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Contract Gmp Manufacturing Jobs in Indiana (NOW HIRING)

BEPC INC

Be Seen First

Production Technician - 30346_PC

Indianapolis, IN · On-site

$27 - $30/hr

Working knowledge of GMP compliance requirements and controlled pharmaceutical manufacturing ... Contract Details * Employment: Temp-to-Perm * Schedule: Monday-Friday, 7:00 AM-3:30 PM * Shift: 1st ...

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

Direct the development and establishment of processes in GMP. Accountable for developing a scalable ... Contract Development and Manufacturing Organizations Experience with cell culture technologies ...

Anveta

Senior CSA CTOP Coordinator

Lebanon, IN · On-site

Lebanon, IN 100% on site Contract Length: 2+ Years 8+ years CTOP experience, some pharma required ... Ensure turnover packages meet GMP, FDA, and project-specific quality requirements * Identify risks ...

Cynet Systems

Training Associate

Indianapolis, IN · On-site

$44.69 - $49.69/hr

Contract Job Overview: Pay Range: $44.69hr - $49.69hr Requirement/Must Have: * Bachelor s degree ... Strong understanding of GxP and Good Manufacturing Practices (GMP), regulatory requirements, and ...

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Contract Gmp Manufacturing information

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 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 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.

Manufacturing Associate - PIC Suite Operations (7:00 PM - 7:00 AM)

Codis

Seymour, IN • On-site

$20 - $28/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

At Codis (formerly Particle Dynamics), we help transform scientific innovation into real-world health solutions.
As a next-generation global Contract Development & Manufacturing Organization (CDMO), Codis specializes in complex pharmaceutical, nutraceutical, and consumer health manufacturing. With advanced technologies, world-class cGMP operations, and one of the largest commercial spray drying capabilities globally, Codis partners with leading brands to bring high-quality products from development to market safely, efficiently, and reliably.
We are currently seeking a motivated and dependable Production Associate to join our PIC (Polysaccharide Iron Complex) Manufacturing Suite on a permanent rotating 12-hour night shift schedule.
Shift Schedule
This position follows a rotating 2-week pattern:
Week 1
  • Tuesday, Wednesday, Saturday, Sunday
  • 7:00 PM - 7:00 AM
  • 40 regular hours + 8 overtime hours

Week 2
  • Monday, Thursday, Friday
  • 7:00 PM - 7:00 AM
  • 36 regular hours

This rotating schedule repeats continuously.
Pay rate will be based upon experience. Pay range is typically between $20 - $28 hourly.
Position Summary
The Production Associate is responsible for operating and supporting manufacturing processes within the PIC Suite while ensuring compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and safety standards.
This role is hands-on and highly process-driven, involving everything from material weighing and processing to in-process testing, documentation, equipment operation, cleaning, and final product inspection. The ideal candidate is detail-oriented, dependable, safety-conscious, and comfortable working in a fast-paced pharmaceutical manufacturing environment.
Inside the PIC suite, precision matters. Every batch, every reading, every documented step becomes part of a much larger chain that helps deliver quality products customers and patients can rely on.
Essential Duties & Responsibilities
  • Operate manufacturing processes and equipment within the PIC Suite
  • Perform all aspects of manufacturing operations, including:
    • Material weighing
    • Processing
    • In-process testing
    • Final product inspection
    • Packaging
  • Perform additional manufacturing functions such as blending, sifting, milling, and material handling
  • Complete and maintain accurate batch records and manufacturing documentation in accordance with SOPs and cGMP requirements
  • Review batch records and GMP documentation for completeness and accuracy
  • Learn, operate, troubleshoot, and train on PIC Suite unit operations and computer-controlled systems
  • Maintain production equipment and manufacturing areas in a clean and orderly condition
  • Follow all safety procedures, GMP requirements, and company policies
  • Assist with cleaning and sanitation activities within the suite
  • Support other manufacturing areas as needed, including Packaging, Material Handling, and Spray Dryer operations
  • Assist fellow operators and departments upon completion of assigned tasks
  • Participate in continuous improvement and team-oriented manufacturing activities

Qualifications
Education & Experience
  • High school diploma or GED required
  • Previous manufacturing, pharmaceutical, nutraceutical, food production, or industrial experience preferred
  • Experience working in regulated environments is a plus

Knowledge, Skills & Abilities
  • Strong verbal and written communication skills
  • Basic math and reading comprehension skills
  • High level of attention to detail and accuracy
  • Strong organizational and documentation skills
  • Ability to work independently and within a team environment
  • Ability to effectively communicate with coworkers, supervisors, and Quality personnel
  • Ability to learn and operate industrial and manufacturing equipment
  • Forklift and pallet jack experience preferred
  • Commitment to safety, quality, and company values

Physical Requirements
  • Ability to lift 1-50 pounds frequently and repetitively
  • Frequent bending, twisting, squatting, reaching, and repetitive hand movements
  • Ability to stand and walk for extended periods
  • Ability to work in wet conditions during cleaning operations
  • Ability to repeatedly ascend and descend stairs in warm and humid manufacturing environments
  • Ability to independently operate within the PIC Suite environment

Work Environment
  • cGMP-regulated pharmaceutical manufacturing facility
  • Fast-paced, team-oriented production environment
  • Exposure to industrial manufacturing equipment and controlled processing environments
  • Requires strict adherence to documentation, quality, and safety procedures

Why You'll Love Working Here
  • Health, dental, vision, and life insurance effective the 1st of the month following hire
  • 401(k) with immediate vesting
    • 100% match on the first 3%
    • 50% match on the next 2%
  • Paid time off available upon hire (prorated):
    • 80 hours vacation
    • 56 hours sick time
  • 10 paid holidays annually effective upon hire
  • Stable and growing manufacturing environment
  • Opportunities for advancement and cross-training
  • Collaborative culture focused on quality, innovation, and continuous improvement

Codis is proud to be an Equal Opportunity Employer.

Apply