Job Title: Scientist II - Data ReviewJob Description This is an on-site Quality Control position within our Biologics Division located in St. Louis, MO. The Scientist II, Data Review will be responsible for reviewing testing documents generated by the Quality Control Analytical department. They will support programming needs, ensure timely delivery, and evaluate demand versus capacity. The role involves maintaining electronic systems and coordinating with lab managers to resolve testing priorities and timelines. Responsibilities + Review testing carried out by the QC labs, including routine testing, validation, and stability. + Communicate efficiently with peers, QA, and staff to ensure timely corrections of data, resolve issues, and identify when support is required. + Interact with auditors and clients during visits and tours, as needed. + Assist in maintaining data integrity. + Other job duties as assigned. Essential Skills + Experience with HPLC and UPLC, with a minimum of 1-3 years in the quality/analytical/pharmaceutical industry. + Proficiency with a multitude of HPLC/UPLC assays such as SEC, CEX, Glycans, and Peptide Mapping. + Prior use of EMPOWER software. + Knowledge of GMP regulations in a cGMP manufacturing environment. + Working knowledge of scientific principles for a wide range of analytical techniques. + Experience with MS Project, Excel, Word, and Smartsheet. Additional Skills & Qualifications + Bachelor’s degree with 1-3 plus years of relevant work experience. + STEM degree preferred. + Understanding of cGMPs and Quality Control regulatory requirements. + Ability to prioritize multiple timelines and coordinate reviews for multiple testing teams. + Strong presentation skills through various formats (verbal, email, messenger). + Capability to work in a fast-paced environment and prioritize efficiently to meet timelines. Work Environment This role requires working Friday to Monday with 10-hour shifts, and flexibility for shifts from 8-6pm, 10-8pm, and 12-9pm, covering 9am-3pm. The position involves desk work, with 10% standing/walking and 90% sitting at a desk/office. Personal Protective Equipment (PPE) such as lab coats, gloves, eye protection, and safety shoes is required. Exposure to fumes, chemicals, acids, and bases is possible. 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.