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Job Title: QC ScientistJob Description

In this role, you will utilize a variety of analytical tools for large molecule analysis, including HPLC, UPLC, CGE, iCE, Cell Based Analyses, and Compendial Testing (pH, UV, Osmolality, Appearance). Your work will support GMP manufacturing for commercial product testing, stability testing, and other client-requested projects. Experience in a cGMP environment is required.

Responsibilities

+ Perform HPLC, UPLC, CGE, iCE, Cell Based Analyses, Compendial Testing, and other minor equipment testing on In-Process, DS release, and stability samples, ensuring timely project delivery.

+ Review laboratory data packets as assigned.

+ Perform and author laboratory investigations as assigned.

+ Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods.

+ Compile data for documentation of test procedures and prepare reports.

+ Collaborate with team members and other departments such as quality assurance and data reviewers.

+ Contribute to the development of new concepts, techniques, and standards.

+ Recognize and report invalid/lab incident/out-of-specification/out-of-trend results to laboratory management and recommend solutions.

+ Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines.

+ Participate in laboratory activities, performing safety inspections and ordering supplies.

Essential Skills

+ 0-5 years of proven experience in a GMP regulated environment, preferably pharmaceuticals.

+ Experience with analytical techniques and required instrumentation (HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, cell-based bioassays).

+ Knowledge of GMP regulations in a cGMP manufacturing environment.

+ Working knowledge of scientific principles for a wide range of analytical techniques.

+ Knowledge of EMPOWER and MS Office and laboratory computer programs.

Additional Skills & Qualifications

+ Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology, or related field.

+ Flexibility, good organization and planning skills, attention to detail, and a positive and collaborative demeanor.

+ Prior use of EMPOWER is preferred.

Work Environment

This role is part of a newly formed team of 6 Scientists and 1 Supervisor to support the weekend shift within the QC Analytical team, which consists of over 80 members. You will undergo 3-6 months of training, testing on each test before progressing to the next. Work will take place in a pharmaceutical lab setting with bench work. The position requires working 4-10 hour shifts from Friday to Monday, with flexible hours from 7am-5pm or 8am-6pm. Training will initially occur Monday-Friday before transitioning to the weekend schedule.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $28.00 - $38.00/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 Nov 3, 2025.

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 [email protected] (%[email protected]) for other accommodation options.