URGENTLY HIRING INTERESTED CANDIDATES EMAIL RESUMES TO DASILVA @ Job Title: Stability Technician Job Description The Stability Technician supports pharmaceutical stability programs by managing samples, maintaining accurate electronic records, and ensuring compliance with cGMP, FDA regulations, standard operating procedures, and work instructions. This role focuses on initiating, tracking, and maintaining stability studies in laboratory systems while coordinating with multiple departments to ensure timely testing and proper inventory control. Responsibilities + Ensure stability studies are initiated, placed, and maintained in accordance with cGMP, FDA regulations, SOPs, work instructions, and applicable guidelines. + Apply working knowledge of cGMP, FDA regulations, SOPs, and work instructions to start studies correctly and maintain regulatory compliance throughout the study lifecycle. + Perform daily stability sample pulling and ensure appropriate laboratories receive samples on or before testing due dates. + Initiate and maintain stability studies through LIMS to support annual and ongoing stability program requirements. + Maintain up-to-date inventory for all stability studies using LIMS and other inventory management tools. + Initiate and coordinate the destruction and reconciliation of non-class and class samples via LIMS in accordance with procedures. + Pull samples from quality chambers, maintain retain samples, and sort samples according to study requirements. + Assist with stocking, sorting, organizing, and moving samples, totes, and related materials to support laboratory and stability operations. + Log data and sample information accurately into SAP, Labware, and inventory management systems. + Follow established documentation processes to ensure complete, accurate, and compliant records for all sample and stability activities. + Support quality control activities through careful inspection, verification, and documentation of samples and related data. + Collaborate with team members and other departments to ensure smooth sample flow, timely testing, and effective communication. + Adhere to all safety, quality, and compliance procedures while working with multiple products, reagents, and drugs in a chemical stockroom environment. Essential Skills + High school diploma or equivalent. + 1u20132 years of relevant industry experience in sample management, quality, or regulatory work. + Working knowledge of cGMP principles and quality control practices. + Ability to follow and apply FDA regulations, SOPs, and work instructions in daily work. + Experience with sample preparation, documentation processes, and quality inspection activities. + Strong attention to detail and organizational skills to manage multiple studies and inventories accurately. + Strong communication skills to interact effectively with team members and cross-functional departments. + Comfort working on your feet for the majority of the shift and walking between multiple departments. + Comfort using different software systems and basic to intermediate computer skills. + Ability to work accurately within LIMS, SAP, Labware, and inventory management systems after training. Additional Skills & Qualifications + Associate or bacheloru2019s degree in a science or regulatory-related field is welcome but not required. + Experience as a pharmacy technician, lab assistant, or in a similar laboratory support role is beneficial. + Prior inventory management experience is a plus. + Experience in quality control, quality inspection, or regulated pharmaceutical environments is advantageous. + Familiarity with handling multiple products, reagents, and drug materials in a controlled setting. + Demonstrated ability to sort, organize, and track samples efficiently in a fast-paced environment. Work Environment This role is based in a chemical stockroom environment within a large pharmaceutical manufacturing facility, working with multiple products, reagents, and drugs. You will work closely with a small core team of about four people while collaborating frequently with many other departments on site. The position follows a first-shift schedule, Monday through Friday, typically 7:00 a.m. to 3:30 p.m., with flexibility to work an alternative schedule such as 9:00 a.m. to 5:30 p.m. as needed. The dress code is business casual, including slacks or jeans, closed-toe shoes with high socks, and a polo or shirt without large graphics. The work requires being on your feet for much of the day and walking between various departments, using computer systems such as LIMS, SAP, Labware, and inventory management tools in a structured, process-driven environment that emphasizes safety, quality, and internal growth opportunities. Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $21.00 - $21.00/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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on May 1, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is 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 Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, weu2019ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACu2014with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at .
Job Title
Senior Technician