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Quality Control Program Manager Jobs in Iowa (NOW HIRING)

Reporting to the Manager, QC, the QC Supervisor will provide supervisory oversight, laboratory ... programs. May need to assist with troubleshooting and minor repairs. * Support training and ...

Job Overview Reporting to the Manager, QC, the QC Supervisor will provide supervisory oversight ... programs. May need to assist with troubleshooting and minor repairs. * Support training and ...

Job Overview Reporting to the Manager, QC, the QC Supervisor will provide supervisory oversight ... programs. May need to assist with troubleshooting and minor repairs. * Support training and ...

Quality Control Technician

Carlisle, IA · On-site

$18.25 - $23.25/hr

... management to ensure that all Quality Control duties are performed. * Work closely with production personnel on meeting and exceeding product quality. * Support safety and production programs.

QC Technician

Cedar Rapids, IA · On-site

$18.50 - $23.50/hr

The electrical QC Technician will ensure that the materials and work meet the quality standards ... Employee Discount Program through PerkSpot * Tax Savings Accounts - FSA, HSA, DCFSA and CSA

Quality Control Technician

Carlisle, IA · On-site

$18.25 - $23.25/hr

... management to ensure that all Quality Control duties are performed. * Work closely with production personnel on meeting and exceeding product quality. * Support safety and production programs.

QC Technician

Cedar Rapids, IA

$18.50 - $23.50/hr

The electrical QC Technician will ensure that the materials and work meet the quality standards ... Employee Discount Program through PerkSpot * Tax Savings Accounts - FSA, HSA, DCFSA and CSA

QC Technician

Cedar Rapids, IA

$18.50 - $23.50/hr

The electrical QC Technician will ensure that the materials and work meet the quality standards ... Employee Discount Program through PerkSpot * Tax Savings Accounts - FSA, HSA, DCFSA and CSA

Quality Control Technician

Tipton, IA

$16.50 - $21.25/hr

Position Summary Reporting to the Plant Manager, the Quality Control Technician plays a critical ... Actively support workplace safety programs, hazard assessments, and standard operating procedures ...

Showing results 21-40

Quality Control Program Manager information

What is a quality control program manager?

Quality Control Program Managers are professionals who oversee and coordinate quality assurance activities within an organization. They develop, implement, and maintain quality control systems to ensure that products or services meet established standards and regulatory requirements. These managers lead teams, conduct audits and inspections, analyze quality data, and collaborate with other departments to resolve quality issues. Their role is critical in minimizing defects, improving processes, and ensuring customer satisfaction.

How does a quality control program manager typically collaborate with cross-functional teams to ensure product standards are met?

A Quality Control Program Manager regularly works alongside teams such as manufacturing, engineering, regulatory affairs, and supply chain to align quality standards across all stages of production. This collaboration often involves participating in cross-functional meetings, reviewing process documentation, and leading corrective action initiatives when deviations occur. By fostering open communication and implementing feedback loops, the manager ensures that quality objectives are understood and met company-wide, minimizing errors and supporting continuous improvement.

What are the key skills and qualifications needed to thrive as a quality control program manager, and why are they important?

To thrive as a Quality Control Program Manager, you need expertise in quality assurance methodologies, data analysis, and process improvement, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), Six Sigma certification, and proficiency in statistical software are typically required. Strong leadership, problem-solving abilities, and effective communication skills help you lead teams and drive compliance. These competencies are crucial to ensure product quality, regulatory adherence, and continuous organizational improvement.

What is the difference between Quality Control Program Manager vs Quality Assurance Specialist?

AspectQuality Control Program ManagerQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, Six SigmaISO 9001 Internal Auditor, Six Sigma Green Belt
Work EnvironmentOversees quality control processes across projects, often in manufacturing or production settingsFocuses on developing and implementing quality assurance procedures, typically in labs or office settings
Employer & Industry UsageManufacturing, aerospace, automotive, constructionPharmaceuticals, software, manufacturing, healthcare

The Quality Control Program Manager primarily manages and oversees quality control processes to ensure products meet standards, while the Quality Assurance Specialist develops and maintains quality assurance systems to prevent defects. Both roles require similar certifications and work in related environments, but their focus differs: control vs. assurance.

What are popular job titles related to Quality Control Program Manager jobs in Iowa?

For Quality Control Program Manager jobs in Iowa, the most frequently searched job titles are:

Quality Control Supervisor

Cambrex

Charles City, IA • On-site

Full-time

Medical, Life, Retirement

Re-posted 5 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

Reporting to the Manager, QC, the QC Supervisor will provide supervisory oversight, laboratory testing support, and technical leadership for laboratory staff. The QC Supervisor will be responsible for directing the laboratory workflow for daily testing of isolated intermediates, finished goods, and stability and providing on-going support for these activities.

Responsibilities:
  • Coordinate daily prioritization of QC testing, including staff and equipment utilization. 
  • Maintain laboratory instrumentation, including equipment qualification, and preventative maintenance programs. May need to assist with troubleshooting and minor repairs. 
  • Support training and troubleshooting efforts for staff. 
  • As necessary, review completed laboratory testing to support the timely release of data, reports, and material. 
  • Coordinate and oversee the status of offsite sample testing.  
  • Maintain and manage cGMP and general lab systems at defined levels of compliance. 
  • Draft and review various documents in support of laboratory efforts and production campaigns. 
  • Maintain laboratory systems and documentation. 
  • On a rotating coverage, provide laboratory on-call support coverage for all aspects of laboratory operation, including environmental testing, raw material testing, in-process testing, isolated intermediate testing, and finished good product release. 
  • Work cross-functionally with other departments (such as Operations/Production) to ensure deliverables are met according to projected timelines.  
  • Verify timecards and SAP billing is completed accurately and on time as per the site-specific timelines. 
  • Perform the QC release for raw materials, isolated intermediates, and finished goods. 
  • Identify discrepancies, author out of specification and deviation investigations within TrackWise, and implement associated CAPAs.  
Qualifications / Skills:
  • Familiarity with compliance requirements within cGMP, safety and regulatory environments 
  • Operational knowledge of analytical instrumentation like HPLC/UPLC, GC, IC. ICP, FTIR, UV-VIS equipment, and data stations required 
  • Demonstrated computer literacy, including word processing, spreadsheets, structural drawings, and databases preferably in a Windows environment  
  • Strong chemistry knowledge 
Education, Experience, and Licensing Requirements: (Text Only)  - Bachelor's Degree in Chemistry, Pharmacy or closely related field required. Advanced degree highly beneficial.  - 5 or more years of experience in manufacturing support laboratory in the pharmaceutical industry, preferably API and/or intermediate experience.  - Hands on experience with pharmaceutical laboratory management required. Management of 24/7 lab operation highly beneficialEmployment Type: FULL_TIME

What Cambrex employees say

Pay

Benefits

Hours and flexibility

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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