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Analyst 2, Compliance

Employer
BioMarin Pharmaceutical Inc.
Location
Novato, California
Start date
Oct 3, 2024
View more categoriesView less categories
Discipline
Regulatory, Legal/Compliance
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Biotech Bay, Best Places to Work

Job Details

Who We Are

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. 

Compliance Analyst 2   SUMMARY The Compliance Analyst 2 serves as an integral member of the Maintenance Operations team. This position is responsible for ensuring all facilities operations meet regulatory compliance standards. The Compliance Analyst 2 will play a crucial role in maintaining a compliant, safe, and efficient work environment while adhering to GMP and FDA industry regulations.    The ideal candidate will have experience working in a cGMP environment with experience in compliance, maintenance processes, change control, data analysis, investigations, and data presentation. This position requires a detail-oriented individual with the ability to analyze complex changes and investigations, and who can work collaboratively with cross-functional teams to maintain optimal inventory levels and support the company’s operational goals.    RESPONSIBILITIES   
  • Investigate and complete quality records including deviations, child investigations, CAPAs, effectiveness checks, and impact assessments. 
  • Execute and manage change control activities for GxP facility operations. 
  • Review and analyze reports for critical temperature environments. 
  • Maintain and update compliance documentation, including SOPs, work instructions, effectiveness checks, and training materials.  
  • Prepare compliance reports and dashboards to track key performance indicators (KPIs).  
  • Conduct regular internal audits of maintenance inventory procedures and documentation to identify and mitigate compliance risks. 
  • Analyze data to support decision-making and provide insights on compliance and inventory management performance.  
  • Identify opportunities to enhance compliance and inventory management processes. 
  • Perform analysis on maintenance lubricants for environmental compliance.  
  • Assist and participate in data gathering and presentation for regulatory inspections. 
    EXPERIENCE   Required Skills: 
  • Must have 3-6 years of experience in a GMP regulated environment. 
  • Proficiency working in ERP systems such as SAP and Oracle  
  • Proficiency working in Veeva Quality Management System 
  • In-depth understanding of cGMP, FDA, and other regulatory requirements related to pharmaceutical manufacturing and inventory management. 
  • Proficiency in following procedures in controlled documents  
  • Proficiency in cause mapping such as 5 Why’s and Fishbone Diagram 
  • Proficiency in analyzing data and translating findings into actionable insights. 
  Desired Skills: 
  • Experience with data visualization tools such as Tableau and Power BI 
  • Experience with lean practices and the DMAIC model 
  • Experience with advanced cause tools such as FMEA and fault-tree analysis 
    EDUCATION 
  • Bachelor’s Degree required such as Biology, Engineering, or Chemistry  
  • A combination of technical, military, and/or equivalent experience can be used in lieu of degree. 
  • Work experience in heavily regulated industry is preferred 
  EQUIPMENT N/A   CONTACTS There will be extensive contact with staff in Maintenance, Engineering, Planning & Scheduling, and Manufacturing.    SHIFT DETAILS This position must be available during regular business hours, Monday through Friday, 8 hours a day.    ONSITE, REMOTE, OR FLEXIBLE This is a flexible style position, requiring 3 on-site days per week.    TRAVEL REQUIRED No travel is required for this position.  We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Company

Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.

Using our unparalleled expertise in genetics and molecular biology, we have developed eight important medicines for patients with significant unmet medical need. Our approved therapies treat achondroplasia, severe hemophilia A and several rare inherited and lysosomal storage diseases.

As we have looked to expand our impact, our approach to cutting-edge science has remained the same. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. Our work is deeply rooted in genetic insights, meaning we target the underlying genetic changes or proximal molecular mechanisms of disease.

With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.

Company info
Website
Location
San Rafael and Novato
California
United States

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