Jobs in Indianapolis, IN

Neurology Physician Job near Indianapolis, IN Looking for a BC/BE neurologist to join a hospital-employed practice.

We offer all the advantages of a single hospital community, low managed care environment, a large referral base with immediate practice load, and supportive medical staff.

The call is 1:4.

This position offers Full Hospital Benefits, Competitive Salary, Sign on bonus, and Student Loan Repayment.

If you are interested in hearing more about this opportunity, please call or text HDA MD Staff at .

You can also reach us through email at .

Please reference Job ID j-19378.

Wetland Scientist

Indianapolis, IN

Direct Hire

Overview

Client is seeking an experienced Wetland Scientist to lead wetland and stream assessment work from our Indianapolis office. This role provides the opportunity to support environmental compliance efforts, lead field investigations, and contribute to infrastructure and transportation projects throughout Indiana.

What You’ll Do

· Lead and direct wetland and stream delineation fieldwork and reporting

· Conduct wetland delineations, stream assessments, and floristic inventories

· Support preparation of Clean Water Act (CWA) Section 401/404 permit applications

· Assist with mitigation monitoring and habitat assessments

· Collaborate with project teams and agencies to support environmental compliance

What We’re Looking For

· 7 to 10 years of experience in wetland delineations, stream assessments, and related environmental work

· Strong understanding of wetland and stream regulations and permitting processes

· Experience with floristic inventories and habitat assessments

· PWS (Professional Wetland Scientist) certification preferred

· Previous experience with INDOT projects preferred but not required

Work Environment & Flexibility

This position offers a flexible work environment that may include a combination of office-based work, field work, and remote flexibility. Occasional travel may be required for inspections, site visits, and coordination meetings.

Compensation & Benefits

Competitive salary based on experience. RGI offers a comprehensive benefits package including health, dental, and vision insurance, health savings account (HSA), retirement plan with company match, paid time off, holidays, and professional development support.

• Higher Weekly pay
• Better Home Time
• Manual Transmission Trucks
• Very Nice Equipment
• Great Benefits, including Medical, Dental and Vision

• Medical Bridge (First 60 days of Employment)
• Major Medical (Starts after 60days of Employment)
• Dental (Starts after 60days of Employment)
• Vision (Starts after 60days of Employment)
• Life Insurance and 401K (Starts after 60days of Employment)
• All employees must enroll in benefits within 60 days of hire
• All benefits provide Nationwide coverage

• 21 years or older
• CDL A, 6 Months of Experience
• Qualified applicants with arrest and conviction records will be considered for employment pursuant to applicable federal, state, and local laws.

Production Control Planner - Specialist

(Scheduler / Planner Function)

The Production Planning & Scheduling specialist will join a 500 person, Global Manufacturing company to focus on planning and scheduling assembly lines, monitoring Customer Orders & due dates (as well as inventory) and coordinate / plan with production teams to ensure that the right parts get built at the right time.

Work will involve, Planning, Scheduling, Checking Inventory, Using the ERP / MRP system....and working in close concert with Production teams to ensure that products can be built on time.

Skills / Requirements

• 7+ years experience as either Planner or Scheduler or / in Production Planning, Production Control planning, Materials Management.
• Experience gained in Manufacturing Environment working in planning or scheduling or production control with use of ERP or MRP systems.
• Professional attributes - Communicate well, good interpersonal skills to deals tie others effectively .

FPC - FORTUNE PERSONNEL CONSULTANTS (Orlando Office):

For additional information, visit us on the web at or contact Maria Aviles on 4 Ext 133 --> Please apply for position before you call.

*We are looking for local candidates who presently reside in Central Indiana

Keywords - Materials Manager, Production Control Manager, Planner, Scheduler, Planning, Scheduling, Supply Chain Management, Inventory Management, Master Scheduler, Planning, Automotive, Electronics Manufacturing, Electrical Manufacturing, Production, Planner, Planning, college graduate, planner, scheduler, plan, Production control

At 500 Republic, our sales team is made up of highly skilled and experienced sales professionals who are passionate about what they do. We specialize in face-to-face interaction with our customers, and our expertise in this area has enabled us to acquire more customers than internal sales teams can. We work closely with our clients to develop tailored sales strategies that are designed to meet their unique needs and goals.

