Fishers, Indiana, United States · On-site
$75k–$95k
Deviation Writer Summary INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our team. This role is crucial for translating a variety of complex technical events into clear, ac…
Skills: Technical Writing, Root Cause Analysis, GMP Compliance, Deviation Management, Ishikawa Fishbone
Fishers, Indiana, United States · On-site
INCOG BioPharma is seeking a highly motivated individual with subject matter expert (SME) capabilities in sterile pharmaceutical manufacturing process controls and industrial automation. The Equipment Specialist is a key…
Skills: Sterile Pharmaceutical Manufacturing, Industrial Automation, GMP Manufacturing, Aseptic Processing, Equipment Troubleshooting
Fishers, Indiana, United States · On-site
$113k–$132k/yr
Elevate is committed to providing the highest quality commercial roofing, wall and lining systems to solve our customers’ challenges, grounded by a 45-year legacy of proven experience. Our mission is to deliver solutions…
Skills: Spectroscopy, Chromatography, Rheology, Polymer Manufacturing, Data Analysis
Fishers, Indiana, United States · On-site
IN0534 Fishers, OH0523 Independence Bus Office, OH0713 NW Bancshares HQ, PA0258 Bellevue, PA0738 Processing Center Job Description The Core Application Developer II is a mid entry level systems application developer role…
Skills: RPGLE, SQL RPG, CLLE, Fiserv Signature, Fiserv Communicator
Fishers, Indiana, United States · On-site
$113k–$132k/yr
Elevate is committed to providing the highest quality commercial roofing, wall and lining systems to solve our customers’ challenges, grounded by a 45-year legacy of proven experience. Our mission is to deliver solutions…
Skills: Spectroscopy, Chromatography, Rheology, Data Analysis, SOP Authoring
Fishers, Indiana, United States · On-site
$100k–$120k
The Manufacturing Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor suppo…
Skills: Production Oversight, cGMP Compliance, Aseptic Techniques, People Leadership, Batch Planning
Fishers, Indiana, United States · On-site
$30/hr–$40/hr
Overview Commercial Service Electrician Fishers, IN | Full-Time Build Your Career with FSG Are you an experienced commercial electrician who enjoys troubleshooting, solving problems, and working independently? FSG is loo…
Skills: Commercial Electrical Troubleshooting, Electrical Repair, Preventative Maintenance, Blueprint Reading, Wiring Diagrams
Fishers, Indiana, United States · On-site
$100k–$120k
The Manufacturing Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor suppo…
Skills: Production Oversight, cGMP Compliance, Aseptic Techniques, People Leadership, Batch Planning
Fishers, Indiana, United States · On-site
$70k–$85k
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 int…
Skills: UHPLC/HPLC, GC, SoloVPE, UV-VIS, TOC
Allen County, Indiana, United States · Hybrid
$41k–$98k/yr
Be a part of our mission! As a world leader in creating comfortable, sustainable, and efficient climate solutions for buildings, homes and transportation, it's our responsibility to put the planet first. For us at Trane …
Skills: Customer Advocacy, Account Management, Inside Sales, Salesforce, Customer Retention
Fishers, Indiana, United States · On-site
Job ID: 14267 Alternate Locations: Newell Brands is a leading consumer products company with a portfolio of iconic brands like Graco®, Coleman®, Oster®, Rubbermaid®, Sharpie® and Yankee Candle® - and 24,000 talented team…
Skills: Lean Principles, Six Sigma, CAD, AutoCAD 3D, SAP
Fishers, Indiana, United States · On-site
$30/hr–$40/hr
Tom Wood Aviation, in Indianapolis, IN is searching for an Experienced A&P Technician to become a reliable member of our team at the Indianapolis Metropolitan Airport. The ideal candidate has a keen attention to detail, …
Skills: Aircraft Maintenance, Troubleshooting, Federal Aviation Regulations, Leadership, Supervisory Experience
Fishers, Indiana, United States · On-site
$34/hr–$40/hr
Benefits: Health insurance Paid time off 401(k) Dental insurance Employee discounts At Midas we are dedicated to providing quality services to customer vehicles in the areas of inspection, diagnosis and repair utilizing …
Skills: Vehicle Diagnostics, Tire Repair, HVAC Repair, Steering and Suspension, Brake Repair
Fishers, Indiana, United States · On-site
$34/hr–$40/hr
Benefits: Health insurance Paid time off 401(k) Dental insurance Employee discounts At Midas we are dedicated to providing quality services to customer vehicles in the areas of inspection, diagnosis and repair utilizing …
Skills: Vehicle Diagnostics, Tire Repair, HVAC Repair, Steering and Suspension, Brake Repair
Fishers, Indiana, United States · On-site
$21/hr–$28/hr
Job Summary The Quality Control Technician will be a member of the Quality Control Department. As a member of the team, he/she/they will be involved in routine QC sampling and testing of utilities, raw materials, in-proc…
Skills: QC Sampling, GMP, Analytical Chemistry, Sample Management, Equipment Calibration
Fishers, Indiana, United States · On-site
$21/hr–$28/hr
Job Summary The Quality Control Technician will be a member of the Quality Control Department. As a member of the team, he/she/they will be involved in routine QC sampling and testing of utilities, raw materials, in-proc…
Skills: QC Sampling, GMP, Analytical Chemistry, Sample Management, Equipment Calibration
Fishers, Indiana, United States · On-site
Job ID: 13890 Alternate Locations: Newell Brands is a leading consumer products company with a portfolio of iconic brands like Graco®, Coleman®, Oster®, Rubbermaid®, Sharpie® and Yankee Candle® - and 24,000 talented team…
Skills: Machine Repair, Mechanical Troubleshooting, Preventative Maintenance, Equipment Installation, LEAN Manufacturing
Fishers, Indiana, United States · On-site
MISSION To monitor and coordinate infrastructure projects and related costs and to execute the maintenance program for utilities and facilities, based on accurate and integrated plans, systems and tools for assigned site…
