Lead Biotechnologist (Downstream)

Purpose: 

• Performs functions associated with cGMP manufacturing operations within the biologics production facility including working with engineers in set-up and calibration tasks as well as performing rework and quality testing related to the production of parts components and final materials.  
• Completes batch documentation accurately and thoroughly while adhering to the required quality and safety standards and in a productive cost-effective manner. 
• Supports and leads operations & troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan.  
• Stands in as Deputy for Manufacturing Supervisor in his/her absence. 

Major Responsibilities:

• Plans and assigns daily production assignments to a team of Downstream biotechnologists.
• Operates with a high degree of technical expertise on the various purification processes: Chromatography Filtration Ultrafiltration Final Filling
• Demonstrates initiative to problem-solve with various cross functions (e.g. Technical Quality and Engineering)
• Coaches and trains junior biotechnologists in their area of work
• Ensures safe work environment in accordance with regulatory and global/local EHS policies
• Responsible for the completeness and accuracy of all records
• Ensures that all batch related document errors are resolved in a timely manner to avoid batch review and release delays
• Coordinates with various cross functions to provide windows for planned and unplanned downtimes.
• Drive performance to ensure execution is carried out flawlessly to ensure Human Error related events are prevented
• Responsible for overall plant upkeep
• Deputize in the absence of shift supervisor

Qualifications :

• Bachelors in Sciences (i.e. Biologicals Biomedical Chemistry Life Sciences Pharmaceutical) Pharmacy or Engineering (i.e. Biomedical Chemical Pharmaceutical) or equivalent 
• Min 7 years of relevant work experience in Biologics / Pharmaceutical industry is required.  
• Experience in leading a team is required 
• Good interpersonal and communication skills required 
• Excellent team player with experience in shift work preferred 
• Able to multi-tasks and work in a fast-paced environment preferred 
• Can work under pressure takes full ownership of tasks assigned and acts with personal integrity 
• Strong problem solving and prioritization skills are required 
• Knowledge of complex technical issues and manufacturing experience in a biopharmaceutical / pharmaceutical or similar environment 

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time