logo inner

Sr. Manager, Quality Training

4D Molecular TherapeuticsEmeryville, California, United StatesOnsite
This job is no longer open

Attention recruitment agencies:


All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.4DMT is a clinical-stage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines. We seek to unlock the full potential of gene therapy using our platform, Therapeutic Vector Evolution (TVE), which combines the power of directed evolution with our approximately one billion synthetic AAV capsid-derived sequences to invent evolved vectors for use in our products.

We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles. These profiles will allow us to treat a broad range of large market diseases, unlike most current genetic medicines that generally focus on rare or small market diseases.  Company Differentiators: •    Fully integrated clinical-phase company with internal manufacturing•    Demonstrated ability to move rapidly from idea to IND•    Five candidate products in the clinic and two declared pre-clinical programs•    Robust technology and IP foundation, including our TVE and manufacturing platforms•    Initial product safety and efficacy data substantiates the value of our platforms•    Opportunities to expand to other indications and modalities within genetic medicine4DMT is hiring a Sr.

Manager, Quality Training to manage 4DMT's Quality Training Program. The Sr. Manager, Quality Training will be responsible for driving user-focused strategies to ensure effective and compliant training is efficiently delivered enterprise-wide via 4DMT's Learning Management System. The Sr. Manager, Quality Training will be responsible for working with key stakeholders in the business to define training requirements and ensure 4DMT's training processes and LMS configuration are designed to optimally achieve these requirements. This role is also responsible for ensuring training program inspection readiness / inspection support, maintenance of training records, and coordination of periodic in-person GXP training activities.Reporting to the Sr. Director of QA and Compliance. This role can be in-person or hybrid.

RESPONSIBILITIES:  


  • Management of 4DMT's Quality Training Program = 100% of the time:
  • Define/update policies and procedures related to 4DMT’s Quality Training Program
  • Work with functional leaders across the business to ensure enterprise-wide, role-based training requirements are defined appropriately and implemented within the LMS
  • Provide direction/guidance on Learning Management System configuration and related processes to IT LMS system administrators
  • Ensure LMS is configured and administered effectively to manage course deployments, tracking, and reporting
  • Ensure LMS course assignments are accurate and appropriate through governance and partnerships with functions across 4DMT
  • Author, coordinate, and execute regularly scheduled GxP / quality onboarding training for new hires
  • Coordinate annual GMP and GCP refresher training for personnel supporting GMP and GCP activities respectively
  • Participate in cross-functional project teams to refine training and on-boarding processes
  • Manage training administration, communications, curricula endorsements, and reporting
  • Ensure consistent implementation of LMS assessment feature best practices and standards
  • Work with assigned areas/lines to plan and coordinate training sessions to support compliance
  • Ensure that compliance reporting and inspection readiness support is provided to customers
  • Track and support reporting of training compliance metrics
  • Manage archival of training records as needed
  • Support audits/inspections of the training program and serve as the training program Subject Matter Expert during regulatory inspections
  • Work with interdepartmental subject matter experts at all levels of the organization to plan, develop, and coordinate execution of GXP training programs / initiatives

QUALIFICATIONS:


Education: 

  • B.Sc. minimum

Experience: 

  • 5 - 8 years of experience in biotech / pharmaceutical industry, including a training-related role.
  • Demonstrated knowledge of adult learning principles, instructional design, and project management expertise.
  • Advanced business knowledge of Clinical Research, Development, and Manufacturing in the pharmaceutical industry.
  • Demonstrated ability to manage multiple, highly complex projects concurrently.
  • Prior experience in monitoring adherence to compliance-based training programs.
  • Demonstrated ability to influence and negotiate effectively and implement large-scale change.
  • Experience with Learning Management Systems (experience with ComplianceWire preferred)

Skills: 

  • Knowledge of LMS administration and processing
  • Excellent written and verbal communication skills
  • Strong organizational skills
  • Proficiency in Microsoft Office (Outlook, OneNote, Excel, Word, PowerPoint,), Adobe Acrobat, survey tools.
  • Knowledge of GCPs, GLPs and GMPs

Base salary compensation range is $132,000 - $155,000Please note: the base salary compensation range and actual salary offered to the final candidate depends on various factors: relevant work experience, skills, and years of experience4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This job is no longer open

Life at 4D Molecular Therapeutics

The mission of 4D Molecular Therapeutics is to design and develop transformative gene therapy products using our proprietary technology to create novel adeno-associated virus variants to be utilized as treatments for serious unmet medical conditions. Our products are unlocking the full potential of gene therapy to treat, and potentially cure, genetic diseases. A large number of patients and diseases, who previously were not treatable by gene therapy, will be addressable by 4D products. 4D has one of the deepest and most diverse product pipelines in the gene therapy field. Adeno-associated virus (AAV) vectors have emerged as a favored delivery vehicle for gene therapy in the human body. They can deliver the genes for therapeutic proteins to accessible tissues in the body and are generally considered safe. Several AAV gene therapy products are in late-stage clinical development, and one product is approved in the EU (Glybera, Uniqure). However, these first-generation AAV vectors have limited utility for the majority of diseases. Many of these common AAV were discovered as laboratory contaminants and monkey infections, for example; they have not been customized as targeted medicines. In contrast, 4D customized AAV vectors, and the products made from them, are designed to unlock the full potential of gene therapy. Through 4D's Therapeutic Vector Evolution, we are able to create customized vectors solutions to overcome the hurdles identified with first-generation AAV vectors. 4D is creating the ultimate gene therapy products to cure genetic diseases using new customized delivery vehicles (vectors) to shuttle genes into the cells in any organ in the body. This 4D library of vectors will soon include several for the liver, several for the brain, several for the heart, the eye, muscle, and so on. Doctors will be able to hand pick a vector for any patient based on the organ that is diseased.
Thrive Here & What We Value1. Collaborative and innovative work environment2. Emphasis on scientific excellence and innovation3. Focus on patient outcomes and improving lives through genetic medicine4. Opportunities for career growth and professional development5. Commitment to diversity, equity, and inclusion6. Robust technology and IP foundation, including TVE and manufacturing platforms7. Initial product safety and efficacy data substantiates platform value8. Rapid progression from idea to IND9. Expanding opportunities in genetic medicine indications and modalities10. Internal manufacturing capabilities
Your tracker settings

We use cookies and similar methods to recognize visitors and remember their preferences. We also use them to measure ad campaign effectiveness, target ads and analyze site traffic. To learn more about these methods, including how to disable them, view our Cookie Policy or Privacy Policy.

By tapping `Accept`, you consent to the use of these methods by us and third parties. You can always change your tracker preferences by visiting our Cookie Policy.

logo innerThatStartupJob
Discover the best startup and their job positions, all in one place.
Copyright © 2024