.
  • Works with Commercial, Finance, and the Executive Leadership Team to continually assess the return on investment (ROI) for each product.
  • Maintains core program management deliverables, including integrated timelines, resource plans, budgets, governance materials, milestone forecasts, decision records, project data, and executive reporting.
  • Works as an integral member of the Product Development team to improve the product development process within Aquestive.
  • Navigates the internal Aquestive environment effectively, maintaining flexibility while driving achievement of program goals and timelines.


Qualifications:

  • Bachelor's degree in a scientific, engineering, healthcare, or business discipline; advanced degree preferred.
  • 7+ years of experience leading pharmaceutical, biotechnology, or life sciences development programs or projects; the successful candidate must be able to provide a proven track record of project management results.
  • Demonstrated ability to build productive relationships with internal stakeholders, external partners, and vendors.
  • Strong leadership and cross-functional management skills.
  • Demonstrated experience managing integrated timelines, critical paths, resources, budgets, risks, dependencies, milestones, and governance deliverables.
  • Working knowledge of the pharmaceutical development lifecycle and the interdependencies among Clinical, Regulatory, CMC, Manufacturing, Quality, and Commercial functions.
  • Ability to balance and prioritize a demanding workload and multiple projects/tasks in a fast-paced environment.
  • Ability to drive and manage project strategy while focusing on tactical deliverables.
  • Strong analytical and problem-solving skills.
  • Excellent verbal and written communication skills.
  • Strong collaborative mindset and ability to lead through influence without direct authority.
  • Experience presenting program status, risks, options, and recommendations to senior leadership preferred.
  • Experience with project or portfolio management tools required; PMP or comparable program management certification preferred but not required.


The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.

As part of Aquestive's employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place.

The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education. Expected salary range: $110,000.00 to $130,000.00/year

About Aquestive Therapeutics, Inc.

Aquestive Therapeutics, Inc. is a specialty pharmaceutical company. The Company is focused on identifying, developing and commercializing differentiated products to address unmet medical needs. Its product candidates include AQST-108, AQST-305, AQST-109, AQST-119, and AQST-120. Its AQST-108 is designed to provide quick relief of symptoms associated with an acute migraine. AQST-305 is designed to provide relief of symptoms associated with Parkinson's disease and other indications. AQST-109 is designed to deliver epinephrine via an oral cavity film to treat anaphylaxis. AQST-119 is designed to deliver tadalafil via an oral cavity film for the treatment of erectile dysfunction. AQST-120 is designed to deliver octreotide via an oral cavity film for the treatment of acromegaly and neuroendocrine tumors. The Company's products are developed using its PharmFilm technology.
Learn more about Aquestive Therapeutics, Inc.
Size
157 employees
Market Cap
$45.9 million
Industry
Net Income
-$55.7 million
Founded
2000
5 Year Trend
-0.4%
Revenue
$45.8 million
NASDAQ

Similar Jobs

More Jobs at Aquestive Therapeutics, Inc.

More Pharmaceuticals & Biotech Jobs

Find similar Product Development Program Manager jobs: