Posted to MedZilla on 9/23/2017


Takeda Pharmaceuticals

US-MN, QC Analyst I 1702098-MZ


 
 

QC Analyst I
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Quality Control Analyst I in our Brooklyn Park, Minnesota office.
Takeda is a global, innovation-driven pharmaceutical leader with 30,000 professionals working together across more than 70 countries. We have an unwavering dedication to put patients first for more than 230 years while we live our values of Takeda-ism Integrity, Fairness, Honesty, and Perseverance. We are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine.
Here, everyone matter and you will be a vital contributor to our inspiring, bold mission. As a Quality Control Analyst I working on the Quality team, you will be empowered to use your analytical skills and scientific background to maintain product quality, and a typical day will include:

POSITION OBJECTIVES:

  • Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers.
  • Conduct critical biological test methods including samples generated for in-process, drug substance and stability.
  • Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS).
  • Follow SOPs to perform methods requiring precise analytical skills and understanding of biology and chemistry principles.

POSITION ACCOUNTABILITIES:

  • Demonstrate a functional understanding of a laboratory setting and Standard Operating Procedures (SOPs).
  • Complete all testing, including special project / protocol testing in a timely and appropriate manner.
  • Maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.
  • Exercise judgment within defined Quality Control procedures and practices to determine appropriate action.
  • Initiate low severity level deviations, CAPAs and change controls within the electronic Quality Management System.
  • Occasionally participate in functional efforts involving teams to solve problems of moderate scope where analysis of situations or data requires a review of identifiable factors.
  • Author minor revisions to existing SOPs.
  • Receives general instructions on routine work and detailed instructions on new assignments.
  • May be required to work overtime or be assigned to a different shift as needed.
  • May perform equipment maintenance and calibrations as required.

REQUIRED QUALIFICATIONS:

Bachelor s or Master s Degree in any Life Sciences with relevant laboratory coursework and 0-3 years of relevant experience.

  • Previous experience in a regulated environment desirable.
  • Ability to handle multiple tasks concurrently, and in a timely fashion.
  • Must have basic understanding of laboratory instrumentation.
  • Must be able to communicate effectively with supervisors and peers.
  • Must be able to read, write and converse in English.
  • Must be computer literate. Able to navigate, conduct searches, and complete online forms on Personal Computer for the purposes of training, performance management, and self service applications.
  • Good interpersonal skills and be able to work effectively and efficiently in a team environment.
  • Knowledge of cGMP manufacturing preferred.
  • Knowledge of basic chemical and biological safety procedures.
  • Must display eagerness to learn and continuously improve.
  • Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.

ANALYTICAL CHEMISTRY SKILLSET:

The familiarity or experience with the following assays:

  • SEC
  • CEX
  • Protein A HPLC
  • Oligosaccharide
  • Polysorbate 80
  • Karl Fischer
  • Appearance (Color, Clarity, Visible Particulates)
  • Concentration
  • pH
  • SDS-PAGE
  • CE-SDS
  • CE-LIF
  • IEF
  • icIEF
  • Particulate matter
  • Osmolality



PHYSICAL DEMANDS:

  • In general, the position requires a combination of sedentary work and standing for extended periods of time in the Quality Control labs.

TRAVEL REQUIREMENTS:

  • Willingness to travel to various meetings or training, this could include overnight trips.
  • Requires approximately 5% travel.

WHAT TAKEDA CAN OFFER YOU:

  • 401(k) with company match and Annual Retirement Contribution Plan
  • Tuition reimbursement
  • Company match of charitable contributions
  • Health & Wellness programs including onsite flu shots and health screenings
  • Generous time off for vacation and the option to purchase additional vacation days
  • Community Outreach Programs

Empowering Our People to Shine

takedajobs.com.

Takeda is an EEO employer of minorities, women, disabled, protected veterans, and considers qualified applicants with criminal histories in accordance with applicable laws. For more information, visit http://www.takeda.us/careers/EEO_Policy_Statement.aspx

No Phone Calls or Recruiters Please.

*LI-MJ1-USA


Schedule


Please visit our website at takedajobs.com

 
 


* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.