What you'll be doing as an Entry Level Account Manager:

• Oversee sales accounts in your territory.

• Build relationships with your customers.

• Deliver sales presentations.

• We provide the training to teach/train you everything you will need to be successful at 500 Republic

Requirements of the Entry Level Account Manager:

• Outstanding people skills

• Excellent customer-facing and communication skills

• Competitive spirit

• Team player

• BS/BA degree is preferred

What we offer every Entry Level Account Manager:

• Competitive pay structure

• Training and development

• Access to industry leaders

• Holidays off

• Constant support from the management team

• Team environment

• Paid training

Job Title: Production Technician

Work Address: 6925 Guion Rd, Indianapolis

Pay Rate: $30 - 33/HR

Shift: 7 am - 7:30 pm = 2 days on 2 days off and every other weekend.

Interviews: Onsite Preferred; Virtual okay

Position Overview:

This is a senior-level position in the bulk processing area. The employee will utilize experience and training to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through several job functions and be required to demonstrate increasing skill levels.

Major Position Activities & Responsibilities:

• HS or Equivalent

• 5+ years’ experience in a production environment (chemical/pharmaceutical/biochemical).

• GMP, GDP, of 5 years or more. A bachelor's degree in pharmaceuticals or chemistry is preferred.

• SAP knowledge a plus

• Learn, understand, and comply with all Company and GMP compliance policies/procedures.

• Learn and perform area sanitization procedures in a GMP Manufacturing facility (Formulation Rooms,

Staging Areas, Raw Material Dispensing Room, and Airlocks).

• Learn and become competent in performing filter integrity testing.

• Learn and become competent in cleaning miscellaneous pieces of manufacturing equipment and

vessels.

• Learn and perform raw material weighing (dispensing) and bulk formulation.

• Perform system maintenance PM’s / procedures.

• Become and maintain qualification for entry into the Aseptic Core in order to perform sterile filtrations,

unload the autoclave, and complete Steam-in-Place operations as deemed necessary by area

management.

• Perform other duties supporting the production schedule as assigned by area supervision.

• Execute tasks/operations with minimal supervision.

• Provide training/guidance/leadership for Production Technician I and II personnel.

• Supervise the activities of other members of the manufacturing team, taking full responsibility for

results.

• Coordinate manufacturing activities with other support groups to receive components, batch records,

QC results, etc.

• Conduct QTS nonconforming product investigations, identify corrective actions, and implement

changes as needed.

• Place purchase orders and monitor supplies.

• Perform final batch record reviews before QA review.

• Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in that

training by passing test(s) administered by the company or consultant providing such training.

• Performs special projects and other duties as assigned.

• As a part of the employee’s job requirements, the employee may be required to handle wastes

including hazardous wastes. The employee must attend mandatory annual hazardous waste training

meeting(s) and show competency in that training by passing test(s) administered by the company or consultant providing such training.

• Must immediately notify supervisor if affected by infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist.

Scope:

• This position has no direct reports.

Background Qualifications:

• High school diploma or the equivalent. B.S. degree in chemistry/biology/life sciences is a plus.

• Minimum of five years of experience using current Good Manufacturing Practices (GMP) in a regulated manufacturing facility pharmaceutical/biotech/diagnostic industry) with Processing experience.

• Adequate communication skills to read, comprehend, and discuss detailed GMP documentation (batch record instructions, Standard Operating Procedures, etc.).

• Extensive knowledge of and experience in bulk formulation along with equipment cleaning, preparation, and assembly are preferred.

• As persons in this role are engaged in the open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body.

• Strong attention to detail.

