URGENTLY HIRING: QC Scientist II

Actalent; Columbus (OH); On-site; USD 80,231,000 - 85,962,000; Full time

Job summary

Actalent in Columbus, OH seeks a QC Scientist II to perform qualitative and quantitative testing with HPLC, GC, and wet chemistry in a GMP/FDA-regulated setting. The role emphasizes method execution, data integrity, and investigations in a fast-paced pharmaceutical environment.

You will prepare samples, document results, and collaborate with quality and manufacturing teams to ensure product quality and compliance.

Qualifications

• Bachelors or Masters in chemistry/biochemistry.
• 23+ years of industry experience in a chemistry laboratory environment.
• Hands-on experience with HPLC or GC; strong proficiency in at least one of these techniques.
• Experience working in a GMP and FDA-regulated environment.

Responsibilities

• Perform qualitative and quantitative testing for APIs, starting materials, packaging components, and finished products.
• Prepare samples and dilutions to ensure accurate analytical results.
• Operate HPLC, GC, and wet chemistry methods following GMP procedures.
• Peer review analytical documentation and resolve discrepancies to uphold quality standards.
• Maintain organized, traceable laboratory data and controlled documents.

Skills

Analytical chemistry

GMP awareness

Data integrity

Written/verbal communication

Team collaboration

Multi-tasking

Education

Bachelor's or Master's in Chemistry or Biochemistry

Tools

HPLC

GC

Job description

Job Description

The QC Scientist II performs a broad range of qualitative and quantitative chemical and physical testing to support active pharmaceutical ingredients, starting materials, packaging components, and finished products in a regulated laboratory environment. This role focuses on analytical method execution and improvement, data integrity, and quality investigations, while working with advanced instrumentation such as HPLC, GC, and wet chemistry techniques in a fast-paced pharmaceutical manufacturing setting.

Responsibilities

• Perform qualitative and quantitative chemical and physical testing in accordance with compendial requirements and product specifications for active pharmaceutical ingredients, starting materials, packaging components, and finished products.
• Prepare samples, including dilutions and other sample preparation techniques, to ensure accurate and reliable analytical results.
• Conduct testing using HPLC, GC, wet chemistry, and other analytical methods, following established procedures and Good Manufacturing Practices (GMP).
• Perform peer review of analytical testing documentation, identify discrepancies, and work to resolve them in compliance with quality standards.
• Maintain laboratory data in an organized and traceable manner in laboratory notebooks, worksheets, and controlled documents.
• Re-validate chemistry methods as required, ensuring methods remain robust, accurate, and compliant with regulatory and internal standards.
• Author clear and concise technical reports to support analytical method improvements, investigations, and troubleshooting activities.
• Perform investigational and troubleshooting analyses, including advanced analytical techniques, to support approved commercial testing and resolve laboratory or production issues.
• Apply knowledge of critical functions and variables for each type of laboratory equipment and demonstrate strong instrument troubleshooting ability.
• Complete and conduct required training according to the laboratory curriculum and maintain up-to-date qualifications on relevant methods and equipment.
• Work independently while actively contributing to a team-based approach to accomplish assigned tasks and project objectives.
• Manage multiple projects and tasks simultaneously in a fast-paced environment, effectively prioritizing workload to meet deadlines.
• Communicate findings, results, and issues clearly through strong written and verbal communication with colleagues across quality and manufacturing groups.
• Collaborate with quality teams to support investigations and continuous improvement activities related to analytical testing and product quality.
• Demonstrate sound scientific judgment and professional competency while working under supervision to execute and interpret laboratory work.

Essential Skills

• Bachelors or Masters degree in a scientific field, with a preference for Chemistry or Biochemistry.
• 23+ years of industry experience in a chemistry laboratory environment.
• Hands‑on experience with HPLC or GC; strong proficiency in at least one of these techniques is required.
• Experience working in a quality function and participating in quality investigations.
• Proficiency with sample preparation techniques, including dilutions and related laboratory practices.
• Experience working in a GMP and FDA‑regulated environment.
• Ability to work effectively in a team environment to accomplish assigned tasks.
• Ability to manage and work on multiple tasks in a fast‑paced environment.
• Strong written and verbal communication skills.
• Ability to work with supervision while applying scientific judgment and professional competency in daily activities.
• Solid understanding of chemistry and biochemistry principles as applied to pharmaceutical quality control.
• Ability to troubleshoot laboratory instruments and methods using a structured, scientific approach.

Additional Skills & Qualifications

• Experience with both HPLC and GC is highly beneficial, even though strong expertise in one technique is acceptable.
• BG in biochemistry or related disciplines supporting analytical testing of pharmaceutical products.
• Familiarity with quality control processes in large‑scale pharmaceutical manufacturing environments.
• Experience authoring technical reports and documentation to support method improvement and investigations.
• Comfort working across both quality control laboratories and manufacturing areas to support end‑to‑end product quality.
• Demonstrated ability to adapt to organizational change and take advantage of growth and upward mobility opportunities.

Work Environment

This role is based in a fast‑paced pharmaceutical manufacturing and quality environment, with time spent primarily in the quality control laboratory and occasional work in the manufacturing area. You will regularly work with analytical instruments such as HPLC and GC, along with wet chemistry techniques, within a GMP and FDA‑regulated setting that emphasizes data integrity, safety, and compliance. The standard schedule is first shift, Monday through Friday, 7:00 a.m. to 3:30 p.m., with some flexibility. The position starts on a 5x8‑hour schedule, and after completing initial training, there is an opportunity to move to a 4x10‑hour schedule. Training will occur on first shift for the first one to two months. The culture promotes growth and internal advancement, offering ample opportunity for professional development and upward mobility following a recent organizational restructuring.

Job Type & Location

This is a Contract to Hire position based out of Columbus, OH.

Pay And Benefits

The pay range for this position is $28.00 - $30.00/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.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the 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 Columbus,OH.

Application Deadline

This position is anticipated to close on Oct 18, 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.