Laboratory Specialist

Dentsply

Ankara

İş Yerinde

İş Yerinde

25 gün önce yayınlandı

Job Type

Full-Time

Position Level

Specialist

Department

Quality

Quality

Application Count

181 application

Job Type

Full-Time

Position Level

Specialist

Application Count

181 application

Department

Quality

Kariyer Image

QUALIFICATIONS AND JOB DESCRIPTION

Wellspect is a global MedTech company active in the field of continence care. We support people suffering from urinary and bowel dysfunction by providing innovative solutions that enable people to live more independent and dignified lives. Our headquarters are based in Mölndal, Sweden. We have more than 1000 employees, operations in 18 countries, and distributors around the world.

Working at Wellspect

All Wellspecters are located in different parts of the world, and we have different backgrounds, responsibilities, and history with the company. But despite our diversity, we have one thing in common: We believe that the work we do really makes a difference to our users. Having that clear sense of purpose in our everyday work strongly contributes to our engaging organizational culture.

We are looking for a team member who would like to join our team in our Manufacturing Factory at Kahramankazan and continue shaping medical device production systems of tomorrow.

As Laboratory Specialist, you will be responsible for performing scientific testing on samples and reporting results under the guidance of Wellspect standard operating procedures and global policies. You will be directly reporting to Head of QA/RA.


Description of responsibilities:

• Perform and ensure the sterilization controls of sterile medical devices

• Perform the tests of sterile barrier systems

• Perform and report of microbiological tests for monitoring of clean room

• Testing and reporting of raw material analysis

• Follow-up of laboratory requirements

• Conduct data analysis of the results

• Continuously update of technical job knowledge by following Wellspect QA/RA training and learning opportunities

• Conduct documentation and inspection results by completing reports and logs on timely basis

• Support daily QARA tasks as needed

• Other duties as may reasonably requested from time to time by Head of QA/RA 


Required experience:

• Bachelor’s degree in Biology, Chemistry or Chemical Engineering from reputable universities preferably master’s degree in Microbiology

• Minimum 3 years laboratory experience in medical or pharma industry will be an asset


Required skills:

• Excellent command of written & spoken English 

• Good command of MS Office programs

• ERP knowledge is a significant plus

• Strong communication, negotiation, coordination, research, and analytical skills

• Ability to work alone or with minimal supervision. Individual must be detail oriented, well organized and able to focus on

• Good problem solving, planning and follow up abilities for a sustainable relationship with all stakeholders

• Teamwork oriented with multiple stakeholders

• No obstacle for travel 

• No military obligation for male candidates


 

Preferred Candidate

More than 3 years of experience
Bachelor’s(Graduate), Master’s(Graduate)
English(Reading : Advanced, Writing : Advanced, Speaking : Advanced)

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