Primary Purpose and Overall Objective of the Job:

The PCR Specialist II is responsible for the formulation of highly complex PCR products and sub-solutions within the required timeframes and production schedules, in compliance with established Safety and Quality standards. They will be responsible for the proper handling and accurate pipetting of numerous different raw materials, combining 5-15 components into a final chemical formulation. Additionally, they will be responsible for the proper dispensing and labeling into final, customer facing formats. 

Main Accountabilities:
Participate in the manufacture and assembly of PCR Commercial Products, including final PCR products and sub-solution preparations via laboratory benchwork
Perform chemical titrations to a variety of raw materials and calculate and analyze data to prepare them in production ready formats
Working with supervisor, present continuous improvement opportunities through team and individual initiatives
Contribute to team goal development, tracking status and communicating with leadership team
Utilize a variety of software systems to support and track daily work activities (i.e. Microsoft Excel, Netsuite ERP, Dropbox, Tulip, etc.)
Ensure the Manufacturing batch records and other documentation are prepared, completed and stored at the highest standards according to company policy
Assist with the development, implementation, and support of manufacturing automation with collaboration from stakeholders and impacted departments
Comply with safety requirements, cGMP, SOP and manufacturing documentation
Prepare, fill, label and package solutions for the production and distribution
Execution of critical and routine and non-routine production operations
Record data and update inventory into database
Plan and conduct troubleshooting and corrective actions for unusual events or discrepant results

Typical Studies-Experience, Skills and Qualifications:
Studies-Experience
Bachelor’s degree in biology or related field and between 1 to 3 years of industry experience or equivalent experience in GMP related industry
Skills and Qualifications:
Proficiency in liquid handling, specifically pipetting and/or using automated liquid handlers
Working knowledge of Microsoft Office tools – Excel, Word and Outlook
Able to comprehend and complete moderately complex instructions, calculations and procedures