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Salary
$69k – $111k per year
Location
In office (Indianapolis, 10am - 7pm)
Seniority
Senior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 21, 2026. First seen by Alion on Sep 19, 2026. EMD Group scores B on the Alion truth index.

Overview
Company
Impact
Profile match
EMD Group is the name used in the United States and Canada by Merck KGaA, the science and technology group headquartered in Darmstadt, Germany, whose businesses cover healthcare, life science and electronics. Founded in 1668 and still majority-owned by the Merck family, the group operates in North America through EMD Serono, MilliporeSigma and EMD Electronics, with major sites in Burlington and Billerica in Massachusetts and Saint Louis in Missouri. Its board lists manufacturing technicians, process and quality engineers, data engineers and scientists, finance analysts and shared-service roles in Bengaluru, Manila and Tokyo.

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 include but are not limited to:

  • 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.

Who You Are:

Minimum Qualifications:

  • Bachelors Degree in Biology, Chemistry, or other Life Science Discipline and 2+ years of GMP pharmaceutical industry experience.

OR

  • 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 offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.

RSREMD

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.

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