QC Investigator II

Actalent • Berkeley, MO • 10h ago

Job Title: QC Investigator II

Job Description

The Quality Investigator/Scientist II plays a pivotal role in a high-throughput environment, conducting investigations primarily for QC testing groups. This individual is responsible for leading multiple investigations simultaneously, ensuring timely completion through dedication, tenacity, and relationship building with QA partners and various testing groups. As a strong individual contributor, the Quality Engineer/Scientist III maintains a consistent record closure rate while working on moderately complex investigations. Additionally, they assist junior investigators and participate in QC compliance activities related to audits and continuous improvement.

Responsibilities

Stay current with training in Success Factors.

Conduct RAPID meetings with QA and QC staff occasionally.

Use TrackWise software to author investigations.

Be responsible for compliance-related deliverables, including audit support, observation response, presentations to management and site leadership, and generating trend reports.

Support compliance culture initiatives and assist manager and supervisor with implementing changes.

Develop the team through creation and delivery of proactive and reactive trainings.

Assist with the development of tools and resources to improve the investigative process.

Assist Scientist I investigators when needed.

Average 3-4 deviation/OOS/CAPA record closures per month, based on complexity.

Complete overdue assessments and file record extensions as required.

Author and revise SOPs, as needed.

Assist with formulating continuous improvement strategies and timelines.

Other job duties as assigned.

Essential Skills

GMP regulations knowledge.

Chemistry and analytical chemistry expertise.

Pharmaceutical QC experience with HPLC.

Compendial Testing (pH, UV, Osmolality, Appearance).

Experience in OOS/OOT investigations.

Bachelor's degree in science-related field with 3-4 years of industry experience.

Experience in a pharmaceutical FDA/GMP regulated environment.

Proficiency in QC position requirements.

Knowledge of Good Laboratory Practices (GLP) and Good Documentation Practices (GDP).

Strong computer, scientific, and organizational skills.

Additional Skills & Qualifications

SoloVPE, qPCR, color metric-based assays (Picogreen, Bradford).

Experience with enzyme activity assays and spectrometer or plate readers.

Qualitative pipetting and multi-channel pipetting experience.

Prior use of EMPOWER or TrackWise.

Experience with bioassay, UV Vis, enzyme activity assays, capillary electrophoresis.

Able to read, write, and communicate effectively in English.

Proficiency in standard computer programs such as SmartSheet, PowerBI, MS Excel, Word, and PowerPoint.

Ability to inspire innovation and team effectiveness.

Ability to work in an evolving environment and adapt to various internal customer needs.

Strong communication skills including active listening, facilitation, and escalation.

Enjoys collaborative efforts both internal and external to the department.

Work Environment

This role requires onsite training, with the option to work one day from home once trained. It involves wearing gloves and other PPE to enter laboratory spaces and requires sitting for extended periods due to desk and meeting time. The team consists of four members and a supervisor. The position will have an initial phase of 3-6 months of hands-on training.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $32.00 - $37.00/hr.

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 Berkeley,MO.

Application Deadline

This position is anticipated to close on Feb 22, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

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