Are you looking for a job that will help you assist in ending the COVID-19 pandemic? We have partnered with an industry leading bio-pharmaceutical manufacture that is ramping up production for a Corona Virus vaccine. This Albuquerque, NM based sight is seeking to increase its headcount by 100 individuals over the course of the next year to keep up with production! As a part of the first wave of growth my client is seeking a talented Validation Analyst to join its rapidly expanding team.
The Validation Analyst will have the following responsibilities:
- Execute validation and qualification protocols for all validated equipment, utilities, systems or processes.
- Execute protocols for validations, documenting data for equipment, processes, utilities, systems and components.
- Understand and implement safety procedures and cGMP.
- Able to train other validation personnel in Validation Technician and Senior Technician duties.
- Reviewing reports and documents to ensure required information is complete and accurate.
- Participate in departmental level committees and Operational Excellence projects.
- Be aware of changes impacting internal SOPs and notifies management and coworkers of applicable changes.
- Keep up with pharmaceutical and regulatory publications.
- Under general supervision, reports data using well
The ideal candidate will have the following qualifications:
- At least 2 years of validation experience at sterile cGMP manufacturing facility.
- Experience with cleaning validation.
- Bachelors degree, but open to lower education achieved with additional work experience.
