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Chemist- QC

BioSpace

Indianapolis (IN)

On-site

USD 63,000 - 163,000

Full time

5 days ago
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Job summary

A leading healthcare company seeks a Chemist for their QC role in Indianapolis. This position involves testing laboratory samples, ensuring compliance with safety standards, and supporting quality system improvements. Ideal candidates will have a Bachelor's in Chemistry or Biology and relevant GMP lab experience. The role includes training others and sharing best practices in a collaborative environment.

Qualifications

  • Relevant GMP lab experience preferred.
  • Proficiency with computer systems required.
  • Ability to work safely in a lab environment.

Responsibilities

  • Verify analytical data of other analysts.
  • Perform analytical tests following procedures.
  • Participate in investigations and troubleshooting.

Skills

Analytical skills
Communication
Interpersonal skills

Education

Bachelor's degree in Chemistry, Biology, or related Science

Tools

Microsoft Office
LIMS

Job description

Join to apply for the Chemist- QC role at BioSpace.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work to discover and bring medicines to those in need, improve disease management, and support communities through philanthropy and volunteerism. We prioritize people and strive to make a difference worldwide.

Position Overview

The Chemist in the B105 DC In-Process Laboratory performs accurate testing of routine and some non-routine lab samples following GMP and safety guidelines. Responsibilities include verification of results, participation in root cause investigations, equipment evaluations, and quality system improvements. The role involves sharing technical information and best practices within the plant or group.

Key Responsibilities
  • Verify analytical data of other analysts in the lab.
  • Perform analytical tests safely and accurately according to procedures.
  • Review data for accuracy and conformance.
  • Participate in investigations of deviations and equipment troubleshooting.
  • Assist in improving quality systems and documentation.
  • Share technical knowledge and best practices.
  • Write protocols for non-routine testing and validation.
  • Ensure compliance with safety standards.
  • Train and mentor others, developing training materials.
Preferred Qualifications
  • Maintain a safe work environment and support HSE goals.
  • Proficiency with computer systems, including Microsoft Office and LIMS.
  • Ability to work in a lab environment with appropriate PPE.
  • Strong math, documentation, communication, and interpersonal skills.
Educational Requirements
  • Bachelor's degree in Chemistry, Biology, or related Science field with relevant GMP lab experience.
Additional Information
  • Work schedule: 4-10 hour night shifts with rotating weekends.
  • May require off-shift communication via company phone.
  • Minimal travel; exposure to allergens in the plant.
  • Repetitive tasks may be involved; post-offer testing may be required.

Lilly is committed to diversity and inclusion. Accommodations are available for applicants with disabilities. We are an Equal Opportunity Employer. Compensation ranges from $63,000 to $162,800, depending on experience and location, with additional benefits and bonuses.

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