QC Scientist

Job Description

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

Responsibilities

• Perform HPLC, UPLC, CGE, iCE, Cell-Based Analyses, Compendial Testing (pH, UV, Osmolality, Appearance), 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 (i.e., Reverse Phase, SEC, protein concentration, CEX, etc.).
• 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, perform safety inspections, and order supplies.

Essential Skills

• Proven experience in a GMP regulated environment (1-5 years), preferably pharmaceuticals.
• Experience with analytical techniques and required instrumentation (HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, cell-based bioassays, etc.).
• Prior use of EMPOWER is preferred.
• Knowledge of GMP regulations in a cGMP manufacturing environment.
• Working knowledge of scientific principles for a wide range of analytical techniques.
• Quality control and analytical chemistry expertise.

Qualifications

• Bachelor’s degree in chemical, pharmaceutical, biology, chemistry, biotechnology, or related field.
• Knowledge of MS Office and laboratory computer programs.
• Flexibility, good organization and planning skills, attention to details, positive and collaborative demeanor.

Work Environment

This role is part of a newly formed team of 7 within the QC Analytical team, which has over 80 members. You will have a supervisor and 6 team members. The role includes 3-6 months of training and requires testing on each test before moving to the next. You will work in a pharmaceutical lab setting doing bench work.

Pay and Benefits

The pay range for this position is $30.00 - $45.00/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 Mar 10, 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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

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 actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $30 - $45