Top 7 Quality control manager Jobs in Warrenton, Va

Quality Control Manager
Granules Pharmaceuticals —Chantilly, VA
- $100,000 - $120,000 a year
- Bachelor of Science
- Bachelor's degree
- Team management
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Quality Manager
Sciolex Corporation —Chantilly, VA
- Full-time
- 5 years
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Data Center Construction Quality Assurance Manager
Worldwide Mission Critical LLC —Chantilly, VA
- CPR Certification
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RWD Consulting, LLC —Falls Church, VA
Bachelor’s degree in a related field. In this pivotal role, you will oversee the implementation and maintenance of quality systems, ensuring compliance with…
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Quality Assurance (QA) Lead
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Bachelor’s degree in Engineering, Computer Science, or related technical field and 8–12 years of relevant experience, or Master’s degree with 6–10 years of…
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QC Supervisor
WESTERMAN INC —Hebron, OH
Assists teams (including maintenance and engineering) with continuous improvement initiatives (driving safety, quality and process efficiencies).
$85,000 - $95,000 a year
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14d
QC Supervisor
WESTERMAN INC —Bremen, OH
Assists teams (including maintenance and engineering) with continuous improvement initiatives (driving safety, quality and process efficiencies).
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quality control manager jobs near warrenton, va

Quality Control Manager

Granules Pharmaceuticals -
Chantilly, VA

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Job Details

$100,000 - $120,000 a year

Qualifications

Biotechnology
Performance management
Managing laboratory teams
Bachelor's degree
Team management
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
General management
Pharmaceutical manufacturing facility experience

Full Job Description

Description:

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary

Supervise the work of laboratory personnel engaged in performing routine finished product testing & stability testing, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems. Execute according to high standards of quality at the lab through managing and continuously improving the effectiveness of laboratory quality processes and systems

Job Duties & Responsibilities

Supervise the testing of bulk release, finished product and stability testing
Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure assigned tasks are performed.
Review of test results for accuracy and proper documentation.
Review of specifications and STMs for in process and finished products.
Write OOS investigations, including finding root cause and corrective/preventive actions.
Supervise lab processes, including timely management of investigations, CAPA implementation to ensure sustainable compliance
Review of SOPs, lab related investigations, stability failure notifications, COAs, and compilation of stability related data. Responsible for timely release of in-process, finished product release COA’s
Monitor and report the trends in bulk, finished products, and stability samples to QC/QA Management
Review of IQ, OQ, and PQ for new instruments, protocols/reports
Responsible for coordinating with other departments like warehouse, QA, Maintenance, purchase department, R&D in day to day activity for better operational requirements and to follow the cGMP requirements.
Responsible for the coordination of sample management, not limited to in-process, finished product and stability samples.
Monitor Quality Control, Safety and cGMP practices to assure compliance with internal and external regulations.
Perform other related duties as assigned to meet departmental and Company objectives.

Management Responsibility

Manage group of scientists.

Reports to

Associate Director / Director

Requirements:

Knowledge & Skills

Ability to maintain integrity and honesty at all times
Ability to communicate and lead with transparency
Accountable for performance and results of department
Ability to assume additional responsibilities on own initiative.

Experience & Education

Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years’ experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.

Physical Requirements/Working Environment

Regular Laboratory environment with lab coats, safety glasses, 4-6hrs/day of standing while performing chemical test and able to stand for 4-6hrs/day.

Travel

No Travel requirement.

Disclaimer

The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.

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