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30 Techtrueup Product Manufacturing Jobs Hiring Near You

... product. This is not a validation role--we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a ...

... product. This is not a validation role-we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a ...

... product. This is not a validation role-we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a ...

Machine Operator (GMP)- 2nd shift

Clinton, PA · On-site

$16.75 - $20/hr

The GMP Associate I supports the manufacturing of high-quality medical devices by operating equipment, packing finished products, loading automatic hoppers, and resolving basic equipment faults ...

The GMP Associate I supports the manufacturing of high-quality medical devices by operating equipment, packing finished products, loading automatic hoppers, and resolving basic equipment faults ...

... Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software ... Review risk documentation and product labeling based on clinical data. * Manage clinical ...

... Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software ... Review risk documentation and product labeling based on clinical data. * Manage clinical ...

Facilities Assistant

Clinton, PA · On-site

$37.10K - $46.10K/yr

... Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software ... This could include working with Production and maintenance staff. • Verifies effectiveness of ...

... Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software ... Review risk documentation and product labeling based on clinical data. * Manage clinical ...

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TechTrueUp Jobs Information

What are the key skills and qualifications needed to thrive in Product Manufacturing, and why are they important?

To thrive in Product Manufacturing, a solid understanding of production processes, quality control, and safety protocols is essential, often supported by a relevant technical degree or vocational training. Familiarity with manufacturing equipment, ERP systems, and industry certifications like Six Sigma or Lean Manufacturing are highly valued. Strong attention to detail, teamwork, and effective problem-solving skills help individuals excel in this environment. These competencies ensure efficient production, high-quality output, and the ability to adapt to process improvements and challenges.

What are some common challenges faced in a Product Manufacturing role and how can they be managed?

Product Manufacturing professionals often encounter challenges such as maintaining quality standards while meeting tight production deadlines, adapting to changes in demand, and troubleshooting equipment issues. Effective communication with team members and other departments, such as engineering and quality assurance, is key to quickly resolving issues and keeping production on track. Utilizing lean manufacturing principles and continuous improvement strategies can help teams address inefficiencies and reduce waste, contributing to a smoother workflow and better product outcomes.

What is product manufacturing?

Product manufacturing is the process of producing goods on a large scale using labor, machinery, tools, and chemical or biological processing. It involves transforming raw materials into finished products that are ready for sale or distribution. This process can include designing, engineering, assembling, and quality testing to ensure products meet required standards. Product manufacturing is a critical part of many industries, including electronics, automotive, food, and textiles.

What is the difference between Product Manufacturing vs Product Assembly?

AspectProduct ManufacturingProduct Assembly
CredentialsTechnical certifications, manufacturing trainingBasic technical skills, assembly training
Work EnvironmentFactories, production linesWorkstations, assembly lines
Industry UsageMass production, large-scale factoriesFinal product setup, component fitting

Product manufacturing involves the entire process of creating products from raw materials, including designing, fabricating, and testing. Product assembly focuses on putting together components to complete the final product. While manufacturing covers the broader process, assembly is a key step within it, often requiring less specialized credentials but essential for completing the product.

Infographic showing various Product Manufacturing job openings at Techtrueup in the United States as of May 2026, with employment types broken down into 100% Contract. Highlights an 84% Physical, 8% Hybrid, and 8% Remote job distribution.

C&Q Engineer

Techtrueup

New Albany, OH

Contractor, Other

Posted 3 days ago


Job description

Company Description

Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition.

Job Description

Title: Commissioning & Qualification (C&Q) Engineer
Location: Ohio
Duration: 6 months
Shift: 1st shift (7:00am – 4:00pm)  | 2nd shift (3:00pm – 11:00pm)
Job Description :

We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to join our team in support of a major capital expansion project involving the installation of four new packaging lines. This is a hands-on C&Q role embedded within a pharmaceutical secondary and tertiary packaging operation for final drug product. This is not a validation role—we are looking for a true C&Q professional with deep expertise in equipment commissioning, system turnover, and manufacturing process knowledge within a regulated pharmaceutical environment.
You will be responsible for leading and executing commissioning and qualification activities across new packaging equipment installations, ensuring all systems are built, installed, and functionally verified to specification and ready for handover to GMP manufacturing operations.
Key Responsibilities

  • Lead and execute commissioning and qualification activities for new secondary and tertiary packaging equipment installations across four new packaging lines in Building 2
  • Develop, author, review, and execute C&Q documentation including commissioning plans, commissioning protocols, test scripts, punch lists, and turnover packages
  • Perform hands-on equipment walkdowns, system verifications, and commissioning checks directly on the manufacturing floor
  • Manage punch list identification, tracking, and resolution through to system acceptance and turnover
  • Collaborate with equipment vendors, engineering, construction, and operations teams to ensure systems are installed, functional, and commissioned to design specification
  • Support and execute SAT (Site Acceptance Testing) activities for incoming packaging equipment
  • Ensure all C&Q activities are performed in compliance with FDA, GMP, and applicable site and regulatory standards
  • Apply manufacturing process knowledge to ensure commissioning scope and acceptance criteria reflect real-world operational requirements
  • Partner with Quality, Manufacturing, and Engineering to support a clean, compliant turnover of commissioned systems into GMP operations
  • Maintain accurate and complete C&Q records in compliance with site documentation standards and data integrity requirements.
Additional Information

All your information will be kept confidential according to EEO guidelines.