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Contract Gmp Manufacturing Jobs in Indiana (NOW HIRING)

Genovice

Validation Engineer (Contract)

Indianapolis, IN · Hybrid

$80K - $150K/hr

This is a contract role with strong potential for extension. Local candidates are preferred , but ... Author, review, and execute IQ/OQ/PQ protocols for a range of GMP manufacturing and laboratory ...

Intellectt INC

Deviation Writer

Indianapolis, IN · On-site

My name is Vyshu, and I'm reaching out from Intellectt Inc. regarding an exciting contract ... Strong understanding of GMP manufacturing processes and regulatory requirements. * Experience with ...

SpectronRx

Manufacturing Specialist

South Bend, IN · On-site

$28 - $35/hr

COMPANY OVERVIEW SpectronRx is a rapidly growing Contract Development and Manufacturing ... Performs chemistry manipulations for production in a GMP environment. * Ensure regulatory ...

SBM Management Services LP

GMP Manager

Lebanon, IN

$80K - $90K/yr

Maintain contract and contractor status databases * Review correspondence concerning contractors ... manufacturing, or service teams will also be considered. Certificates, Licenses, Registrations

SBM Management Services LP

GMP Manager

Lebanon, IN · On-site

$80K - $90K/yr

Maintain contract and contractor status databases * Review correspondence concerning contractors ... manufacturing, or service teams will also be considered. Certificates, Licenses, Registrations

Bristol-Myers Squibb Company

CMMS Coordinator

Indianapolis, IN · On-site

$17.25 - $23/hr

Act as a point of contact for contract service providers during on-site maintenance and calibration ... Support the maintenance of GMP manufacturing equipment and the management of spare parts inventory.

Bristol Myers Squibb

CMMS Coordinator

Indianapolis, IN · On-site

$17.25 - $23/hr

Act as a point of contact for contract service providers during on-site maintenance and calibration ... Support the maintenance of GMP manufacturing equipment and the management of spare parts inventory.

Novartis

Senior Automation Engineer

Indianapolis, IN

$124K - $186K/yr

... contracts and changes. • Responsible for the management, support and execution of automation ... GMP manufacturing operations including aseptic fill/finish and/or radio pharmacy is preferred. • ...

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Contract Gmp Manufacturing information

What are some common challenges faced in a Contract GMP Manufacturing role, and how can they be addressed?

Professionals in Contract GMP Manufacturing often face challenges such as adapting to diverse client requirements, ensuring strict regulatory compliance, and managing tight production timelines. Successful candidates should be comfortable working in fast-paced environments where priorities may shift quickly. Collaboration with cross-functional teams—like Quality Assurance, Regulatory Affairs, and clients—is essential to navigate these challenges. Maintaining clear communication and robust documentation practices helps ensure both compliance and client satisfaction.

What is Contract GMP Manufacturing?

Contract GMP (Good Manufacturing Practice) Manufacturing refers to outsourcing the production of pharmaceutical, biotechnology, or medical device products to specialized manufacturers who comply with GMP regulations. These contract manufacturers have the facilities, expertise, and quality systems required to ensure products are consistently produced and controlled according to regulatory standards. Companies often use contract GMP manufacturers to save costs, access specialized technology, or scale production quickly without investing in their own manufacturing infrastructure.

What are the key skills and qualifications needed to thrive as a Contract GMP Manufacturing professional?

Success in Contract GMP Manufacturing requires a solid background in bioprocessing or pharmaceutical manufacturing, a strong understanding of Good Manufacturing Practices (GMP), and typically a degree in a relevant scientific or engineering field. Familiarity with industry-standard quality management systems, batch record documentation, and equipment validation, as well as certifications like Six Sigma or cGMP training, are highly valued. Attention to detail, problem-solving skills, and effective communication help professionals navigate regulatory requirements and collaborate with clients and cross-functional teams. These competencies ensure product quality, regulatory compliance, and client satisfaction in a highly regulated manufacturing environment.

What is the difference between Contract Gmp Manufacturing vs Quality Control Analyst?

AspectContract Gmp ManufacturingQuality Control Analyst
CertificationsGMP training, relevant manufacturing certificationsGMP, QC certifications, lab skills
Work EnvironmentManufacturing facilities, production linesLaboratories, testing environments
Industry UsagePharmaceutical manufacturing, biotechQuality assurance, testing labs

Contract Gmp Manufacturing involves producing pharmaceutical products under GMP standards, focusing on manufacturing processes. Quality Control Analysts test and verify product quality in labs. While both roles require GMP knowledge, manufacturing roles emphasize production, whereas QC analysts focus on testing and quality assurance.

What are the most commonly searched types of Gmp Manufacturing jobs in Indiana? The most popular types of Gmp Manufacturing jobs in Indiana are:
What are popular job titles related to Contract Gmp Manufacturing jobs in Indiana? For Contract Gmp Manufacturing jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Contract Gmp Manufacturing jobs in Indiana look for? The top searched job categories for Contract Gmp Manufacturing jobs in Indiana are:
What cities in Indiana are hiring for Contract Gmp Manufacturing jobs? Cities in Indiana with the most Contract Gmp Manufacturing job openings:
Contract Gmp Manufacturing jobs near you
Infographic showing various Contract Gmp Manufacturing job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 4% Contract, and 3% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Deviation Writer/Technical Writer (Pharmaceutical)

Intellectt INC

Fishers, IN • On-site

Contractor

Re-posted 26 days ago

Job description

Hello,
 
I hope you’re doing well.
 
My name is Jayadev, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Deviation Writer/Technical Writer (Pharmaceutical)
based in Fishers, Indiana  with one of our prestigious clients.
 
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at  jayadev.g@intellectt.com
 

Position: Deviation Writer
Location: Fishers, IN

Job Summary

Seeking an experienced Deviation Writer to support GMP manufacturing operations by investigating deviations, non-conformances, and quality events. The role involves root cause analysis, CAPA development, technical writing, and collaboration with cross-functional teams.

Key Responsibilities

  • Write and investigate GMP deviations, non-conformances, and quality events.
  • Gather facts, review data, and determine root causes.
  • Perform Root Cause Analysis using 5 Why and Fishbone methodologies.
  • Develop and document CAPAs (Corrective and Preventive Actions).
  • Review historical deviations and identify trends.
  • Prepare clear and detailed investigation reports.
  • Collaborate with Manufacturing, Quality, Engineering, MS&T, and Supply Chain teams.
Required Qualifications
  • Bachelor's degree in Science, Engineering, or related field.
  • 4+ years of technical writing experience in a GMP-regulated environment.
  • Strong knowledge of GMP, deviation investigations, CAPA, and quality systems.
  • Experience with eQMS/EDMS systems.
  • Proficiency in Microsoft Word and Excel.
Must-Have Skills
  • Deviation Investigation Writing
  • GMP Manufacturing Experience
  • Root Cause Analysis (5 Why, Fishbone)
  • CAPA Development
  • Technical Writing
  • Pharmaceutical/Biotech Industry Experience
  • Quality Systems (eQMS, EDMS)
  • Cross-Functional Collaboration
    Thanks Regards,
    JAYADEV
    Sourcing Specialist
    Phone  (732)-997-6982   Ext: 308
    Email jayadev.g@intellectt.com