Scientist

Actalent; Clinton (IN); On-site; USD 69,000 - 76,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Job summary

Actalent is seeking a dedicated Scientist to support analytical laboratory operations, focusing on HPLC/LC method transfers in a GMP-regulated environment. The successful candidate will utilize the Empower chromatography data system to execute method transfer protocols, perform analytical testing, and document analytical data in GMP settings.

The onsite Clinton, IN facility requires collaboration with QA, Development, IT and site personnel to drive project execution, while adhering to DEA

Qualifications

• 3–5 years in pharmaceutical/biotech analytical labs.
• Experience with DEA-controlled substance testing preferred.
• Familiarity with FDA GMP regulations and laboratory compliance.
• Proficient with MS Office and lab documentation systems.

Responsibilities

• Execute HPLC/LC methods transfers using Empower CDS.
• Prepare samples, standards, mobile phases, and reagents.
• Perform analytical testing and complete verification runs.
• Review chromatographic data against acceptance criteria.
• Document testing activities in GMP-compliant records.
• Support method verification, reporting, and transfer documentation.
• Complete required training for DEA-controlled substance handling.

Skills

HPLC/LC testing

Empower CDS

Analytical method execution

Sample preparation

Data review & interpretation

Method transfer & verification

GMP documentation

Laboratory investigations & quality

Prioritization of testing

Cross-functional collaboration

Education

Bachelor's degree in Chemistry/Biochemistry/Pharmaceutical Sciences

Tools

Empower CDS

Job description

Job Title: Scientist

Job Description

We are seeking a dedicated Scientist to support our analytical laboratory operations, focusing on HPLC/LC method transfers. The successful candidate will utilize the Empower chromatography data system to execute method transfer protocols, perform analytical testing, and document analytical data in a GMP-regulated environment.

Responsibilities

• Execute HPLC/LC method transfer protocols using the Empower CDS.

• Perform sample and reagent preparation, and conduct analytical testing activities.

• Complete analytical runs, replicates, and protocol-defined verification testing.

• Review chromatographic data to ensure results meet established acceptance criteria.

• Document testing activities and results in compliance with GMP requirements.

• Support method verification, report generation, and transfer documentation.

• Complete required training for DEA-controlled substance handling and testing.

• Assist with the implementation of additional analytical methods and laboratory expansion.

• Support increased testing capacity through routine laboratory testing activities.

• Collaborate with Quality Assurance, Development, IT, and site personnel for successful project execution.

• Participate in laboratory status meetings and provide project updates.

• Support final reporting, knowledge transfer, and project closeout activities.

Essential Skills

• Hands-on HPLC/LC laboratory testing experience.

• Experience with Empower chromatography data system.

• Ability to execute analytical test methods following approved protocols and SOPs.

• Experience in preparing samples, standards, mobile phases, and reagents.

• Ability to review chromatographic data and interpret analytical results.

• Understanding of method transfer, verification, and reproducibility requirements.

• Experience in a GMP-regulated pharmaceutical or biotechnology environment.

• Ability to maintain accurate laboratory documentation and data integrity.

• Knowledge of laboratory investigations, deviations, and quality systems.

• Ability to manage multiple testing priorities while ensuring high-quality execution.

Additional Skills & Qualifications

• Minimum 3 to 5 years of experience in pharmaceutical, biotechnology, or analytical laboratories.

• Minimum 2+ years of hands-on HPLC/LC testing experience.

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, or a related scientific discipline preferred.

• Experience with DEA-controlled substance testing or willingness to complete qualifications preferred.

• Experience supporting method transfer, method validation, or method verification projects preferred.

• Knowledge of FDA GMP regulations and laboratory compliance requirements.

• Proficiency with laboratory documentation systems and Microsoft Office applications.

• Experience supporting laboratory scale-up, increased testing capacity, or new method implementation is a plus.

Work Environment

The position is onsite at a dedicated facility, offering a fast-paced laboratory environment with changing priorities. The work involves collaboration across multiple departments, ensuring a dynamic and supportive team atmosphere.

Job Type & Location

This is a Contract position based out of Clinton, IN.

Pay and Benefits

The pay range for this position is $50.00 - $55.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Benefits available for this temporary role may include the following:

• 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 Clinton,IN.

Application Deadline

This position is anticipated to close on Sep 19, 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.