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Q Pharma Jobs (NOW HIRING)

Techtrueup

C&Q Engineer

New Albany, OH

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Commissioning & Qualification (C&Q) Engineer Location: Ohio Duration: 6 months Shift: 1st shift (7 ...

Techtrueup

C&Q Engineer

New Albany, OH · On-site

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Commissioning & Qualification (C&Q) Engineer Location: Ohio Duration: 6 months Shift: 1st shift (7 ...

Techtrueup

C&Q Engineer

New Albany, OH · On-site

... including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food ... Commissioning & Qualification (C&Q) Engineer Location: Ohio Duration: 6 months Shift: 1st shift (7 ...

PharmEng Technology Americas

PR · On-site

URS, C&Q Plan, risk assessments), authoring protocols, execution of commissioning and qualification ... It releases groups from paper and is presently being used by 12 of the world's top 20 pharma ...

Mirus Consulting Group

Project Manager

Manati, PR · On-site

Project Management experience in regulated industries (Pharma, Biotech, Life Sciences) * Proven experience managing facility modifications or capital projects * Working knowledge of C&Q processes

Mirus Consulting Group

MES Project Manager

Manati, PR · On-site

$83K - $98K/yr

Project Management experience, preferably in Pharma or Life Sciences * Proven experience with MES implementations, preferably Syncade * Strong understanding of system validation and C&Q * Experience ...

Mirus Consulting Group

MES Project Manager

Manati, PR · On-site

$83K - $98K/yr

Project Management experience, preferably in Pharma or Life Sciences * Proven experience with MES implementations, preferably Syncade * Strong understanding of system validation and C&Q * Experience ...

Mirus Consulting Group

Project Manager

Manati, PR · On-site

Project Management experience in regulated industries (Pharma, Biotech, Life Sciences) * Proven experience managing facility modifications or capital projects * Working knowledge of C&Q processes

PharmEng Technology Americas

PR · On-site

C & Q PharmEng Technology has been providing quality services to leading manufacturers of health ... It releases groups from paper and is presently being used by 12 of the world's top 20 pharma ...

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How much do q pharma jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for q pharma in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.48 and $63.70 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Q Pharma position, and why are they important?

To thrive in a Q Pharma role, candidates typically need a background in pharmaceutical sciences, quality assurance, or regulatory affairs, often supported by a relevant degree. Familiarity with industry-standard tools and systems such as GMP (Good Manufacturing Practices), LIMS (Laboratory Information Management Systems), and FDA or EMA regulatory standards is crucial. Strong attention to detail, analytical thinking, and excellent communication skills help professionals excel in this position. These competencies ensure pharmaceutical products meet strict quality standards and regulatory compliance, safeguarding consumer safety and organizational reputation.

What is a Q Pharma job?

A Q Pharma job typically refers to a position within the pharmaceutical industry that focuses on quality assurance, quality control, or regulatory compliance. Professionals in these roles ensure that pharmaceutical products meet industry standards, regulatory requirements, and safety guidelines. Responsibilities may include reviewing manufacturing processes, conducting audits, and maintaining documentation to comply with FDA and other regulatory bodies. These jobs are critical for maintaining product integrity and patient safety in the pharmaceutical sector.

What are the main responsibilities of someone working in a Q Pharma position?

In a Q Pharma role, your core responsibilities typically include monitoring product quality throughout the manufacturing process, conducting inspections and audits, maintaining meticulous documentation, and ensuring compliance with regulatory guidelines. You might also be involved in investigating quality issues, developing process improvements, and coordinating with production, R&D, and regulatory teams. The position often requires balancing multiple projects while supporting both routine operations and new product introductions. Success relies on close collaboration with cross-functional departments to ensure quality standards are consistently maintained.

More about Q Pharma jobs
What job categories do people searching Q Pharma jobs look for? The top searched job categories for Q Pharma jobs are:
Q Pharma jobs near you
Infographic showing various Q Pharma job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 96% Full Time, 1% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $113,000 per year, or $54.3 per hour.

C&Q Engineer

Techtrueup

New Albany, OH

Contractor

Posted 14 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.

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