Joshua Fernandez

Joshua Fernandez has a diverse work experience in the pharmaceutical industry. Joshua is currently working as the Sr. Director of GMP Quality Operations at BlueRock Therapeutics, starting in October 2022. Before that, they held the position of Sr. Director of Quality Assurance at Checkmate Pharmaceuticals from March 2022 to September 2022. Joshua also served as the Director of Quality Assurance at Checkmate Pharmaceuticals from August 2020 to March 2022.

Prior to their roles at Checkmate Pharmaceuticals, Joshua worked at Gilead Sciences as a Sr. Manager of Quality Assurance from October 2015 to August 2020. Joshua also gained experience at Takeda Oncology, where they held roles such as QC Manager I from June 2014 to October 2015, and QC Analyst III from January 2012 to June 2014.

Joshua's earlier experiences include working at Pfizer as a QC Scientist III from 2009 to 2011, and as a QC Scientist II from June 2008 to August 2011. Joshua started their career at Wyeth Biotech as a QC Scientist I from August 2005 to June 2008. Before that, they worked at Acambis as a QC Analyst 2 from July 2004 to August 2005, and as a QC Analyst 1 from June 2003 to July 2004.

Overall, Joshua Fernandez has a strong background in quality assurance and quality control, with a focus on GMP operations in the pharmaceutical industry.

Joshua Fernandez attended Syracuse University from 1999 to 2003 and earned a Bachelor of Science degree in Biochemistry.