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Full Time Distillery Chemist Jobs (NOW HIRING)

API Manufacturing Technician

Groton, CT · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Distillation, extraction, and phase separation * Crystallization, filtration, and drying ... Collaborate with Quality, Compliance, Process Chemistry, Tech Transfer, and Production teams.

Lab Technician

Ashland, MO · On-site

$25 - $26/hr

Support refinement processes such as winterization, filtration, distillation, and solvent recovery ... Background in chemistry, biology, or related field (formal education or hands-on experience)

New

Work with production planner on raw materials or distillation needed for stocked products and or ... This is a full-time position, Monday through Friday. Travel * This position requires less than 10% ...

Showing results 21-31

Full Time Distillery Chemist information

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$17

$30

$52

How much do full time distillery chemist jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for full time distillery chemist in the United States is $30.99, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $35.58 per hour, depending on experience, location, and employer.

What is a full time distillery chemist?

Full Time Distillery Chemists are professionals who work in distilleries to ensure the quality, safety, and consistency of alcoholic beverages through chemical analysis and testing. They monitor the production process, analyze ingredients and final products, and help optimize recipes and procedures for better efficiency and taste. These chemists also ensure compliance with regulatory standards and may assist in research and development of new products. Their expertise is crucial for maintaining product quality and safety in the distillation industry.

What are some common challenges a full time distillery chemist may face when ensuring product consistency across different batches?

A Full Time Distillery Chemist often encounters the challenge of maintaining product consistency due to natural variations in raw materials, changes in environmental conditions, and differences in equipment performance. To address these issues, chemists must carefully monitor fermentation, distillation, and aging processes, often performing regular analytical tests and adjusting parameters as needed. Collaboration with production and quality assurance teams is crucial to swiftly resolve any discrepancies and uphold the brand's quality standards. Staying current with industry best practices and technological advancements also helps mitigate inconsistencies and ensures continuous improvement.

What is the difference between Full Time Distillery Chemist vs Full Time Quality Control Chemist?

AspectFull Time Distillery ChemistFull Time Quality Control Chemist
CredentialsBachelor's degree in Chemistry, Biochemistry, or related fieldBachelor's degree in Chemistry, Biochemistry, or related field
Work EnvironmentDistilleries, laboratories focused on fermentation and distillation processesQuality labs, manufacturing facilities, testing laboratories
Industry UsagePrimarily in spirits, whiskey, and alcohol production

The main difference between a Full Time Distillery Chemist and a Full Time Quality Control Chemist lies in their focus areas. The distillery chemist specializes in the fermentation and distillation processes specific to spirits production, while the quality control chemist concentrates on testing and ensuring product quality across various stages. Both roles require similar educational backgrounds and work environments but serve different functions within the beverage manufacturing industry.

What are the key skills and qualifications needed to thrive as a full time distillery chemist?

To thrive as a Full Time Distillery Chemist, you need a solid background in chemistry or chemical engineering, typically supported by a relevant degree and laboratory experience. Familiarity with analytical instrumentation such as gas chromatography (GC), high-performance liquid chromatography (HPLC), and quality control systems is essential. Attention to detail, problem-solving, and strong communication skills help ensure product consistency and regulatory compliance. These skills are crucial for maintaining product quality, ensuring safety standards, and supporting efficient production in a distillery environment.
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What are the most commonly searched types of Distillery Chemist jobs?

The most popular types of Distillery Chemist jobs are:

What states have the most Full Time Distillery Chemist jobs?

States with the most job openings for Full Time Distillery Chemist jobs include:

Infographic showing various Full Time Distillery Chemist job openings in the United States as of August 2026, with employment types broken down into 81% Full Time, 12% Part Time, 1% Temporary, 5% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories


Job description

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Job Description

Join a multi-disciplinary team supporting the cGMP production of clinical-scale Active Pharmaceutical Ingredients (APIs). In this hands-on manufacturing role, you'll support API development through equipment operation, batch execution, documentation, and continuous improvement activities.

Typical process operations include:

  • Charging solids and liquids to vessels
  • Distillation, extraction, and phase separation
  • Crystallization, filtration, and drying
  • Equipment cleaning and preparation

Key Responsibilities

  • Execute process instructions and batch records in a cGMP environment.
  • Prepare, operate, monitor, sample, and clean pharmaceutical manufacturing equipment.
  • Support equipment commissioning, qualification, and troubleshooting activities.
  • Complete manufacturing documentation, including batch records, cleaning records, and in-process sampling documentation.
  • Follow cGMP, safety, environmental, and site procedures at all times.
  • Report deviations, safety concerns, and quality observations promptly.
  • Manage manufacturing waste according to approved procedures.
  • Participate in shift handovers and maintain clear communication across teams.
  • Collaborate with Quality, Compliance, Process Chemistry, Tech Transfer, and Production teams.
  • Support SOP reviews and continuous improvement initiatives.
  • Manage priorities independently and assist less-experienced team members as needed.
  • Complete required training and participate in site safety programs.
  • Perform routine material handling activities, including lifting and moving items up to 50 lbs.
Qualifications
  • High School Diploma or GED required.
  • 4+ years of experience in pharmaceutical, chemical, biotech, or related manufacturing environments.
  • Experience working in a cGMP-regulated setting.
  • Working knowledge of production control systems and manufacturing operations.
  • Strong troubleshooting, problem-solving, and critical-thinking skills.
  • Highly organized with strong attention to detail and the ability to manage multiple priorities.
  • Ability to work independently while collaborating effectively within cross-functional teams.
  • Comfortable working in a manufacturing environment, including standing for extended periods, wearing required PPE, handling hazardous materials, and lifting up to 50 lbs.
  • Strong written and verbal communication skills.
  • Proficiency in Microsoft Office applications, including Word and Excel.
  • Authorization to work in the United States without current or future sponsorship requirements.

Preferred Qualifications: 

  • Associate degree (Science or technical discipline)
  • Strong mechanical aptitude and desire to execute hands on manual labor
  • Experience with Delta V Production Control System
  • Experience in a Pharmaceutical cGMP manufacturing environment
  • Experience performing large scale distillations / Filtrations / milling
Additional Information
  • After the initial training period of approximately 3 months which will be Monday- Friday from 8am-5pm, team members move to swing shift, which alternates between 1st shift and 2nd shift:

    • 1st Shift is Mon-Fri, 6:00 am to 2 pm

    • 2nd Shift is Mon - Thurs, 2 pm to 12 pm

  • May be requested to work on weekends, overtime, and holidays based on business needs.
  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • LinkedIn: #LI-EB1

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.


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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US