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Chemistry Manager Jobs in Indiana (NOW HIRING)

... Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the ...

Secretary for Chemistry

Muncie, IN · On-site

$15 - $16.26/hr

... key management and distribution; submit service and maintenance-related requests when necessary; make room reservations as requested. * Assist with inquiries about the Chemistry graduate program ...

New

Secretary for Chemistry

Muncie, IN · On-site

$15 - $16.26/hr

... key management and distribution; submit service and maintenance-related requests when necessary; make room reservations as requested. * Assist with inquiries about the Chemistry graduate program ...

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Chemistry Manager information

What is the difference between Chemistry Manager vs Chemist?

AspectChemistry ManagerChemist
Required CredentialsBachelor's or Master's in Chemistry, often with management experienceBachelor's or Master's in Chemistry, sometimes with specialized certifications
Work EnvironmentLeads teams in laboratories or manufacturing facilities, oversees projectsConducts experiments, analyzes data, and develops chemical solutions
Employer & Industry UsageUsed in industries like pharmaceuticals, manufacturing, and R&D for leadership rolesCommon in research labs, quality control, and product development

The main difference between a Chemistry Manager and a Chemist lies in their responsibilities. Chemistry Managers oversee teams and projects, focusing on management and strategic planning, while Chemists primarily conduct experiments and analyze chemical data. Both roles require strong chemistry credentials, but the managerial position involves leadership skills and experience in supervising staff.

What is a chemistry manager?

Chemistry Managers are professionals who oversee the operations and staff within a chemistry laboratory or department. They are responsible for managing projects, ensuring compliance with safety and regulatory standards, supervising chemists and technicians, and maintaining lab equipment. Their role often involves coordinating research and development activities, budgeting, and implementing quality control procedures. Chemistry Managers play a vital role in ensuring that laboratory work is conducted efficiently and safely, often serving as a bridge between technical staff and upper management.

What are some common challenges faced by chemistry managers when leading a laboratory team?

Chemistry Managers often encounter challenges such as balancing administrative responsibilities with hands-on scientific oversight, ensuring strict compliance with safety and regulatory standards, and managing diverse teams of chemists and technicians. They also need to facilitate effective communication between team members and other departments, such as quality assurance or production. Addressing resource constraints and maintaining project timelines while fostering professional growth within their team are also typical aspects of the role.

What are the key skills and qualifications needed to thrive as a chemistry manager, and why are they important?

To thrive as a Chemistry Manager, you need an in-depth understanding of chemical processes, laboratory management, and a relevant degree in chemistry or chemical engineering, often supplemented by prior leadership experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as OSHA and EPA), and quality control protocols is typically required. Strong leadership, problem-solving, and effective communication skills help manage teams and collaborate across departments. These skills ensure safe, efficient laboratory operations and high-quality analytical results that support organizational goals.
What are the most commonly searched types of Chemistry jobs in Indiana? The most popular types of Chemistry jobs in Indiana are:
What cities in Indiana are hiring for Chemistry Manager jobs? Cities in Indiana with the most Chemistry Manager job openings:
Infographic showing various Chemistry Manager job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

QC Chemist, 3rd Shift

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Re-posted 9 days ago


Job description

Description
Quality Control Chemist Summary:
INCOG is seeking a Quality Control (QC) Chemist with a passion for working within a team, a desire to drive Quality processes in a regulated setting, and a commitment to upholding the integrity of data generated for clients.
The QC Chemist will work closely with the QC Chemistry Manager and Quality Control Method Transfer Scientists, as well as Project Management and Supply Chain teams, to support development, readiness, and routine testing activities for the Quality Control Chemistry laboratory.
This role is crucial in generating ALCOA+ data and upholding our Quality Mindset through attention to detail, on-time delivery, and commitment to Quality excellence. Strict adherence to Good Documentation Practices (GDP) is required as Good Manufacturing Practice (GMP) testing is performed.
Excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences is critical in this role. The QC Chemist will exemplify excellent interpersonal skills and be capable of developing productive, customer-centric working relationships with colleagues, clients, suppliers, and partners. The QC Chemist will thrive in a team environment but can also work autonomously with strong self-management and organizational skills.
Essential Job Functions:
  • Perform routine and batch-related testing on incoming components, raw materials, in-process samples, finished product, and stability samples according to validated methods as well as special testing deemed necessary by protocols
  • Assist in sampling and testing of incoming materials requiring QC testing as needed
  • Create/revise SOPs and other relevant documents related to laboratory equipment and/or processes
  • Participate in the completion of laboratory investigations/deviations and provide SME support where needed
  • Perform basic troubleshooting activities with respect to methods/assays, equipment malfunctions, and investigations (Deviations and OOS)
  • Execute routine laboratory work orders for maintenance and non-critical calibrations
  • Perform minor preventative maintenance on QC laboratory instrumentation as needed using written SOPs or assist vendors with access to systems/materials when vendor performs maintenance
  • Execute day-to-day tasks within the laboratory including sample inventory disposition/disposal, consumables ordering/inventory, preparing instruments for testing, and laboratory waste management
  • Assist in the control and management of laboratory waste in cooperation with relevant EH&S standards
  • Assist in the development and execution of protocols for method transfers, method validations, stability studies, cleaning validations, and any other special testing required from the Quality Control Chemistry laboratory
  • Support internal and external customers to ensure proper and timely execution of all aspects of the clinical/commercial analytical method life cycle across clients
  • Conduct periodic reviews of analytical test procedures and SOPs as required
  • Review and approve analytical testing procedures and protocols as needed
  • Assist in training fellow QC and Development personnel on instruments and assays when cross-training is needed
  • Assist in the professional support and development of QC Chemistry Technician staff within the QC laboratory
  • Be team-oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed
  • Set deadlines and prioritize work for self, group members, and support groups involved
  • Review/approve work performed by coworkers for accuracy and alignment with procedures
  • Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured, and released
  • Identify, evaluate, and implement continuous business process improvements

Special Job Requirements:
  • This position will support primarily third shift (11:00pm-7:30am)
  • Bachelor's Degree in Science (Chemistry or Biochemistry)
  • Minimum of 3+ years of biopharma industry experience, with at least 2 years of hands-on experience in a GMP environment/Quality Control testing in a regulated environment or other related experience
  • High proficiency level in operating UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC, particulate matter analyses, method validation/transfer, and relevant laboratory computer systems with associated data integrity requirements
  • Excellent working knowledge, understanding, and experience with practical implementation of FDA, EMA, and other regulatory authority expectations for Quality Control
  • Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.)

Additional Preferences:
  • Experience with Continuous Improvement, Six Sigma, and/or Lean principles
  • Experience with building processes and procedures
  • Experience in performing testing and/or characterization of biologic (monoclonal antibody, enzyme) and small molecule (peptide, mRNA) products
  • Experience performing container closure integrity testing (CCIT)

Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.