486 Quantigen Biosciences jobs in Indianapolis,IN

Formulation Associate Scientist Entry Level

Pace Analytical Life Sciences

Indianapolis, IN 46227

$23-$25/hr

OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline
0–2 years of relevant experience (including internships or undergraduate research) in a laboratory setting, preferably involving biologics or biopharmaceutical products
Hands-on experience working with standard laboratory equipment
Shift: Monday through Friday, 8:00AM - 5:00PM
Compensation: $23.00 - 25.00/hr

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Microbiologist

United States Army

Indianapolis, IN 46227

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Associate Director - Technical Services/Manufacturing Science (TSMS) - API External Manufacturing (Peptides)

Lilly

Indianapolis, IN 46262

OnsiteHealth InsurancePaid Time OffRetirement Benefit

B.S. in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline
8+ years of relevant experience in manufacturing within the pharmaceutical or biotechnology industry
Proven leadership experience, including direct supervision and mentorship of scientific and technical staff.

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Scientist 1

Pace Analytical Services

Indianapolis, IN 46227

$20/hr

OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in Chemistry, Biochemistry, or other STEM related degrees — or an equivalent combination of education, training, and experience
Ability to work effectively in a laboratory environment, including standing for extended periods, working around strong odors, and wearing required PPE (lab coat, safety glasses, gloves—all provided by Pace®)

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Senior Quality Assurance Representative

Merck Group

Indianapolis, IN 46227

$69,200-$110,900/yr

OnsiteHealth InsurancePaid Time OffRetirement Benefit

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.
This role provides day shift support as quality assurance on-the-floor oversight for manufacturing activities at the facility.
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.
Lift and/or move up to 25 pounds.
Wear appropriate Personal Protective Equipment.
The role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

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Advisor - Technical Lead Scientist - Advanced Therapies Manufacturing

Lilly

Lebanon, IN 46052

~ 33 min OnsiteHealth InsurancePaid Time OffRetirement Benefit

B.S. in Biotechnology, Biochemistry or related quantitative field
3+ years of experience in pharmaceutical/biotech manufacturing industry
1+ year of experience with new product submission and filing

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Active Entomologist

United States Army

Indianapolis, IN 46227

New, Posted 13 hours ago

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Area Manager II

Amazon.com Services LLC

Greenwood, IN 46142

~ 33 min OnsiteFlexible ScheduleHealth InsurancePaid Time OffRetirement Benefit

2+ years of employee and performance management experience
Bachelor's degree or equivalent, or 2+ years of Amazon (blue badge/FTE) experience
Work a flexible schedule/shift/work area, including weekends, nights, and/or holidays
Lift up to 49 pounds and frequently push, pull, squat, bend, and reach
Stand/walk for up to 12 hours during shifts
Work in an environment where the noise level varies and can be loud
Work in an environment that is subject to variable temperatures and weather (delivery stations include outside loading departments)
Continuously climb and descend stairs (applies to sites with stairs)

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Pharmaceutical Project Manager

Johnson Controls

Indianapolis, IN 46262

OnsiteHealth InsurancePaid Time OffRetirement Benefit

Bachelor's degree in construction, Civil, Mechanical, Electrical Engineering, Construction Management, Business Management, Architecture, or a related field.
5–10 years of direct project management experience on large capital projects, including regulated or validated settings (typical project sizes in the $5–$20M range; portfolio responsibility not required).
Demonstrated success delivering complex, multi-site projects in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
Understanding of contract language, project accounting, and basic portfolio management as they apply to validated environments.
Strong executive communication skills; ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
Ability to lead and coordinate cross-functional teams (Owners, Architects, Engineers, QA/Validation, Contractors) in regulated contexts.
Proficiency with standard project management tools (Primavera P6, MS Project) and reporting platforms; advanced skills in MS Office with the ability to create executive-level dashboards and presentations.
Working knowledge of validation concepts, commissioning/qualification processes, data integrity best practices, and regulatory expectations for validated facilities.
Ability to establish and maintain professional relationships with key stakeholders and subcontractors in validated environments.
Willingness to travel and operate across multiple sites as needed.

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