Associate Director, Quality Systems

Precision Point Staffing ™
CA, United States
Full-time

Overview :

We are seeking a Senior Manager or Associate Director of Quality Systems to oversee our Quality Systems and serve as the primary System Administrator for Veeva Quality Documents and Training applications.

This role will support the execution of GxP quality activities, including the creation and management of document change control processes via Veeva, standard operating procedures (SOPs), GxP record processing and archival, offsite record storage, and employee training through Veeva Training.

The individual will also support deviation, CAPA, and Change Control programs, manage our GxP vendor management program, oversee GxP computer systems, and generate quality metric reports.

Daily responsibilities will encompass document control, training, and Quality Management System (QMS) activities.

Key Responsibilities :

  • Maintain Quality Systems documentation within the Veeva eDMS.
  • Manage eDMS activities as needed.
  • Lead implementation efforts for new Veeva systems.
  • Maintain document trackers and indexes for GxP systems.
  • Collaborate with functional area representatives to develop, update, and maintain SOPs.
  • Process and archive GxP records efficiently.
  • Administer GxP training, manage the training matrix, and maintain employee training records in Veeva.
  • Provide general support for the overall Quality System.
  • Continuously improve the supplier qualification and evaluation program, including Quality Agreements.
  • Prepare quality status reports for management reviews.
  • Act as the primary contact for GxP computer system validation and change control.
  • Manage and organize documents for offsite storage.
  • Improve GxP document templates used throughout Veeva.

Qualifications :

  • Bachelor’s degree in Life Sciences or a related field, or a combination of education and experience.
  • Minimum of 5 years of experience with eDMS or eLMS in a pharmaceutical cGxP environment.
  • Experience with Veeva Vault (superuser or Veeva Business Admin); trained System Administrator preferred.
  • Proficiency in MS Office and general computer skills.
  • Experience working with and formatting a variety of file types.
  • 6 days ago
Related jobs
Promoted
VirtualVocations
Burbank, California

A company is looking for an Associate Director, GMP Quality Assurance. ...

Promoted
CSBio
Menlo Park, California

Work with Operations, Manufacturing, Quality Control, and Validation to establish, develop, communicate, and maintain a validation assessment plan for all GXP assets, buildings, systems, including laboratory instrumentation and systems. Quality Assurance in a pharmaceutical, medical device or drug m...

Promoted
Fate Therapeutics
San Diego, California

Fate Therapeutics is looking for an Associate Director or Senior Manager, Clinical Systems. Lead the Clinical Systems function, acting as a subject matter expert (SME) and system administrator for Clinical Operations systems. Accountable for partnering internally and externally to implement and main...

Promoted
Insmed Incorporated
San Diego, California

The Associate Director, Quality Assurance - Analytical,GMP has responsibility for the QA oversight of Insmed Gene Therapy (GTx) analytical laboratories, review and approval of GMP analytical records. Apply Quality Risk Management for key processes and systems. Will also provide QA support for GTx Qu...

Promoted
Gilead Sciences, Inc.
Foster City, California

Collaborates with other R&D Quality teams to ensure assigned functions, programs or vendors have timely and robust support for quality data/ analytics and reporting, quality documentation and training, quality technology and systems validation, and other related activities. Associate Director, R...

Promoted
Bio-Rad Laboratories, Inc
Hercules, California

The Associate Director Global Supplier Quality Management (SQM) has overall responsibility for the Global Supplier Quality Program. Oversees Supplier Quality team that investigates, analyzes, and resolves supplier quality problems through conducting audits and analyzing defect trends. The program is...

Promoted
FUJIFILM
Thousand Oaks, California

Associate Director, Quality Control Microbiology. The Associate Director of QC Microbiology will provide strategic, technical, and operational leadership for QC Microbiology related activities. The Associate Director will provide guidance to the continuous improvement of Environmental Monitoring tre...

Premier Nutrition
Emeryville, California

PNC is looking for an experienced leader ready to help us continue to build our Quality team as an Associate Director of Co-Manufacturing Quality. The person in this role will be responsible for overseeing the Food Safety and Quality at these sites, continuously improving our Quality System, and dri...

Jazz Pharmaceuticals
Remote Non Sales-USA, California, United States
Remote

Associate Director Occupational & Product Quality Toxicology. Jazz Product Quality Toxicology (PQT) is primarily responsible for providing robust, scientifically sound toxicological hazard and risk assessments to support product quality activities associated with the manufacturing and marketing of J...

FUJIFILM Holdings America Corporation
Thousand Oaks, California

The Director, Pharmaceutical Quality Systems will lead the Quality Systems, Validation, Compliance and Supplier Quality Teams ensuring implementation of a phased appropriate program. The Director, Pharmaceutical Quality Systems will lead the Quality Systems, Validation, Compliance and Supplier Quali...