• Ability to perform arithmetic functions to accurately perform or check calculations required in manufacturing instructions.

• Leadership experience in training/directing others.

• Strong mechanical aptitude.

• Ability to troubleshoot, identify problems, and propose solutions.

• While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand. The employee is occasionally required to sit; walk; stoop, kneel, bend, crouch, crawl, talk or hear.

The employee must regularly lift and /or move up to 10 pounds, and frequently lift and/or move up to 25 pounds.

• Specific vision abilities required by this job include close vision, distance vision, color vision, and peripheral vision.

• Computer skills in Microsoft Office such as Word and Excel are a plus

Trident Consulting is seeking a " Production Technician (Aseptic/Pharmaceutical)" for one of our clients. A global leader in business and technology services.

Job Title: Production Technician (Aseptic/Pharmaceutical)

Location: Indianapolis, IN 46268, USA

Category: Supply Chain

Labor Type: Industrial

Pay Rate: $30–$33/hr on w2

Duration: 03/09/2026 to 03/08/2027

Type: Contract

Job Description

The role supports aseptic pharmaceutical manufacturing operations, requiring significant training and demonstrated expertise. Responsibilities include:

Operations & Equipment

1. Set up, calibrate, and operate equipment according to specifications
2. Adjust filler and labeler equipment with proper parts/settings
3. Assemble containers and components for portioning
4. Portion materials into containers safely
5. Set up, operate, and troubleshoot automated labeling and bagging equipment
6. Conduct housekeeping, disinfection, and autoclaving as required
7. Maintain accurate records of tests, measurements, calibrations, and conversions
8. Monitor inventory and stock necessary supplies

Compliance & Safety

1. Wear appropriate PPE (steel-toed shoes, other safety equipment)
2. Follow FMP, SOPs, UOPs, and safety rules
3. Maintain cleanliness of equipment and work areas
4. Report safety or quality concerns immediately
5. Maintain certification for entry into the Aseptic Core
6. Independently make important decisions during processing
7. Oversee work of other Manufacturing team members

Process Improvement

1. Suggest improvements to save cost or improve efficiency
2. Participate in testing and implementation of changes

Qualifications

1. Education: High School Diploma, GED, or HSED required; college coursework in chemistry desirable
2. Experience:
3. Minimum 2 years in pharmaceutical aseptic manufacturing (food industry aseptic experience not accepted)
4. Experience in Clean Room/Aseptic environments, Equipment Preparation, Stopper Preparation, Semi-automated/manual Inspection, Packaging Operations, Sanitization, Autoclave operation
5. Skills & Knowledge:
6. Basic math including metrics/conversions
7. Mechanical aptitude and eye-hand coordination
8. Ability to use hand/air tools, pumps, electronic scales, and material handling equipment
9. Strong communication, teamwork, problem-solving, and documentation skills
10. Ability to train others

About Trident:

Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology and engineering professionals in contract and full-time roles. Trident's commitment is to deliver the best and brightest individuals in the industry for our clients' toughest requirements.

Some of our recent awards include

• 2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America
• 2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area

Hiring: Production Technician in Indianapolis, IN

Title: Production Technician/ Manufacturing Technician

Location: Indianapolis, IN 46268

Shift: 7:00 AM – 7:30 PM (2 days on / 2 days off + every other weekend)

Interviews: Onsite preferred (virtual available)

Pay: $30–$33/hr

Overview:

We are seeking an experienced Production Technician III to join a pharmaceutical manufacturing team in a GMP-regulated environment.

