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Manager, Quality Control
IRVINE CA 92604
Category: Pharmacist
  • Your pay will be discussed at your interview

Job code: lhw-e0-84949427

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Allergan

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  Job posted:   Fri Feb 23, 2018
  Distance to work:   ? miles
       
  2 Views, 0 Applications  
 
Manager, Quality Control

**Manager, Quality Control**


**Irvine, California, United States** at -jobs-matching/location-only


5 hours agoPost Date


177904Requisition #


Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceuticals and biologic products for patients around the world.


Allergan markets a portfolio of best-in-class products that provide novel treatments for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology, anti-infective and cardiovascular therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives.


Our success is powered by our world-class team's commitment to being Bold for Life. Together, we build bridges, power ideas, act fast and drive results for our customers and patients around the world by always doing what it is right.


**Join one of the world's fastest growing pharmaceutical companies!**


At Allergan you will have the opportunity to thrive in a fast-paced, strategic environment where bold, innovative thinking isn't just welcomed, it's encouraged. Across all functions, we relish the opportunity to help our people fulfill their potential. Our rapid growth strategy means plenty of opportunities to step into the spotlight.


**Position Description**


This position will be responsible for the management of the BLI QC group and all associated support functions, including contract laboratory activities, ensuring that all Microbiology, Chemical, Potency and Biochemical testing is performed according to FDA, Foreign MOH and Allergan requirements.


**Key Responsibilities:**


+ This individual will verify that the quality of drug substance product meets all Regulatory commitments, manage the product stability testing program, and manage all associated contract testing facilities.

+ The individual will collaborate with and effectively represent BLI Management and QC in meetings with internal and external partner groups.

+ This individual will represent QC during regulatory or internal inspections and responding to any observations.

+ The individual will be responsible to ensure appropriate training and development plans are in place for all employees in the QC group.

+ The individual will be responsible to ensure the QC departmental budgets and project expenditures are managed in manner which maximizes value to Allergan and meets the BMD budgeting targets.

+ The individual will be expected to champion, lead and participate in continuous improvement activities within the BLI facility, including method improvements/verifications/validations and transfers.


**Knowledge, Skills and Abilities:**


+ Demonstrated knowledge and experience with validating QC methods for protein analysis.

+ Working knowledge of regulatory compliance and Experience working in a GMP environment. Familiarity with process characterization and process validation is desired.

+ Demonstrated ability to manage, multi-task, delegate, and retain flexibility in a dynamic environment.

+ Well developed written and oral communication skills. Motivated to work in a team environment.

+ Consistently deliver on commitments and respond to customers' needs in a timely and courteous manner.

+ Demonstrated knowledge of the use of a continuous improvement methodology in a lab testing environment, desired but not essential.


**Minimum Requirements and Education:**


+ MS in Chemistry/Biochemistry or a related Biological Science field with 3+ years of relevant industrial experience or BS in Chemistry/Biochemistry or a related Biological Science field with 5+ years of relevant industrial experience.

+ 3-5 years of experience with people supervision working in a technical environment

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