QC Supervisor (3rd Shift)

Lead Candidate; Fishers (IN); On-site; USD 70,000 - 85,000; Full time

Job summary

A biopharma company located in Fishers, Indiana is seeking a QC Supervisor for their 3rd Shift (11pm to 7:30am). This role involves providing technical support and team leadership in Quality Control for Chemistry and Microbiology. The ideal candidate should have 3-5 years of GMP laboratory experience, a relevant Bachelor's degree, and some leadership background. Strong expertise in laboratory instrumentation is advantageous. This position offers the chance to influence team goals and values, promoting an inclusive workplace.

Qualifications

• 3-5 years of experience in GMP laboratory operations.
• Experience in using various laboratory instruments for analysis.
• 1-2 years of leadership experience.

Responsibilities

• Provide technical support and team leadership for QC.
• Assist in team member development and performance communication.
• Develop and improve QC processes.

Skills

GMP laboratory operations

Laboratory instrumentation

People leadership

Education

Relevant Bachelor’s degree

Tools

pH/conductivity meters

UHPLC/HPLC systems

GC/CE instruments

Job description

Overview

INCOG Biopharma Services in Indianapolis, IN is hiring a QC Supervisor to cover their 3rd Shift (11pm to 7:30am) who will report to the QC lab leadership (Chem/Micro). They will be involved in QC deviation investigations, laboratory investigations and CAPA implementation. They will also influence the accomplishments of companywide and team goals and objectives as well as inspire team members while consistently modelling ALP values in all interactions.

Responsibilities

• Provide technical support, oversite and team leadership for Quality Control Chemistry, Microbiology and Quality Control Technical Services.
• Assist in the development of individual team members by providing mentorship to analysts/data reviewers and communicating with Quality Control Leadership on team performance.
• Develop and improve current processes to maintain and control the general functions of INCOG Quality Control.

Qualifications

Ideally, candidates will have 3-5 years working knowledge of GMP laboratory operations (Chemistry or Microbiology), as well as a relevant Bachelor’s degree. They will also have:

• Experience with using laboratory instrumentation from pH/conductivity meters, osmometers, and density meters to more complicated systems used for UHPLC/HPLC, GC, CE, icIEF, endotoxin, and bioburden analysis.
• 1-2 years of people leadership experience

Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself…

Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.