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Hourly Upstream Manufacturing Associate Jobs in Indiana

This position will be a direct supervisor to a team of manufacturing associates. Production ... Train, coach, mentor and lead plant hourly employees for improved performance. * Encourage and ...

This position will be a direct supervisor to a team of manufacturing associates. Production ... Train, coach, mentor and lead plant hourly employees for improved performance. * Encourage and ...

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Hourly Upstream Manufacturing Associate information

What is the difference between Hourly Upstream Manufacturing Associate vs Upstream Manufacturing Technician?

AspectHourly Upstream Manufacturing AssociateUpstream Manufacturing Technician
CredentialsHigh school diploma or equivalent; GMP training often requiredHigh school diploma; GMP and technical training
Work EnvironmentManufacturing floor, repetitive tasks, team-basedManufacturing floor, technical troubleshooting, equipment operation
Employer & Industry UsageBiotech and pharmaceutical manufacturingBiotech and pharmaceutical manufacturing
Common Search & ComparisonYesYes

The main difference between an Hourly Upstream Manufacturing Associate and an Upstream Manufacturing Technician lies in their roles and responsibilities. Associates typically perform routine manufacturing tasks under supervision, focusing on production line activities. Technicians often have more technical training, handle troubleshooting, and maintain equipment. Both roles are essential in biotech manufacturing, with similar credentials and work environments, but technicians usually require additional technical skills.

What are popular job titles related to Hourly Upstream Manufacturing Associate jobs in Indiana? For Hourly Upstream Manufacturing Associate jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Hourly Upstream Manufacturing Associate jobs in Indiana look for? The top searched job categories for Hourly Upstream Manufacturing Associate jobs in Indiana are:
What cities in Indiana are hiring for Hourly Upstream Manufacturing Associate jobs? Cities in Indiana with the most Hourly Upstream Manufacturing Associate job openings:
Inspection Associate, 2nd shift

Full-time, Other

Re-posted 21 days ago


Job description

Inspection Associate Summary

INCOG BioPharma Services is seeking a subject matter expert (SME) with capabilities in the inspection and of sterile drug products. The Inspection Associate is a key role within the organization. The ideal candidate must have experience in the inspection of pharmaceutical drug products.

The primary responsibility of the Inspection Associate is to perform continuous inspection to identify and remove critical, major, and minor defects from finished product according to standard procedures. They will be responsible for meeting/exceeding production standards, maintaining product quality, and minimizing/preventing equipment downtime. The ideal candidate will ensure compliance with quality systems, policies, procedures, and cGMP practices and collaborate effectively with internal partners, clients, and vendors.

The hours for the Inspection Associate, 2nd Shift are 2:00pm - 10:30pm.

Essential Job Functions:

  • Follow production and manufacturing procedures.
  • Inspect filled product container for cosmetic, particle and integrity defects.
  • Assist in writing and implementing area’s process documents.
  • Operate equipment in compliance with SOPs.
  • Assure compliance with cGMP requirements (current good manufacturing practices).
  • Perform label and packaging activities for finished product.
  • Complete and review associated production records.
  • Train new inspectors in accordance with inspector certification procedures.
  • Assist other manufacturing functions (Formulation, Fill, Materials) as required.
  • Perform duties gowned in Grade C, D, and controlled non-classified cleanrooms.
  • Perform cleaning and sanitization activities as needed.
  • Collaborate and communicate with cross functional teams.
  • Work flexible hours to ensure production facility coverage.


Special Job Requirements:

  • High School diploma required, minimum 1 year of GMP pharmaceutical experience in drug product inspection and/or packaging.
  • Must pass health and visual check and eye inspections annually for visual acuity and color blindness. Failure in vision test or annual recertification could result in termination.

Additional Preferences:

  • Good math and documentation skills.
  • Ability to perform repetitive tasks.
  • Ability to learn and adapt to innovative ideas.
  • Good observation skills.
  • Initiative-taking and Collaborative.
  • Effective organization skills and diligent.
  • Ability to work with minimal supervision.

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.

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.

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