Responsibilities:

• Perform bulk formulation, raw material dispensing, and equipment cleaning
• Execute GMP-compliant manufacturing processes and documentation
• Conduct filter integrity testing and sterile filtration activities
• Support aseptic operations (autoclave, SIP, cleanroom entry)
• Coordinate with QA, QC, and supply teams
• High School Diploma (Bachelor’s in Chemistry/Biology preferred)
• 5+ years in pharmaceutical/biotech/chemical manufacturing
• SAP and MS Office knowledge (preferred)

If you are interested, email your resume to

Trident Consulting is a premier IT staffing firm providing high-impact workforce solutions to Fortune 500 and mid-market clients. Since 2005, we've specialized in sourcing elite technology and engineering talent for contract, direct hire, and managed services roles. Our expertise spans cloud, AI/ML, cybersecurity, and data analytics, supported by a 3M+ candidate database and a 78% fill ratio. With a highly engaged leadership team and a reputation for delivering hard-to-fill, niche talent, we help organizations build agile, high-performing teams that drive innovation and business success. Learn more: .

Some of our recent awards include:

• Ranked as the #1 Women Owned Business Enterprise in the large category by ITServe.
• Received the TechServe Excellence award.
• Consistently ranked in the Inc. 5000 list of fastest-growing private companies in America.

#ProductionTechnician #ManufacturingJobs #PharmaJobs #BiotechJobs #ChemicalIndustry #LifeSciencesJobs #GMP #GoodManufacturingPractices #AsepticProcessing #SterileManufacturing #BulkProcessing #CleanroomJobs #PharmaceuticalManufacturing

Overview:

We’re hiring a Project Scheduler to join a pharmaceutical manufacturing organization in Indianapolis, Indiana. This full-time, on-site role is ideal for an experienced scheduler with a strong background in capital projects and regulated manufacturing environments.

Key Responsibilities:

• Manage workload and set priorities for small team of schedulers.
• Ensure consistency of design, level of development and quality for schedules for the team
• Develop, maintain, and manage integrated project schedules (Level 1 – 4) using Primavera P6.
• Track progress, identify schedule risks, and support mitigation planning.
• Generate schedule metrics and reporting by integrating Primavera P6 and Excel data.
• Communicate schedule status, milestones, and critical path updates to project stakeholders.

Qualifications:

• Bachelor’s degree in Engineering, Manufacturing, Project Management, Operations, or project support experience in a related field.
• Prefer a mix of capital project planning, design, delivery and start-up experience and schedule development in Primavera P6.
• Where project delivery and scheduling experience are not available,
• Proven ability (> 2 years) to develop, project schedules using Primavera P6 or other modern scheduling tools (i.e., Smartsheets, MS Project, etc.)

Or -

• Desire to master the scheduling discipline combined with demonstrated project delivery experience (> 5 years) across all phases of work in a regulated industry (planning, design, procurement, construction, commissioning, qualification.
• Strong problem-solving skills and ability to multitask and prioritize in fast-paced environments.
• Excellent verbal and written communication skills.

About Our Culture:

At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.

Learn more about us:

Visit our website at to explore our projects, expertise, and the impact we make in the engineering and consultancy space.

Process Alliance is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.

Job Title: Data/Software Engineer

Location: Remote

Industry: Pharmaceutical

***NO C2C***

Job Description:

Theoris Services is assisting our client in their search for a Data/Software Engineer to add to their growing team. Our client is seeking someone with data visualization experience and software engineering (create reusable libraries, best practices, troubleshooting).

Responsibilities:

