Job Details

SourceAbled is looking for a Bioprocess Technician III for our Pharmaceutical Client. If you possess strong attention to detail, the ability to follow outlined processes and have prior experience in bioprocessing or manufacturing, this position may be a good match for you.You will provide process execution and equipment operational activities in support of cGMP (current Good Manufacturing Practices) clinical and /or commercial manufacturing.  You will advise management of issues and opportunities for continuous improvement. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your  knowledge and commitment, you will create a collaborative teaming environment for your colleagues.

Candidates with autism, neurodivergence and/or disabilities highly encouraged to apply.

How You Will Achieve It

• Contribute to completion of project milestones and organize own work to meet project task deadlines.
• Assess challenges to the schedule and re-directing activities as necessary to minimize impact to quality, compliance and timelines.
• Capable of detecting technical problems and assisting the appropriate colleagues for resolution.
• Perform routine production preparation tasks such as preparing production glassware and other equipment by operating industrial washers, autoclaves and dehydrogenation ovens, use calibrated scales to weigh out dry components and use graduates and flasks to measure liquids.
• Able to collect and assemble applicable, vital information for recommendations to Production Supervisors and/or Manufacturing Process Engineers to assist in troubleshooting and decision making.
• Organize daily functions and work in concert with Bioprocessing Technicians in executing operational aspects for Fermentation, Purification, and Conjugation processing in a compliant, safe and efficient manner to maintain production schedules.
• Understand basic principles, operational aspects of production equipment, automation control systems, processing requirements and any related procedural requirements.
• Develop best practices and share with other teams and sites.
• Conduct all activities that are in accordance with company policies and Standard Operating Procedures, Values, and global regulatory guidelines, environmental guidelines, as appropriate, etc.
• Perform laboratory activities such as performing sample dilutions, pH, and conductivity readings.
• Provide input and revise Standard Operating Procedures, batch records, forms or other {Current} Good Manufacturing Practices {part of GxP} related documents to support continuous improvement efforts, investigation corrective actions etc.
• Track and follow-up on departmental commitments, investigations, change controls, change control and general compliance initiatives.

Qualifications

Must-Have

• Attention to detail
• Critical thinking skills
• Ability to perform basic mathematical calculations and learn new processes
• Proactive in engagement with key stakeholders
• Excellent verbal and written communication skills
• Ability to efficiently use current computer packages including Excel, PowerPoint, MS Project and Word

Nice-to-Have

• Bachelor's Degree
• Demonstrated experience within the biopharmaceutical industry, including knowledge and experience with relevant biopharmaceutical unit operations and/or laboratory operations
• Demonstrated experience in Food and Drug Administration regulated industry
• Experience in a biopharmaceutical or pharmaceutical {Current} Good Manufacturing Practices
• Knowledge of operational aspects for Fermentation, Purification, and Chemistry processing

  
PHYSICAL/MENTAL REQUIREMENTS

Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

This position has multiple shifts and scheduing options but shift flexibility is required for most roles.