Danaher Pharma Analyst Job Opening – Quality Control
Pharma QA Analyst. Candidates with an M Pharma degree are encouraged and invited to apply online for an Application Specialist vacancy at Mumbai in Danaher. Check out all the details on the same below:
Job Title: Quality Control Analyst
Job Location: India-Karnataka-Bengaluru
GCRF Job Level: P1
GCRF Job Family: Quality and Regulatory Affairs
Eligibility:
Education and Experience:
• Master’s degree in Pharmacy), medical or technical field and 2+ years’ experience with increasing responsibility in Quality Control area
• Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable
• Quality competent technical person approved as per D&C act if any
Knowledge and skills:
- Hands on Experience on IVD product testing.
- Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS.
- Must be flexible to work off-shifts and weekends as per production Schedule.
- Schedule orientated (able to consistently maintains schedules and meet timelines)
- Strong interpersonal skills, Effective organization and Communication skills are essential.
- Good skills in English language
- Knowledge of Microsoft Word and Excel
- Strong multi-tasking and attention to details skills.
PREFERRED REQUIREMENTS:
• Experience working with medical device quality systems in compliance with MDR and ISO
13485• Able to interpret quality problem and establish practical solutions within a dynamic business environment.
• Experience in leading continuous improvement efforts, in both quality systems and products.
• Knowledge of the process of establishing facility QMS certifications.
• Cross functional experience with products and manufacturing processes to influence change at all levels within the organization
POSITION SUMMARY:
• Reporting directly to the head of India Quality System and Regulatory Compliance (QSRC) manager, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd.
• Ensure compliance of quality control procedures as per MDR 2017, European regulations, 21 CFR 820, ISO 13485, Cepheid corporate quality system requirements.
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I am working in APOTEX research pvt. As a senior technician in production development. My qualification is Diploma in pharmacy. 13 year of experience. I have good knowledge n work experience. Flexible to work.
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