Chemist

Actalent; Lincoln (NE); On-site; USD 37,000 - 40,000; Full time

Benefits offered by this job

Health benefits

401(k) plan

Life Insurance

Disability coverage

HSA

Commuter benefits

Employee Assistance Program

PTO/Vacation

Job summary

Actalent is seeking a Chemist for our Lincoln, NE QC laboratory to perform analytical testing of raw materials and finished products using HPLC, GC, UV–VIS, and wet chemistry techniques. You will ensure data integrity by precise documentation and adherence to CGMPs and FDA/EU guidelines.

The role requires a four-year degree in Chemistry or Biochemistry and 2+ years of lab experience, comfortable operating CDAS and LIMS, and collaborating in a fast-paced, high-volume environment.

Qualifications

• Four-year degree in Chemistry or Biochemistry with 2+ years of analytical lab experience.
• Experience with HPLC, GC and UV−VIS in a QC/regulated environment.
• Knowledge of CGMPs and FDA/EU guidelines applicable to lab testing.

Responsibilities

• Perform analytical testing of materials and finished products using established procedures.
• Operate and maintain HPLC, GC, UV−VIS and other lab instruments.
• Use LIMS and CDAS to acquire, process, and manage data.
• Adhere to SOPs, CGMPs and regulatory guidelines in all testing activities.
• Document results and deviations accurately and thoroughly.
• Collaborate with lead analysts to resolve issues and improve methods.

Skills

HPLC

GC

UV-VIS

Wet chemistry

Documentation

CGMPs

FDA/EU guidelines

LIMS

CDAS

Team collaboration

Education

Bachelor's degree in Chemistry or Biochemistry

Tools

Waters Empower

LIMS

CDAS

Job description

Job Description

This Chemist position focuses on analytical testing of raw materials and finished pharmaceutical and biological products in a regulated quality control laboratory. You will perform a wide range of analytical techniques using advanced instrumentation and data systems while ensuring strict compliance with CGMPs, Standard Operating Procedures, and global regulatory guidelines. This role offers the opportunity to work in a collaborative chemistry lab that supports a growing manufacturing site and plays a critical part in releasing products to market.

Responsibilities

• Perform analytical testing of raw materials and finished pharmaceutical and biological products using established test procedures.
• Operate and maintain analytical instrumentation, including HPLC, GC, UV-VIS, and other relevant laboratory equipment.
• Use Computer Data Acquisition Systems (CDAS) and Laboratory Information Management Systems (LIMS) to acquire, process, and manage analytical data.
• Follow Standard Operating Procedures (SOPs), CGMPs, company quality standards, and FDA/EU guidelines in all testing activities.
• Adhere to testing schedules to complete a high volume of critical work without compromising data integrity or quality.
• Conduct wet chemistry techniques such as titration and pipetting accurately and consistently.
• Perform accurate and thorough documentation of all laboratory activities, test results, observations, and deviations.
• Review documentation for completeness, accuracy, and compliance with regulatory and internal standards.
• Apply knowledge of human error awareness and prevention to minimize mistakes and maintain data reliability.
• Participate in investigations and problem-solving activities related to laboratory results, methods, or equipment issues.
• Communicate effectively with lead analysts and colleagues to coordinate work, clarify requirements, and resolve issues.
• Collaborate as part of a team in a busy QC laboratory environment, supporting colleagues and contributing to shared goals.
• Adjust priorities and switch tasks quickly when needed to meet turnaround times and deadlines for product release.
• Ensure laboratory areas and equipment remain clean, organized, and in a state of readiness for testing.
• Contribute to continuous improvement initiatives in laboratory processes, documentation practices, and analytical methods.

Essential Skills

• Experience in an analytical chemistry testing laboratory performing wet chemistry and instrumental analysis.
• Hands‑on experience with HPLC, including method execution and troubleshooting, required.
• Experience with GC and UV‑VIS instrumentation in a laboratory setting.
• Proficiency in accurate laboratory techniques such as titration and pipetting.
• Ability to perform precise and compliant documentation of laboratory work and results.
• Strong organizational skills to manage multiple tests, samples, and deadlines in a high‑volume environment.
• Effective written and verbal communication skills for working with lead analysts and colleagues.
• Ability to work collaboratively as part of a team and maintain a positive, professional attitude.
• Working familiarity with Microsoft Word and Excel for data recording, reporting, and communication.
• Knowledge of CGMPs, SOPs, and FDA/EU regulatory expectations in a laboratory environment.
• Working knowledge of the US and European pharmacopeia.
• Four‑year degree in Chemistry or Biochemistry with two or more years of analytical chemistry laboratory experience.
• Ability to manage stress and maintain accuracy when working under strict turnaround times and deadlines.
• Capability to adapt quickly and switch tasks as priorities change in a QC lab setting.

Additional Skills & Qualifications

• Bachelor of Science in Chemistry or Biochemistry preferred.
• Operational experience with Waters Empower data acquisition software preferred.
• Experience working in an FDA, USDA, or EU regulated laboratory environment.
• Knowledge of human error awareness and prevention techniques.
• Experience in investigation and problem‑solving related to laboratory results or processes.
• Experience with LIMS and CDAS for data acquisition and sample management.
• Familiarity with liquid chromatography and related analytical techniques.
• Demonstrated ability to maintain a positive attitude in a fast‑paced, deadline‑driven environment.

Work Environment

This role is based in a regulated FDA/USDA/EU laboratory environment within a quality control chemistry lab of approximately 40 people. The lab is organized into three primary areas: raw material testing, biological testing, and pharmaceutical testing, with all work focused on quality control of incoming raw materials and finished products from manufacturing. Because the lab serves as the final stage before products can be released and shipped, there are frequent turnaround times and deadlines, and the environment can be fast‑paced and occasionally stressful. Team members may need to switch priorities quickly to meet testing schedules and support product release. The lab uses advanced analytical technologies such as HPLC, GC, UV‑VIS, CDAS, LIMS, and related software tools. Standard hours are Monday through Friday, 8:00 AM to 5:00 PM. The culture emphasizes collaboration, teamwork, and a supportive group of colleagues, with opportunities for growth as the site expands and brings new products into the plant.

Job Type & Location

This is a Contract to Hire position based out of Lincoln, NE.

Pay And Benefits

The pay range for this position is $27.00 - $29.00/hr.

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lincoln,NE. Application Deadline This position is anticipated to close on Sep 21, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News‑Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.