• Data Pipeline & Backend Development
• Design, build, and optimize scalable data pipelines and ETL/ELT processes to integrate and harmonize scientific data (compounds, assays, experiments) from 30+ heterogeneous sources.
• Implement and maintain lakehouse architectures on AWS (S3, Glue, Athena, Iceberg) to support multibillion-record datasets.
• Develop federated query capabilities using Trino (or similar distributed engines) for unified access across platforms like PostgreSQL, Snowflake, and others.
• Build robust backend services, RESTful APIs, and data services using Python (FastAPI, Flask preferred) to enable seamless data flow and integration with scientific tools (e.g., Benchling, computational chemistry systems, AI/ML endpoints).
• Performance Optimization & Troubleshooting
• Optimize query and database performance for complex analytical workloads across PostgreSQL, Iceberg, Trino, and other platforms.
• Implement caching, indexing, and query tuning techniques to improve response times and scalability as data volumes and user bases grow.
• Apply reverse engineering and advanced troubleshooting skills to debug complex data issues, pipeline bottlenecks, application failures, and performance problems proactively.
• Monitor systems, identify root causes, and implement fixes for data and application reliability.
• Data Visualization & User-Facing Analytics
• Design and develop interactive dashboards, visual analytics, and scientific data visualizations using Power BI and Spotfire (or equivalent tools).
• Create reusable visualization components and data-rich UIs (React/TypeScript preferred) to enable scientists to search, filter, explore, and interpret complex datasets—including dose-response curves, chemical structures, and analytical results.
• Translate scientific and engineering data into clear, actionable visual insights for researchers and stakeholders.
• Software Engineering & Quality Practices
• Apply best software engineering practices: modular/reusable design, clean code principles, code reviews, comprehensive documentation, and creation of maintainable libraries/services.
• Write high-quality unit, integration, and end-to-end tests; use mock data effectively to create reliable automated test cases and ensure code stability.
• Implement CI/CD pipelines for automated testing, deployment, and monitoring on AWS (EC2, ECS, Lambda, S3).
• Collaborate on full-stack features from database to frontend, ensuring end-to-end functionality, security (SSO/LDAP), and performance.
• Collaboration & Governance
• Partner with scientists, UX designers, and cross-functional teams to gather requirements, conduct user testing, and iterate on usability.
• Implement data validation, quality checks, metadata management, and governance to ensure compliance and accuracy.
• Contribute to engineering best practices and foster a culture of quality and scalability.

Requirements:

• Education & Experience
• Bachelor's degree in Computer Science, Data Engineering, Software Engineering, Information Systems, or a related technical field.
• 3+ years of professional experience in data engineering, full-stack development, or closely related roles.
• Proven track record of building and delivering production-grade data pipelines, platforms, and/or user-facing scientific applications.
• Technical Skills
• Programming: Intermediate to strong proficiency in Python (core for pipelines, backend, and data manipulation with pandas/PySpark); familiarity with JavaScript/TypeScript for frontend.
• Data Engineering: Hands-on experience creating scalable pipelines, ETL/ELT processes, and distributed processing (Spark, Trino/Presto).
• Databases & Querying: Deep expertise in relational databases (PostgreSQL), modern warehouses (Snowflake, Redshift), and query engines; strong focus on query performance improvement and optimization.
• Cloud Platforms: Practical experience with AWS services (S3, Glue, Athena, Lambda, RDS, EC2/ECS).
• Data Visualization: Proven experience with Power BI and Spotfire (or similar) for scientific and analytical dashboards/visualizations.
• Frontend (preferred): Modern JavaScript/TypeScript frameworks (React preferred), responsive UI development, and component libraries.
• Testing & Quality: Strong unit testing skills; experience writing automated tests with mock data for robust coverage.
• Tools & Practices: Git for version control; API design (RESTful); CI/CD; clean code and reusable library development.
• Core Competencies
• Excellent reverse engineering and troubleshooting capabilities for complex data and system issues.
• Strong problem-solving skills with attention to detail and commitment to data quality/accuracy.
• Ability to work independently and collaboratively in cross-functional, scientific teams.
• Excellent communication skills to bridge technical concepts with non-technical stakeholders (scientists, researchers).

Best-In-Class-Benefits:

We are in the people business; treating people right is our ONLY priority. Theoris Services consultants are full-time employees with full benefits, including:

• Robust Health Insurance
• 401(k) plan

About Theoris:

Our goal is to Fuel Your Career! As a Theoris team member, you join a culture based on people-centered values and an environment that fosters both personal and professional growth. We build long-term relationships with our clients and our consultants. With over 30 years of building strong relationships in the industry, we’re uniquely positioned to make the right connections. This knowledge is used to find the right job placement. Our recruiting teams are experts dedicated to the information technology and engineering staffing space and are highly respected by our client base.