Top 11 Quality control manager Jobs in Portage, In

Manager, Quality Operations
Aquestive Therapeutics Inc. —Portage, IN
- Background check
- Microsoft Excel
- Computer literacy
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Quality Control Manager
Nippon Paint Automotive Americas, Inc. —Lansing, IL
- $89,985.14 - $149,403.00 a year
- Supervising experience
- Bachelor's degree
- Team management
- Paid holidays
- Health insurance
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3d
Quality Manager
Clayco —Hobart, IN
- Full-time
- Construction site
- 5 years
- Residential
- Paid holidays
- Disability insurance
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Civil Construction Quality Control Manager
Central Southern Construction —Chesterton, IN
- Full-time
- Management
- Construction site
- Pass drug screening
- Fuel card
- Paid holidays
Quick Apply
Manager Project Quality
Zachry Group —Kingsbury, IN
- Full-time
- Microsoft Excel
- Management
- Construction site
Quality Manager
Dakkota Integrated Systems —Chicago, IL
- $119,112 - $135,000 a year
- Bilingual
- 7 years
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
Construction Quality Manager
The Walsh Group —La Porte, IN
- Full-time
- Construction site
- Bachelor's degree
- Team management
Land Quality Manager
City Of Gary —Gary, IN
- $45,000 - $48,500 a year
- Full-time
- Management
- Mid-level
- 3 years
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quality control manager jobs near portage, in

Manager, Quality Operations

Aquestive Therapeutics Inc.
Portage, IN

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Job Details

Qualifications

Computer operation
Project management experience in manufacturing
Manufacturing facility experience
Pharmaceutical company experience
Productivity software
Pharmaceutical manufacturing facility experience

Full Job Description

Job Summary:

Responsible for leading day-to-day quality oversight of manufacturing and operational activities to ensure compliance with cGMP, regulatory requirements, and company quality systems. Drives execution, inspection readiness, and continuous improvement across quality operations.

This position will be expected to work in a highly collaborative, cross functional team environment, and provide expert knowledge to risk identification/mitigation, strategy and execution.

Responsibilities:

Daily GMP Oversight (Shop Floor + Operations), providing real-time QA oversight of manufacturing and packaging activities of a multi-site, multi-shift operation.
Manage the product quality release program, ensuring on-time results and adherence to internal procedures.
Provide quality risk assessment and decision support real-time, including containment correction measures.
Review and release of batch records.
Author, review and/or approve quality documentation related to manufacturing.
Ensure adherence to SOPs, batch records, and GMP requirements
Lead and/or oversee deviations, OOS, complaints, and investigations, ensuring robust root cause analysis and effective CAPAs.
Manage Quality Operations personnel, setting priorities, staffing plans and shift coverage.
Manage incoming materials quality review/approval to ensure materials are appropriately received, assessed, and released for use in accordance with applicable procedures.
Coach team on GMP decision-making, risk-based quality judgement and investigator rigor.
Monitor and report key quality metrics, including right first time.
Identify trends and drive process improvements and simplification.
Ensure continuous state of audit readiness, supporting health authority inspections and internal audits.
Act as a primary QA partner to Manufacturing, Quality Control and Supply Chain and Quality Systems.

Qualifications:

Education: Bachelor’s degree (Science, Engineering, or related)
Experience: ~7–10 years in GMP pharmaceutical manufacturing QA/QC
Leadership: Prior people management or strong informal leadership
Expertise:
- cGMP regulations (FDA / EU)
- Quality systems (CAPA, deviations, change control)
- Manufacturing and/or QC operations

Excellent computer skills required (e.g., Microsoft Word, Excel, Access, PowerPoint, Visio).
Strong project management skills, strong organizational skills to maintain a high level of productivity, innovation, and priority-setting to complete assignments on time and on budget.
Strong business acumen surrounding pharmaceutical manufacturing.
Some travel required.

The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.

As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place.

Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

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quality control manager jobs in portage, in

Manager, Quality Operations

Quality Control Manager

Quality Manager

Civil Construction Quality Control Manager

Manager Project Quality

Quality Manager

Construction Quality Manager

Land Quality Manager

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