Description

The Quality Investigator/Scientist II will operate in a high-throughput environment, completing investigations on behalf of the various QC testing groups, but primarily for QC Analytical. This person is responsible for leading multiple investigations simultaneously and ensuring on-time completion through dedication, tenacity and relationship building with our partners in QA and the various testing groups. As a strong individual contributor, the Quality Engineer/Scientist III will maintain a steady record closure rate while working on moderate complexity investigations, with some variance in difficulty based on what becomes available. They will also assist more junior investigators when needed and will participate in QC compliance activities related to audits and continuous improvement.

What will you do?

• Stay current with training in Success Factors

• Occasionally conduct RAPID meetings with QA and QC staff

• Use TrackWise software to author investigations

• Be responsible for compliance-related deliverables including: audit support/observation response, presentations to executive management and site leadership, and generating trend reports to better understand the weaknesses in our organization and make suggestions for improvement

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

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

• Assist with the development of tools and resources to improve our 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/revise SOPs (limited)

• Assist with formulating continuous improvement strategies and timelines

• Other job duties as assigned

Skills

GMP, Chemistry, Hplc, Analytical chemistry, Qc, quality control, cgmp, bioassay, uv vis, compendial, enzyme activity assays, enzyme assays, capillary electrophoresis

Additional Skills & Qualifications

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

- Pharmaceutical FDA/GMP regulated environment and working in a QC position

- Experience with HPLC, compendia testing (pH, Osmo, appearance)

- Experience with any bio-assay or biochemistry assays a plus (CGE or iCE)

• TrackWise and TapRooT experience is plus but not required

Knowledge, Skills, Abilities

• Knowledge of GMP regulations

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

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

• Able to use standard computer programs such as SmartSheet, PowerBI, MS Excel, Word, and PowerPoint.

• Able to inspire innovation and team effectiveness.

• Able to work in an evolving environment and adapt to a variety of internal customer’s needs

• Strong computer, scientific, and organizational skills.

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

• Enjoys collaborative efforts both internal and external to the department

#stlsci

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 13, 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 for other accommodation options.