QC Analytical - Group Leader

Lab Responsibilities:
Perform routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory
Utilize laboratory instruments and equipment in accordance with established procedures to include but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC and conductivity, and various other instruments
Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.)
Leadership Responsibilities:
Act as a technical resource, trainer, and troubleshooter for the department
Make recommendations for operational and/or technical improvements
Communicate effectively within the group
Coach and develop direct reports
Plan and monitor workflows
Monitor and approve employees’ time worked through time-entry system
Support and promote company policies and procedures
The site is not accessible by public transportation routes/options.
BS in Chemistry or Biochemistry with a minimum of 2 years of experience working in a laboratory environment, QC laboratory preferred.
Experience working with analytical standards, reagents, and laboratory instruments
Successful hands-on analytical testing experience in a Good Manufacturing Practices {also cGMP} environment
Understanding and performing analytical testing and the use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity
Capability to perform complex mathematical problems and perform complex data analysis
Accurate pipetting skills
Previous leadership experience preferred
Authorization to work in the United States indefinitely without restrictions

Employment type
Full-time

Work arrangement
No