Associate Director of Process Development and Documentation Job at Meet Life Sciences, Hayward, CA

dmlyQVFBRUpUUkFjRHdsMGE1bkVNcGI1SVE9PQ==
  • Meet Life Sciences
  • Hayward, CA

Job Description

Associate Director of Process Development and Documentation | Clinical Quality Assurance (CQA)

ONSITE SAN FRAN 3x PER WEEK - RELO PACKAGE OFFERED

Professional Summary: A highly experienced Clinical Quality Assurance professional with over 10 years of expertise in developing and maintaining clinical research SOPs, process development, and compliance for clinical-stage pharmaceutical companies. Proven leader with strong technical writing skills, capable of working cross-functionally to ensure adherence to industry standards and regulatory requirements. Experienced in managing audits, inspections, and continuous improvement of the Quality Management System (CQMS).

Key Skills & Expertise:

  • Process Development & Documentation: Expertise in developing and maintaining GCP, GLP, and GVP processes and SOPs. Adept at mapping and documenting clinical processes for clinical trials.
  • SOP Writing & Compliance: Strong experience in developing and reviewing SOPs, ensuring compliance with regulatory guidelines, and maintaining review timelines.
  • Inspection & Audit Support: Expertise in preparing for regulatory inspections (e.g., FDA, EMA) and supporting GCP, GLP, and GMP inspections. Experience in qualification audits of clinical service providers, investigator sites, and internal audits.
  • Non-Compliance & CAPA Management: Skilled in leading non-compliance event investigations and implementing corrective and preventive actions (CAPA). Focus on trends such as protocol deviations, safety, and other clinical data.
  • Leadership & Mentorship: Proven ability to lead cross-functional teams, mentor junior staff, and promote talent development within the Clinical Quality Assurance team.
  • Quality Metrics & Trend Analysis: Proficient in performing quality metric analysis to monitor clinical process deviations and CAPA effectiveness.
  • Industry Knowledge & Regulatory Trends: In-depth understanding of regulatory changes and industry trends related to clinical development and GCP, GLP, GVP compliance.

Professional Experience:

  • Led the development and documentation of GCP, GLP, and GVP SOPs, ensuring alignment with regulatory requirements and best industry practices.
  • Collaborated with Clinical Development teams to create and implement processes supporting clinical trials, focusing on quality assurance and compliance.
  • Managed cross-functional teams responsible for the creation and review of clinical SOPs and guidance documents.
  • Actively supported inspection readiness and prepared teams for regulatory inspections, ensuring compliance and mitigating risk.
  • Conducted audits of clinical documentation and service providers, including TMF and CSR reviews, ensuring adherence to SOPs and regulatory guidelines.
  • Led investigations into non-compliance events, developing and implementing CAPAs to address protocol deviations and safety issues.
  • Spearheaded the continuous improvement of the Quality Management System (CQMS), overseeing the creation and revision of SOPs and training programs.
  • Provided mentorship and development opportunities for junior team members, fostering a collaborative and growth-oriented environment.
  • Supported the development and implementation of GCP, GLP, and GVP SOPs, collaborating with clinical teams to ensure compliance with industry standards.
  • Led the preparation for regulatory inspections, ensuring clinical trial documentation met all regulatory agency requirements.
  • Performed quality metric analysis, identifying trends and ensuring corrective actions were implemented to improve compliance and reduce non-compliance events.
  • Assisted in the management and growth of the Clinical Quality Assurance team, contributing to team building, recruitment, and staff development.

Education:

Bachelor of Science (BS) in Biological Sciences (or related field)

Technical Skills:

  • Microsoft Office (Word, Excel, PowerPoint) : Advanced proficiency.
  • Process Development Tools : Experienced in using industry-standard tools for process mapping and documentation.

Job Tags

Similar Jobs

Medical Services of America

Certified Nursing Assistant - Hospice Job at Medical Services of America

 ...Albemarle Home Care & Hospice , a division of Medical Services of America, Inc., currently a full-time Certified Nursing Assistant for our patients in Elizabeth City (Dare, Currituck, Camden, Pasquotank, Perquimans, Chowan, Gates, and/or Bertie) NC. Job Description... 

Ledgent Technology

Technician - GMP Lab - Manufacturing Medical Equipment Job at Ledgent Technology

 ...Experience * Associate's Degree or equivalent or technical degree/certificate with 4 years previous experience in R&D Lab and/or medical device experience required, OR * 6 Years related experience required Required Skills * Strong written... 

Griffin Agency

Work from Home: Life & Health Insurance Opportunities Await! Job at Griffin Agency

 ...Who We Are : We are an insurance technology and distribution platform that is transforming the industry. We have developed a paperless...  ...than one minute. We are one of the top distributors of digital life insurance policies in the world. We have an in-house marketing... 

Attri

Technical Product Manager (AI Agent Platform) Job at Attri

 ...TechnicalProductManager,AI Location:Austin,TX(On-site) Compensation:Market-basedsalary plus performance-basedannualbonus WhyAttri AttriistheAIagentplatformthatturnsanybusinessideaintoaproduction-readyapplicationinminutesnotmonths... 

Pocketbook Agency

In-home Lifestyle Management and House Manager Job at Pocketbook Agency

 ...A high-net-worth family in Beverly Hills is seeking an experienced, detail-oriented In-Home Lifestyle Manager & House Manager to oversee the daily operations of their primary residence. The ideal candidate will be hands-on, polished, and proactive someone who thrives...