Takeda Freshers Microbiology Quality Control Analyst – Apply Online
Takeda, id transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Job Title: Quality Control Analyst I – Microbiology
Location: Brooklyn Park, MN
What you bring to Takeda:
- Bachelor’s or Master’s Degree in any Life Sciences with relevant laboratory coursework.
- 0-3 years of relevant experience
- Previous experience in a regulated environment is 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 managers and peers.
- Must be able to read, write, and converse in English.
- Must have basic computer skills. General use of word processing, spreadsheets, databases, etc. for the purposes of work execution, training, performance management, and self-service.
- Good interpersonal skills and 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.
- Stand or sit -> Must be able to remain in a stationary or standing position for extended periods of time in both office and laboratory environment.
- In certain areas of Quality Control, the following may apply:
- Carry weight, lifting – Frequently moves laboratory materials and portable instruments weighing up to 30 pounds.
- Climb – Occasionally ascends/descends step ladders to reach materials and/or stairs to collect samples.
- Dexterity/balance – required to gown for cleanroom work, balance and dexterity are required.
- May be required to wear personal protective equipment (PPE) and other cleanroom garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full-body gowns, hair nets and gloves, and hearing protection.
- May be required to participate in an on-call rotation for off-shift coverage or occasionally work off-shift hours to help support a 24-7 manufacturing department.
- Willingness to travel to various meetings or training, this could include overnight trips.
- Requires approximately 5% travel.
What Takeda can offer you:
- Comprehensive Healthcare: Medical, Dental, and Vision
- Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan
- 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 and company match of charitable contributions
- Family Planning Support
- Professional training and development opportunities
- Tuition reimbursement
About the role:
- 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 and Empower).
- Follow SOPs to perform methods requiring precise analytical skills and understanding of biology and chemistry principles.
How you will contribute:
- Demonstrate a functional understanding of a laboratory setting and Standard Operating Procedures (SOPs).
- Work within laboratory environment for extended periods of time, conducting analytical tests, reviewing analytical data, maintaining laboratory materials and instruments, and other laboratory functions as required
- 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.
- Complete mandatory training within the required timeframe.
- Perform other duties as assigned.
Takeda Freshers Microbiology Quality
