Qc Lab Analyst

Actalent; St. Louis (MO); On-site; USD 36,000 - 39,000; Full time

Benefits offered by this job

Medical benefits

401(k)

Life Insurance

PTO

Job summary

Actalent's Saint Louis, MO QC Laboratory Analysts perform analytical testing on raw materials, in-process, and finished product samples in a fast-paced QC lab. The role emphasizes wet chemistry, compendial methods, and data review, with training on HPLC, GC, IR, and UV under supervision.

Second shift, on-site in Saint Louis, MO, with potential overtime and shift flexibility. The position is contract-to-hire, offering growth within a GMP/FDA-regulated environment.

Qualifications

• Bachelor's degree in Chemistry, Biology, or related field required.
• 3 years of QC experience in an FDA-regulated environment preferred.
• Proficiency with wet chemistry or instrumental methods.
• Experience documenting work in GMP/FDA-compliant systems.

Responsibilities

• Perform analytical testing on materials and finished products in QC lab.
• Complete sample preparation with proper labeling and handling.
• Conduct wet chemistry and compendial methods per procedures.
• Document testing activities and results adhering to GMP/FDA requirements.
• Review data for accuracy and compliance with specs.
• Maintain clean, organized lab areas and assist in OOS investigations.
• Learn and perform instrumental analyses (HPLC, GC, IR, UV) under supervision.
• Support production timelines and communicate testing status to team.

Skills

Hands-on Chemistry

Data Recording

Attention to Detail

Analytical Chemistry

FDA GMP Knowledge

Team Collaboration

Flexibility

Education

Bachelors degree in Chemistry, Biology, or related

Tools

HPLC

GC

IR

UV

Job description

Job Title: QC Laboratory Analyst

Job Description

The QC Laboratory Analyst performs analytical testing in a Quality Control laboratory on raw materials, in-process samples, and finished product samples. This role includes full sample preparation, analysis, data review, documentation, and laboratory clean-up, with a primary focus on wet chemistry and compendial methods. Over time, the analyst will be trained on instrumental techniques and will work in compliance with FDA guidelines and GMP documentation standards while supporting investigations into out-of-specification results.

Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished product samples in the Quality Control laboratory.
• Carry out complete sample preparation, including appropriate handling, labeling, and processing of samples prior to analysis.
• Conduct wet chemistry and compendial methods such as pH measurements, titrations, Loss on Drying, and specific rotation according to established procedures.
• Document all testing activities and results accurately and thoroughly in accordance with GMP and FDA regulatory requirements.
• Review and interpret analytical data to ensure accuracy, reliability, and compliance with specifications.
• Maintain clean, organized, and safe laboratory work areas, including performing routine clean-up after testing activities.
• Follow all standard operating procedures and quality guidelines to ensure consistent and compliant laboratory practices.
• Assist in investigations of out-of-specification (OOS) results by providing data, retesting as needed, and contributing to root cause analysis.
• Learn and perform instrumental analyses such as HPLC, GC, IR, and UV under supervision and as training is completed.
• Collaborate with fellow analysts and supervisors to support production timelines and minimize delays caused by testing.
• Remain on-site beyond scheduled shift when necessary to complete critical procedures and prevent production hold-ups.
• Participate in cross-training across different test methods and product types to gain broad exposure to all aspects of QC testing.
• Support continuous improvement efforts in laboratory processes, documentation practices, and analytical techniques.
• Communicate effectively with team members regarding testing status, issues encountered, and results requiring follow-up.

Essential Skills

• Demonstrated hands-on chemistry laboratory experience gained through academic work or industry employment.
• Proficiency with wet chemistry techniques including titrations, pH measurement, Loss on Drying, and related compendial methods.
• Experience or familiarity with quality control testing in a laboratory environment.
• Understanding of analytical chemistry principles and their application to QC testing.
• Ability to follow FDA guidelines and document work in accordance with GMP requirements.
• Strong attention to detail in sample preparation, data recording, and documentation.
• Capability to assist with investigations of out-of-specification results by providing accurate data and participating in analysis.
• Basic knowledge of instrumental methods such as HPLC, GC, IR, and UV, or the ability to learn these techniques quickly.
• Effective time management skills to meet testing timelines and support production needs.
• Willingness to remain beyond scheduled shift when necessary to complete critical procedures.

Additional Skills & Qualifications

• Bachelors degree in Chemistry, Biology, or a related scientific discipline.
• 03 years of quality control experience in an FDA-regulated environment, preferably in pharmaceuticals or consumer products operating under GMP.
• Proficiency demonstrated with wet chemistry or instrumental methods, clearly reflected in prior experience or academic background.
• background in analytical chemistry or biology that supports understanding of QC testing requirements.
• Interest in gaining broad exposure to a wide range of analytical techniques rather than focusing on a single type of testing.
• Ability to work effectively as part of a small, collaborative team.
• Adaptability to a fast-paced yet manageable environment with evolving priorities.

Work Environment

This role is based in a spacious, recently renovated and modernized QC laboratory that serves as a hub for testing across multiple sites. The position is on a second shift schedule, Monday through Friday from approximately 2:00 p.m. to 10:30 p.m., with potential flexibility of 3060 minutes on start time. Occasional overtime may be required a few times per month to complete procedures and avoid delays in production.

Job Type & Location

This is a Contract to Hire position based out of Saint Louis, MO.

Pay and Benefits

The pay range for this position is $26.00 - $28.00/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)

• 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 Saint Louis,MO.

Application Deadline

This position is anticipated to close on Oct 14, 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.