Top 9117 Associate Manager Packaging Jobs

Associate Manager/Manager, Quality Assurance
Granules Pharmaceuticals —Chantilly, VA
- $115,000 a year
- Full-time
- Computer literacy
- Mid-level
- Master's degree
Quick Apply
Packaging Associate
Hendler Family Brewing Co. —Framingham, MA
- $20 - $22 an hour
- Full-time
- Forklift
- High school diploma or GED
- 21 years or older
- Health insurance
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Manufacturing Associate
Web Industries Inc —Suwanee, GA
- Full-time
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- Basic math
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Repack Associate - Produce
Sanwa Food Group —Tampa, FL
- Ability to lift 50 pounds
- Quality control
- Warehouse experience
- Paid holidays
- Dental insurance
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Shipping (1st Shift | 2nd Shift)
Exential —Colchester, VT
- $21.63 - $24.51 an hour
- Full-time
- Microsoft Outlook
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Operations Admin/ WHS Specialist
Quality Packaging —Oxnard, CA
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National Raisin Company —Fowler, CA
- $90,000 - $120,000 a year
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- Management
- Health savings account
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PRESS OPERATOR
ABX Innovative Packaging Solutions, LLC —Macedon, NY
- $19.00 - $21.50 an hour
- 12 hour shift
- Basic math
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Warehouse Worker / Backup Delivery Driver - Building Materials
Hardwoods Specialty Products —San Luis Obispo, CA
- $18 - $22 an hour
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Customer Account Specialist
Magris Talc —Three Forks, MT
- $47,137 - $58,921 a year
- Full-time
- 5 years
- Mid-level
- Associate's degree
Packaging Warehouse Supervisor
Western Sugar Cooperative —Scottsbluff, NE
- $80,000 - $90,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Relocation assistance
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Manufacturing Associate OT Franklin
First Call Temporary Services —Franklin, IN
- Weekends as needed
- 18 years or older
- No experience needed
- Assembly
- 401(k) matching
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SUPPLY CHAIN / PRODUCTION PLANNING MANAGER
Buddeez, Inc. —Union, MO
- $65,000 - $80,000 a year
- Overtime
- Inventory management
- Mid-level
- 3 years
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8d
Manager, Drug Enforcement Administration
Catalent —Kansas City, MO
- Email
- Management
- 5 years
- Bachelor's degree
- Paid holidays
- Relocation assistance
Open Box Assurance (OBA) Supervisor
Quanta Manufacturing Fremont —Fremont, CA
- $72,000 - $90,000 a year
- Full-time
- Spanish
- 5 years
- English
- Health insurance
- Dental insurance
Quick Apply
14d
Quality Assurance Technician - Food Manufacturing
Carolina Ingredients, LLC —Rock Hill, SC
- $20 - $23 an hour
- Full-time
- Background check
- Writing skills
- Laboratory experience
- Health savings account
- Health insurance
Quick Apply
CDL Class A Yard Driver
Primo Brands —Kingfield, ME
- $28.73 an hour
- Weekends as needed
- Customer service
- English
- CDL A
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14d
Prepress Supervisor
Charter Next Generation —Green Bay, WI
- From $34 an hour
- Full-time
- 7 years
- Microsoft Excel
- Pass drug screening
- Paid holidays
- Health insurance
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Sales Manager
Confidential —Harwich, MA
- $100,000 - $175,000 a year
- Weekends as needed
- Microsoft Outlook
- 5 years
- Merchandising
- Relocation assistance
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International Trade Compliance Manager
Ace Hardware Corporation —Oak Brook, IL
- $137,700 - $175,600 a year
- Full-time
- Spanish
- 7 years
- English
- Paid holidays
- Disability insurance

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Associate Manager/Manager, Quality Assurance

Granules Pharmaceuticals -
Chantilly, VA

Quick Apply

Job Details

Full-time
$115,000 a year

Qualifications

USP standards
Computer operation
Drug regulation
Technical writing experience within manufacturing
Manufacturing facility experience
ICH guidelines
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Compliance documentation
Desktop applications
Productivity software
Cross-functional collaboration
Cross-functional communication
FDA regulations
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.

The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications. This position is responsible for performing documentation for all quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.

Job Duties & Responsibilities

The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements.
Managing all quality operations to include inspection of components, bulk, and final products for the Chantilly, VA, ensuring release lead times are met with timely product disposition.
Ensure that the facility is meeting all training requirements.
Lead the communication of open quality document notification and resolution between all departments regarding Complaints, Investigations, Change Control, CAPA’s (including verification of CAPA’s) and other quality documents as needed.
Manage and maintain audit inspections (Internal and External) for the site.
Responsible for supporting the preparation, review, processing, and approval of various validation documents as application for the Granules, Chantilly, facility.
Provide QA support, review and approval for relevant documents including relevant procedures, batch records, specifications, stability reports, technical reports (i.e., Qualification, Validation, Transportation.), trend reports, Annual Product Quality Reviews and other documents as needed.
Responsible for performance and development of all Quality Assurance staff through mentoring and focusing on personal and professional growth.
Work with Quality leadership team for proactive succession planning and a high-performance culture through people.
Guide and lead by setting realistic personal goals for staff and provide regularly scheduled feedback throughout the year.
Provide the means for incorporating the necessary tools, equipment, and methods into the new and existing processes aimed at continuous improvement.
Implementation Quality management system tools and their compliance.
Development and execution of quality training modules for the organization.
Ensure staff receives appropriate knowledge and skill development and growth opportunities
Work with Regulatory Affairs to supply information needed for FDA filings.
Other duties as assigned by management.

Requirements:

Knowledge & Skills

Expert-level knowledge of the FDA guidance for Industry, Title 21 of the Code of Federal Regulations and Compendia (USP/EP/BP/etc...)
cGMP compliance within the pharmaceutical manufacturing industry.
Writing and maintaining cGMP documentation.
Analyze data/information and resolve complex issues.
Verbal and written communication skills.
Work and communicate with cross-functional teams.
Multiple priorities and re-prioritize tasks.
Strong computer skills and working knowledge of Microsoft Office Suite and Adobe
Demonstrated ability to work on complex assignments in collaboration with various departments.

Experience & Education

Bachelor's degree in the life sciences (or equivalent work experience) minimum of 6+ years in a QA role within the pharmaceutical industry
Master’s degree with 4+ years of pharmaceutical manufacturing experience and at least 3 years of those years in a progressive challenging QA department in the pharmaceutical industry.

Physical Requirements/Working Environment

While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
Specific vision abilities required by this job include close vision requirements due to computer work.
Ability to sit at a computer terminal for an extended period of time.
Light to moderate lifting up to 10-15 lbs is required.
Ability to work in a confined area

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

Quick Apply

Refine Your Search

Associate Manager Packaging jobs

Associate Manager/Manager, Quality Assurance

Packaging Associate

Manufacturing Associate

Repack Associate - Produce

Shipping (1st Shift | 2nd Shift)

Operations Admin/ WHS Specialist

Food Safety and Compliance Manager

PRESS OPERATOR

Warehouse Worker / Backup Delivery Driver - Building Materials

Customer Account Specialist

Packaging Warehouse Supervisor

Manufacturing Associate OT Franklin

SUPPLY CHAIN / PRODUCTION PLANNING MANAGER

Manager, Drug Enforcement Administration

Open Box Assurance (OBA) Supervisor

Quality Assurance Technician - Food Manufacturing

CDL Class A Yard Driver

Prepress Supervisor

Sales Manager

International Trade Compliance Manager

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