Quality Specialist - II - Rotating Shift

Education Minimum Requirements
• Bachelor's degree in Chemistry, Biology, Biochemistry or other scientific discipline
Required Experience and Skills
• Minimum two years of quality or laboratory experience in pharmaceutical industry, or advanced degree
• Capable of working shift work (12 hours shifts with daylight and night shift coverage)
• Effective communication and decision making skills
• Experience with laboratory instrumentation and bench testing
Preferred Experience and Skills
• Previous experience with laboratory data management systems
• Proficient in operating and troubleshooting laboratory instrumentation
Note:
• This position operates on a 12-hour rotating shift, with third shift and weekend coverage.
• Work Schedule: 12 hour rotating shift; days and nights (7am-7pm or 7pm-7am).
• IMPORTANT: ** Expected to work in an environment with potential beta-lactam antibiotic exposure **
Job Description:
Our Quality Control group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements.
Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers, we create an interdependent global manufacturing network dedicated to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.
The shift supervisor will supervise a team of laboratory technicians performing analytical testing on in-process and water samples. Instrumentation includes KF, IR, GC, HPLC, UPLC, and others. This position routinely participates in laboratory related activities such as second person review of the laboratory technicians work, microplate assay testing, and instrument troubleshooting.
This position operates on a 12-hour rotating shift, with third shift and weekend coverage.
Primary Responsibilities
• Performs second person review of in-process and water sample testing using methods such as GC, TOC, conductivity, titrations, turbidimetric spectroscopy, and microbial filtration
• Performs review of paper documents as well as review of electronic records
• Assists with laboratory GMP activities by performing instrument troubleshooting.
• Interacts with and understands Empower, various data acquisition/management software for stand-alone laboratory systems, and LIMS
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.