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Aquestive Therapeutics

Process Engineer

Portage, IN

Responsible for leading product technology transfer and process scale-up for new and existing thin film and dispensed LCO (Lotion, Cream, Ointment) pharmaceutical products at Aquestive Therapeutics ...

Aquestive Therapeutics

Process Engineer

Portage, IN · On-site

Responsible for leading product technology transfer and process scale-up for new and existing thin film and dispensed LCO (Lotion, Cream, Ointment) pharmaceutical products at Aquestive Therapeutics ...

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What is an Aquestive?

Aquestive is not a traditional job title but rather the name of a pharmaceutical company specializing in developing and commercializing medicines using drug delivery technology, particularly oral film formulations. Employees at Aquestive work in various roles including research and development, regulatory affairs, manufacturing, and sales to bring innovative therapies to patients. The company is known for its work on products that improve drug administration and patient compliance, especially for those who have difficulty swallowing pills.

What are the key skills and qualifications needed to thrive as an employee at Aquestive Therapeutics?

To thrive at Aquestive Therapeutics, you typically need a background in pharmaceutical sciences, chemistry, or a related field, often supported by relevant degrees or industry experience. Familiarity with drug delivery technologies, regulatory compliance systems, and laboratory information management systems (LIMS) is commonly required. Strong analytical thinking, teamwork, and effective communication skills help individuals excel in cross-functional environments. These competencies are important for driving innovation, ensuring quality, and supporting the company's mission to develop advanced therapeutic solutions.

What collaborative opportunities can professionals expect when working at Aquestive in a scientific or technical role?

At Aquestive, scientific and technical professionals often work in cross-functional teams that include colleagues from research and development, manufacturing, regulatory, and quality assurance. This collaborative environment allows for comprehensive problem-solving and innovation, especially in the development and commercialization of pharmaceutical products. Regular meetings and project updates foster open communication, and team members are encouraged to share insights and feedback. This structure not only enriches the work experience but also provides valuable exposure to diverse aspects of the drug development process.
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Infographic showing various Aquestive job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Manufacturing Associate Packaging (3rd shift, 12:00a to 8:30a)

Aquestive Therapeutics

Portage, IN • On-site

$13.75 - $17/hr

Full-time

Re-posted yesterday

Job description

Summary:
Follows the lead of the Packaging Specialists during the packaging of a batch and during the closing of a batch. Inspects the finished product before placing the finished product into a carton. Checks the quality of the finished product by performing in process checks and documenting findings in batch record. Notifies Quality and Production Supervisors if the product fails the required specifications.
Responsibilities:
• Maintains a cGMP area.
• Follows all required SOPs and work instructions and safety procedures.
• Documents all required information to ensure compliance.
• Performs in-process checks efficiently.
• Supports packaging operators during the opening and closing of a batch.
• Places finished product into cartons and seals.
• Supports daily and weekly cleans.
• Follows all DEA requirements to ensure compliance to regulations.
• Other projects and duties as assigned.
Qualifications:
• High School Diploma or GED required; college degree desired for future opportunities within Aquestive.
• Possess basic mathematical skills: addition, subtraction, multiplication, and division.
• Ability to communicate effectively both orally and written.
• Desire to work in fast paced, heavily regulated environment that requires significant attention to detail; high degree of accuracy and utmost integrity to ensure the safety and efficacy of our products.
• Willingness to work various shifts in a 24/7 operation.
• Strong attention to detail to ensure effective inspection.
Willingness to be proactive; comfortable in raising concerns regarding inspection results.
• Ability to take specific direction, with no room for error.
• Ability to work in a team environment, and collaborate effectively across teams, functions, and shifts.
• Ability to lift up to 50 pounds.
The above statements are intended to describe the general nature and level of the work being performed by employees assigned to this position. This is not intended as 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.
Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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