Skills: Infrastructure Management, Facilities Maintenance, Project Management, Budget Management, People Management
Fishers, Indiana, United States · On-site
$125k–$110k
Working closely with the QA Manager, the QA Batch Supervisor will be instrumental in supporting major QA programs. They will also be key in championing and developing the organization’s Quality Mindset, and culture of ef…
Skills: Batch Record Review, Aseptic Processing, Quality Management Systems, Root Cause Analysis, CAPA
Fishers, Indiana, United States · On-site
$125k–$145k
Manager of Device Assembly & Packaging Summary The Manager of Device Assembly & Packaging holds strategic and operational accountability for INCOG's device assembly and packaging (DAP) program, overseeing 24/7 DAP operat…
Skills: cGMP Compliance, Device Assembly, Packaging Validation, Lean Six Sigma, Regulatory Readiness
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The Deviation Writer is responsible for investigating and authoring technical reports on nonconforming events to identify root causes. They collaborate with cross-functional teams to implement effective corrective and preventative actions to prevent future occurrences.
Candidates must have a bachelor's degree in a scientific or engineering discipline and at least 3 years of technical writing experience in a regulated GMP environment. Proficiency in analysis tools and electronic document management systems is highly preferred.
INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The Deviation Writer will work closely with the Manufacturing, Production Engineering, Manufacturing Sciences and Technology, Supply Chain, Quality, and other cross-functional teams to create comprehensive investigations that leverage facts and data to support robust root cause conclusions, effective corrective actions, and systematic all-encompassing preventative actions. The Deviation Writer will exemplify excellent interpersonal skills and be capable of developing productive customer-centric working relationships with internal and external customers and have a role with high visibility to all departments. The Deviation Writer will have strong familiarity with industry standard electronic Quality Management System(s) and Microsoft Office suite products.
They will thrive working autonomously utilizing strong self-management and organization skills but also be able to interact, collaborate, and lead within a team environment. The Deviation Writer will value the processes owned by internal customers and subject matter experts and will possess a demonstrated ability to support and influence positive outcomes in the application of that knowledge to wider processes.
· Understand, investigate, and author a variety of deviating conditions or nonconforming events across multiple technical departments, in alignment with Subject Matter Experts.
· Self-motivated to fact gather, analyze information, interpret data, utilize expertise from Subject Matter Experts, etc. in an effort to provide supportive evidence to the investigation and root cause.
· Experience utilizing a variety of analysis tools to support root cause identification; Ishikawa Fishbone, 5 Why, etc.
· Ability to critically think outside the box for robust corrective and preventative actions; leveraging automation and engineering controls to error-proof equipment and processes.
· Demonstrated ability to translate complex, technical processes and descriptions into simplified, understandable write ups.
· Eagerness to collaborate and partner with both internal and external stakeholders to comprehensively represent the facts of an investigation in a logical and presentable manner.
· Evaluating historical deviating conditions, adverse events, non-conformances, etc. in order to identify and prevent trends.
· Bachelor’s degree in a scientific, engineering, or technical discipline.
· Minimum of 3 years of experience in technical writing within a regulated GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries.
· Proficient in writing clear, concise, and accurate technical documentation.
· Strong understanding of GMP manufacturing processes and regulatory requirements.
· Excellent organizational skills with high attention to detail.
· Ability to collaborate effectively with cross-functional teams and communicate complex information to diverse audiences.
· Familiarity with documentation tools and electronic document management systems (EDMS).
· Exceptional computer skills, particularly moderate to expert level experience with Microsoft Word and Microsoft Excel.
· Ability to manage multiple projects and deadlines simultaneously.
· Paid vacation days, amount based on tenure, and paid sick time
· 11 observed holidays
· 401(k) plan with company match up to 3.5% of salary, vested immediately
· Choice of health & wellness plans
· FSA and HSA programs
· Dental & vision care
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.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
A CDMO with an unparalleled customer-centric approach.
Our services support injectable drug products, including technical transfer, analytical method development and validation, process scale up, and formulation & filling of vials, syringes and cartridges. In addition, we offer customized packaging services to include labeling, device assembly, auto injector assembly, cartoning, final packaging and integrated storage solutions at various temperature conditions.
Offices: Fishers , Indiana, US
There are currently 82 open engineering positions in Fishers, IN listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include INCOG BioPharma Services, Thermo King, Amrize, DCCM, Facility Solutions Group, among others. Browse the listings above to see every active employer.
Yes — 6 of the 82 open engineering positions offer remote or hybrid work (2 remote, 4 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
