ZipRecruiter

Log In

1

Associate Director Gmp Quality Systems Jobs (NOW HIRING)

Viking Therapeutics

Director, Quality Systems

San Diego, CA · On-site

$170K - $210K/yr

The Director Quality Systems will lead and support quality assurance and quality systems activities ... The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and ...

MSD

Associate Director Quality

West Point, PA

Has a deep understanding of GMP and EHS compliance and compliance risk. * Working Across Boundaries ... Production System experience. * LSS Green Belt certification or equivalent experience.

New

Lupin Somerset

NY · On-site

Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... Quality Systems. * Issuance of GMP documents i.e. logbooks, notebooks, batch records, etc.

Wave Life Sciences

Director, Quality Systems

Boston, MA · On-site

$193K - $261K/yr

Description The Director, Quality Systems (QS) leads the internal team at Wave responsible for ... This role is primarily focused on supporting GMP areas with some support of GXP. This is an onsite ...

New

previous page

Showing results 41-60

All JobsTechnology JobsSoftware JobsDirector Of Software Development JobsAssociate Director Gmp Quality Systems Jobs

Associate Director Gmp Quality Systems information

See salary details

$31K

$125.6K

$213.5K

How much do associate director gmp quality systems jobs pay per year?

As of Sep 14, 2026, the average yearly pay for associate director gmp quality systems in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Associate Director Gmp Quality Systems jobs?

For Associate Director Gmp Quality Systems jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Gmp Quality Systems job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Quality Systems Director

Edison, NJ • On-site

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Full-time

Re-posted 11 days ago

Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

The Director of Quality Systems is responsible for the Quality System  as they relate to Investigations, Training and Auditing of suppliers and third party manufacturers.  The Director must have sufficient experience in manufacturing pharmaceutical products and understand industry standards to appropriately evaluate practices and procedures and be very familiar with various types of manufacturing technologies including oral solid dose, oral liquid, topical and sterile pharmaceutical products.  The experience should include specific technologies such as wet granulation, fluid bed coating, high speed compression, encapsulation, tablet coating, and sterilization techniques such as steam, dry heat, filtration, Ethylene Oxide and Gamma Irradiation.  The qualified candidate has appropriate experience in dealing with Governmental officials within the FDA at the District and Center levels.  Additional areas of responsibility include evaluating staffing needs, establishing requirements as per GMP and European standards, budget, training, prioritizing and scheduling of team activities and reporting quality progress on a weekly basis to site management.  This position must assure all GMP systems are of the highest quality and meet all applicable standards.

ESSENTIAL JOB RESULTS

  •        Responsible for implementing and maintaining a compliant Quality System per FDA and ISO requirements
    •        Oversee these quality systems within Novel: manufacturing, GMP documentation, quality records management, Validation, change control, calibration, labeling & packaging, product assessment and disposition, warehouse and distribution.
    •        Provides assurance that SOPs and practices within the manufacturing, testing, holding and distribution areas are adhered to and are appropriately maintained
    •        Responsible for assuring compliance of products manufactured in Novel's plant in Somerset.
    •        Assure GMP requirements are met and appropriate documentation is maintained
    •        Promote organization's growth and adherence to industry standards
    •        Ensures all company procedures, policies and systems are in accordance to industry regulations.
    •        Direct the development and implementation of departmental goals and objectives.
    •        Reporting on the performance of the quality system to corporate representatives and internal management.
  •        Coordinates, prepares, participates & responds to FDA, Foreign regulatory agencies and third party inspections.

REQUIRMENTS

Education

Minimum Bachelor Degree in a scientific or technical field; graduate degree desired.

Experience:

  •     9+ years' experience in a Quality and/or Regulatory management position in pharmaceutical manufacturing, preferably with some experience in aseptic processing.
  •     Working knowledge of FDA and applicable non-US regulations pertaining to pharmaceutical drug manufacturing
  •     Excellent managerial skills; includes project management, problem-solving, written and verbal communications, and organizational abilities
  •     Excellent teamwork, leadership, influencing, and coordinative skills; must be able to work with diverse teams to achieve results
  •     The ability to train employees, develop junior managers, and raise process improvement skills and overall quality standards across multiple functions
Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.
Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

View All Integrated Resources Jobs

Apply