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63 Power Design Quality Control Supervisor Jobs Hiring Near You

Cambrex

Quality Control Supervisor

Charles City, IA · On-site

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 ...

Dixon

Quality Control Supervisor

Chestertown, MD

$65K - $90K/yr

Quality Control Supervisor Location: This role is based out of two Chestertown, MD locations, with ... Facilitate regular cross-departmental meetings, bridging gaps between design intent and ...

Ruhrpumpen, Inc.

Quality Control Supervisor

Tulsa, OK · On-site

QUALITY CONTROL SUPERVISOR Key Responsibilities Leadership & Team Management * Supervise, lead, schedule, and train quality control inspectors. * Mentor and coach QC staff on inspection methods ...

Boise Cascade

Quality Control Supervisor

Chester, SC

$80K - $95K/hr

The Quality Control Supervisor is responsible for the quality of the product manufactured on his or her assigned shift. This person is also responsible for developing and implementing testing ...

PBV

QC Supervisor

Garner, NC · On-site

Pepsi Bottling Ventures is seeking a QC Supervisor to join our team! Who We Are We are jointly owned by Suntory and PepsiCo. Suntory is a family-owned business founded in Japan more than 125 years ...

MOBIS

Quality Control Supervisor

GA · On-site

Summary The QC Supervisor is responsible for planning and directing activities concerned with the development, application, and maintenance of quality standards for processes, materials, and products.

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Power Design Jobs Information

What makes Power Design an attractive place to work?

Power Design is a reputable company in the industry, known for its commitment to delivering innovative and efficient power solutions. The company's workplace is characterized by a collaborative environment that fosters creativity, open communication, and a culture of continuous learning, with opportunities for professional growth and development. Joining Power Design offers the chance to contribute to the development of cutting-edge technologies and be part of a dynamic team that values innovation, teamwork, and employee growth.
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Infographic showing various Quality Control Supervisor job openings at Power Design in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Quality Control Supervisor

Cambrex

Charles City, IA • On-site

Full-time

Medical, Life, Retirement

Posted 29 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

Workplace

Get the full story on Breakroom

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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

Social media

Twitter

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