Analyst III, QC Laboratory Services-3rd Shift

About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain. Job Summary This role will be responsible for performing analytical testing per cGMP in support of Bora raw material, in-process, final product, stability, and method transfer testing. This position will support our 3rd-shift Operations, working 10pm-6:30am, Monday - Friday. Eligible for shift differential. Essential Functions Reasonable accommodations will be provided to enable individuals with disabilities to perform the essential functions. Perform various analytical testing procedures as per manufacturing/Quality Control batch records, Stability Protocols, etc. Execute complex methods requiring difficult sample preparation or data analysis. Assist with the design of method validations and execute validation studies, including method transfer activities. Work with Project Managers and QA to ensure timely testing and release of samples. Perform instrumental analysis such as Karl Fischer, UV, HPLC, and Gas Chromatography. Inform supervisor upon observing out-of-specification (OOS) results. Participate in investigations of OOS results and other related studies. Participate in calibration and troubleshooting of various types of equipment, including proactive resolution of instrument issues. Write protocols and reports as necessary. Plan and execute experimental tasks and obtain and interpret experimental data with minimal guidance. Perform review of calculations, logbooks, and other data to execute LIMS approval, lot release protocols, and final product data authorizations or approvals. Write and review SOPs and Testing Standards as necessary. Interact with clients as necessary regarding cGMP, tech transfer methods, or stability issues. Assist in training other Analysts. Review, analyze, interpret, and report data. Verify and enter approved results in LIMS. Practice good documentation and laboratory safety procedures per Standard Operating Procedures. Support department compliance and productivity goals. Track time worked per project. Training and education may be conducted using virtual reality/artificial intelligence. Participate in meetings as required. The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions. Minimum Education, Experience and Skills B.S. in Chemistry, Biochemistry or other Technical Science field required with minimum of 3-5 years in a cGMP laboratory required or master's degree with 2 years of laboratory experience required. Demonstrated knowledge of wet chemistry, titration, UV and chromatography. GLP/GMP experience required. HPLC/GC/IC Chromatography experience is required. Knowledge of new and existing testing applications. Salary Range: 88,000 - 115,000 Compensation and Benefits We offer a comprehensive benefits package designed to support our employees’ wellbeing, including: Competitive salary and performance-based incentives Comprehensive health coverage including medical, dental, and vision insurance Retirement savings plans with employer matching contributions Paid time off Professional development opportunities Employee wellness programs and resources Employee Assistance Program and Mental Health Resources Core Values At Bora, our values guide everything we do — from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone. Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category. Bora Pharmaceuticals is focused on developing and manufacturing branded, generic and over the counter (OTC) healthcare and pharmaceutical products for patients around the globe. At Bora Pharmaceuticals, we see it as our mission and our duty to make our mutual success more certain. As an ambitious, future-focused company, we know better than most that our own success is shaped by our partners victories. Not finding the right fit? Let us know you're interested in a future opportunity by clicking Get Started below or create an account by clicking 'Sign In' at the top of the page to set up email alerts as new job postings become available that meet your interest!