About the Company
At Terumo Blood and Cell Technologies, our 7,000+ global associates are proud to come to work each day, knowing that what we do impacts the lives of patients around the world. We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient’s life every second of every day and are committed to continuing to increase the number of patients we serve. With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits, and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow, and be part of a team that is focused on making a difference. Consider joining our team and unlock your potential.
Job Title: Executive/Sr. Executive QC (Chemical/Functional/Component/Microbiology)
Company: Terumo Blood and Cell Technologies · Trivandrum, Kerala, India
JOB SUMMARY:
On-time completion of testing, analysis, and reporting with respect to regulatory guidelines.
ESSENTIAL DUTIES:
Administration/Internal Communications:
- Responsible for completing testing as part of Chemical, Functional, Microbiological and incoming inspection
- Responsible for providing support to Global Quality projects
- Responsible for providing support to complete gap assessments
- Other duties and responsibilities
Responsible for Analysis and inspection of raw materials, accessory items, and finished products. Responsible for In-process Testing and water testing. Responsible for Microbiological testing (Sterility/BET/Microbial Enumeration/Clean room monitoring). Responsible for making sure that data is accurately recorded in accordance with guidelines. Responsible for reporting, trending, and presenting results. Responsible for Calibration of Glassware and Instruments. Responsible for ensuring products are complying with the established regulatory guidelines with respect to product compliance. Responsible for ensuring GLP and cGDP requirements are in place. Responsible for supporting WCM, Lean, Six Sigma projects, root cause analysis, Productivity projects. Responsible for Maintenance of water quality through testing. Responsible for empowering people by giving required training. Responsible for qualification of analytical instruments and QC equipment. Responsible for New product evaluation and stability studies. Responsible for Monthly trending of test results. Responsible for subcontractor training and audits.
MINIMUM QUALIFICATION REQUIREMENTS:
Education:
Bachelor’s Degree in Pharmacy/ Master’s Degree in Pharmacy (Pharmaceutical Analysis/Pharmaceutics/Pharmaceutical Chemistry)
Experience:
2 to 8 year experience in relevant areas.
Technical Knowledge and Skills
- Knowledge of instrumental analysis (Ion chromatography/HPLC/UV/GC/FTIR etc)
- Knowledge of Microbiological testing
- Knowledge of performing tests as per Pharmacopoeial requirements (USP/IP/EP)
- Data Integrity
- Knowledge of different types of chemical analysis
- Able to understand and identify key objectives across the business
- Able to deal with multiple issues, tasks, and priorities concurrently
- Knowledge about blood bags and applications
Link to Original Notification to apply: Click here
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