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Senior Quality Assurance Representative

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Biopharma Careers
Full Time position
Listed on 2026-09-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Production QC/QA
Salary/Wage Range or Industry Benchmark: 69200 - 110900 USD Yearly USD 69200.00 110900.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

Work Location

Indianapolis, Indiana

Shift

No

Department

LS-SC-UYEQS1 QA Sterility Assurance

Recruiter

Katherine Hall

This information is for internals only. Please do not share outside of the organization.

Your Role

This role provides day shift support as quality assurance on-the-floor oversight for manufacturing activities at the facility.

Responsibilities
  • Reviews executed documentation to ensure steps are documented and verified at time of execution and that good documentation practices are being followed.
  • Performs and documents line clearances and room release for manufacturing use.
  • Reviews logbooks in manufacturing areas to ensure required activities are being completed and documented.
  • Monitors the formulation and filling processes to ensure cGMP compliance.
  • Provides aseptic core monitoring, acting as a SME for aseptic technique and providing reinforcement of aseptic practices to Manufacturing filling operators. Requires qualification in aseptic gowning and certification as an aseptic processing SME.
  • Observers, reports, and documents operator cleaning and disinfection practices.
  • Documents, reports, and trends observations stemming from Quality Oversight.
  • Documents and reports to management GMP violations, unsafe conditions, or other unusual results or practices.

Monday - Friday 10am - 6:30pm.

Physical Attributes
  • Lift and/or move up to 25 pounds.
  • Wear appropriate Personal Protective Equipment.
Minimum Qualifications
  • Bachelors Degree in Biology, Chemistry, or other Life Science Discipline and 2+ years of GMP pharmaceutical industry experience.
  • High School Diploma or GED and 5+ years of GMP pharmaceutical industry experience.
Preferred Qualifications
  • Experience with computer software applications including Microsoft Excel, Word, and Access.
  • Experience with Quality Management computer systems and SAP.
  • Experience with EU Annex 1 classified areas A, B, C, and D including acceptable aseptic behaviors, practices, and gowning.

Pay Range for this position: $69,200 - $110,900 / year

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses.

Benefits
  • health insurance
  • paid time off (PTO)
  • retirement contributions
  • other perquisites
Equal Employment Opportunity Statement

The Company is an Equal Employment Opportunity employer.

No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.

This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment.

Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately.

The Company will not retaliate against any individual because they made a good faith report of discrimination.

Position Requirements
10+ Years work experience
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