Description
\t\t\t\t\t1 year for QC Scientist I 5 years for Scientist II and 8 plus years of experience for Scientist IIIPosition reports to the St Louis, MO site, and supports the Drug Substance Division.Discover Impactful Work:In this role you will use numerous analytical tools used for large molecule analysis, such as HPLC, UPLC, CGE, iCE, Cell Based Analyses, Compendial Testing (pH, UV, Osmolality, Appearance), and other minor equipment. This work will be supporting GMP manufacturing for commercial product testing along with Stability testing and other endeavors requested by the client. This role will require experience in working in a cGMP environment.A Day in the Life:• 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 delivery for projects.• 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, Titer concentration, CEX, etc)• Compiles data for documentation of test procedures, prepares reports. Collaborate with team members and other departments such as quality assurance and data reviewers.• Contributes 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; 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.
\t\t\t\t\tSkills
\t\t\t\t\tHPLC, GMP, chemistry, EMPOWER, Quality control, analytical chemistry, wet chemistry, cgmp
\t\t\t\t\tTop Skills Details
\t\t\t\t\tHPLC,GMP,chemistry,EMPOWER
\t\t\t\t\tAdditional Skills & Qualifications
\t\t\t\t\tKeys to Success:Education• Required: Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology or related field.Experience• At least 1-year proven experience in a regulated field is required in a similar, or related job function.Knowledge, Skills, Abilities• In-depth knowledge of the most common analytical techniques and required instrumentation (HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, cell based bioassays, etc..).• Knowledge of MS Office and laboratory computer programs.Personality traits:• Flexibility.• Good organization and planning skills.• Attention to details.• Positive and collaborative demeanour.
\t\t\t\t\tExperience Level
\t\t\t\t\tIntermediate Level
Pay and Benefits
The pay range for this position is $30.00 - $50.00/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 St. Louis,MO.
Application Deadline
This position is anticipated to close on Mar 13, 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 & InclusionAt 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 peopleThe 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.