Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description 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 7years 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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Job Description 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 7years 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr