Lab Analyst

Job Details:

Lab Analyst Full details of the job. Vacancy Name Lab Analyst Vacancy No VN586 Department Quality Location Greensboro Employment Type Full-Time Company Overview Aurorium is the materials innovation partner that helps global manufacturers harness the power of possibility making the world a better place. Their specialty ingredients and high-performance materials enhance quality of life, support health and wellness, and enable customers to deliver value-added solutions. Key industries served include healthcare, personal & home care, mobility, infrastructure, and specialty paper & packaging. A Responsible Care® company, Aurorium follows the highest regulatory standards across all manufacturing facilities. The company's global integrated supply chain offers the customer product consistency, easy access, supply security, and reasonable turnaround on delivery. Aurorium is committed to operating at the highest levels of manufacturing consistency, quality control, and safety. Description Lab Analyst is responsible for testing day-to-day raw materials, in-process samples, and finished goods in a pharmaceutical manufacturing environment. This role ensures compliance with cGMP regulations, supports analytical testing activities, and provides technical improvements to the Quality Unit. The QC Analyst plays a key role in maintaining product quality, data integrity, and on-time batch release.

Job Details Role Specific Responsibilities:

Prioritize and coordinate daily QC laboratory activities with the Quality Unit including sample testing, data review, documentation and timely batch release. Perform analytical testing using HPLC, GC, and wet chemistry techniques in accordance with approved methods and specifications. Review and approve analytical data, laboratory notebooks, and test results to ensure accuracy, completeness, and cGMP compliance. Enter results in SAP system Provide technical guidance and training to other team members. Ensure adherence to cGMP, GLP, and data integrity requirements. Support investigations related to out-of-specification (OOS), out-of-trend (OOT), deviations, and corrective and preventive actions (CAPAs). Assist with method verification/validation, transfer, and troubleshooting of analytical methods and

HPLC, GC

equipment. Participate in internal audits, regulatory inspections, and client audits as needed. Collaborate effectively with cross-functional teams including Manufacturing, QA, Supply Chain, Warehouse and EH&S. Maintain laboratory equipment, including qualification, calibration, and preventive maintenance activities. Contribute to continuous improvement initiatives and support laboratory efficiency and compliance goals.

Compliance:

Complies with company Health, Safety and Environmental policies, procedures, and arrangements Reports all Health, Safety and Environmental accidents, incidents and near misses promptly Acts in a safe and responsible manner at all times

Problem Solving and Innovation:

Active participation in continuous improvement activities Participates in problem-solving Takes responsibility and ownership for own learning and development in the spirit of continuous improvement of both self and the business Assists in the training, mentoring, and assessment of other team members Exercises autonomy and judgement subject to overall direction or guidance

Knowledge, Skills, and Abilities:

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline. Strong working knowledge of cGMP regulations and laboratory compliance. Demonstrated ability to operate independently or in a team environment. Minimum of 4 years of experience in a quality control laboratory. 2+ years' experience in a cGMP pharmaceutical organization. Hands-on experience with HPLC, GC, and wet chemistry testing. Experience supporting regulatory inspections (FDA, Food Safety, ISO, etc.). Familiarity with stability testing and method validation activities. Strong communication and interpersonal skills, with the ability to work effectively across teams. Excellent attention to detail and strong problem-solving abilities. Ability to prioritize tasks and manage multiple responsibilities. Proficient in laboratory documentation, data review, and electronic systems (e.g., SAP, LIMS). Capable of making sound technical decisions and escalating issues appropriately. Embodies the core values of

Aurorium:

credible: keeps their word and honors their commitments, acts with integrity, and holds themselves accountable to their decisions and actions outcome-oriented: adheres to an unparalleled standard of excellence in everything they do, to deliver results with real impact driven: passionate about delivering authentic, world-class experiences that engage customers and inspire greatness empowered accountability: empowered to achieve common goals and accountable for delivering performances and results that exceed standard. If you have the energy, drive, and passion for joining the Aurorium team, we would love to hear from you. today! Aurorium offers competitive total compensation packages, including benefits such as medical, dental, vision, life, 401(k), disability insurance, flexible spending accounts, health savings accounts, paid time off, and paid holidays. Aurorium is a global Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of and will not be discriminated against based on gender, sexual orientation, gender identity, race, ethnicity, religion, age, veteran status, disability status, genetic information, or any other protected category. #LI-Onsite