Job Title: Quality TechnicianJob DescriptionnnThe Quality Technician performs essential duties to ensure the Stability Program operates effectively and complies with US and International pharmaceutical manufacturing regulations and guidance documents. Responsibilities include the packaging, storage, and delivery of stability material in a timely manner, updating department Work Instructions or site Quality System Procedures, and developing solutions to routine technical problems to improve department efficiencies.nnResponsibilitiesnnManage and maintain stability samples under ICH, FDA, DEA, and cGMP regulations.nnPull and deliver stability samples at testing intervals.nnPackage stability samples per study requirements.nnMaintain controlled substance inventory in compliance with applicable DEA regulations.nnWork with the LIMS team to ensure the stability module of the LIMS system is maintained and functional.nnEnsure stability studies are entered into LIMS accurately and timely.nnResponsible for packaging, labeling, and storage of stability samples.nnShare responsibility for Stability Packaging functions and sample pulls as needed.nnEssential Skillsnn6 months-1 year of industry experience within GMP.nnLab experience with laboratory notebook experience and aseptic experience.nnBS degree in Biology or Chemistry preferred, but not required.nnExperience with quality control, Microsoft Office, and data entry.nnAdditional Skills & QualificationsnnSome technical, community college, or college credits with 1-year related experience in lab, GMP.nnPreferred: BS Degree in Science with laboratory experience and interest in working in Stability.nnKnowledge of pharmaceutical regulations including current GXP, GLP, or GMP requirements.nnExcellent communication skills.nnAbility to work in and promote a team environment.nnUnderstanding and application of principles, concepts, practices, and standards within discipline.nnKnowledge of stability chambers and laboratory equipment.nnAbility to read and interpret graphs.nnAbility to lead and influence people.nnUnderstanding of basic statistical principles.nnKnowledge of ELN, LIMS, Excel, and MiniTab.nnWork EnvironmentnnThe position involves 50% laboratory exposure to plant products, solvents, and reagents, some of which are hazardous or potent compounds, and 50% office environment which includes sitting for long periods of time and computer use. The role does not require a respirator but will involve working in safety hoods with packaging stability products. The work schedule is Monday-Friday.nnAbout ActalentnnActalent 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.nnDiversity, Equity & InclusionnnAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:nnHiring diverse talentnnMaintaining an inclusive environment through persistent self-reflectionnnBuilding a culture of care, engagement, and recognition with clear outcomesnnEnsuring growth opportunities for our peoplennThe 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.nnIf 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 (% ) for other accommodation options.