Top 19 Control supervisor Jobs in Charles City, Ia

Quality Control Supervisor
Cambrex Corp. —Charles City, IA
- On call
- 5 years
- Word processing
- Computer literacy
- Health insurance
- Life insurance
Quality Control Supervisor
Cambrex —Charles City, IA
- Full-time
- 5 years
- Word processing
- Computer literacy
Service Supervisor - Des Moines, IA (Student Living) R0197958 Remote Iowa Full time
Greystar —Iowa
- $26 - $28 an hour
- Email
- Mid-level
- Team management
- Apartments
- Paid parental leave
- Paid holidays
4d
Quality Control Manager
Zoetis —Charles City, IA
- Overtime
- Microsoft Word
- 7 years
- Microsoft Excel
Lube Center Manager
Express Care —Charles City, IA
- Full-time
- Mid-level
- Ability to climb stairs
- High school diploma or GED
- Flexible schedule
Quick Apply
10d
Construction Quality Control Manager- USACE
Thalle Construction Company —United States
- Full-time
- Construction site
- Senior level
- Leadership
- Paid holidays
- Disability insurance
Quick Apply
13d
Project Manager - Air Quality
SWCA Environmental Consultants —United States
- $102,047.40 - $134,152.20 a year
- Online Application
- Remote
- 7 years
- Bachelor of Science
- Engineering
- Profit sharing
- Health insurance
Sr. Engineering Manager, Film
Novolex —United States
- $155,000 - $170,000 a year
- Full-time
- Engineering
- Travel
- Senior level
- Wellness program
- Paid parental leave
Project Manager/Engineer - Water Treatment
ENTACT —United States
- Online Application
- Microsoft Excel
- Microsoft Outlook
- Construction site
- Health insurance
- Dental insurance
Quick Apply
Construction SCADA Controls Manager I and II- Solar
M. A. Mortenson Company —United States
- $125,600 - $216,500 a year
- Up to 50% travel
- Construction site
- Customer service
- AD&D insurance
- Paid holidays

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Quality Control Supervisor

Cambrex Corp. -
Charles City, IA

Apply Now

Job Details

Benefits

Health insurance
Life insurance

Qualifications

Manufacturing facility experience
Managing laboratory teams
Supervising experience
Bachelor's degree
Pharmaceutical company experience
Gas chromatographs
Fourier-transform infrared (FTIR) spectroscopy
Ultraviolet-visible spectrometers
Pharmaceutical manufacturing facility experience

Full 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!

Job 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 & Licensing Requirements

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 beneficial

Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration.

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.

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control supervisor jobs in charles city, ia

Quality Control Supervisor

Quality Control Supervisor

Service Supervisor - Des Moines, IA (Student Living) R0197958 Remote Iowa Full time

Quality Control Manager

Lube Center Manager

Construction Quality Control Manager- USACE

Project Manager - Air Quality

Sr. Engineering Manager, Film

Project Manager/Engineer - Water Treatment

Construction SCADA Controls Manager I and II- Solar

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