Responsibilities:

  • Understand customer needs and requirements to develop effective quality control processes
  • Devise and review specifications for products or processes
  • Set requirements for raw material or intermediate products for suppliers and monitor their compliance
  • Ensure adherence to health and safety guidelines as well as legal obligations
  • Supervise inspectors, technicians and other staff and provide guidance and feedback
  • Oversee all product development procedures to identify deviations from quality standards
  • Inspect final output and compare properties to requirements
  • Approve the right products or reject defectives
  • Keep accurate documentation and perform statistical analysis
  • Solicit feedback from customers to assess whether their requirements are met
  • Submit detailed reports to appropriate executives
  • Be on the lookout for opportunities for improvement and develop new efficient procedures
  • Knowledge of Production process of medical device manufacturing(IV Cannula)
  • Implementing and maintaining Quality Management System (QMS), that complies with ISO 13485, ISO 14971 and FDA 21 CFR Part 820,
  • Develop and implement quality control and inspection procedures for receipt and control of incoming materials, in-process materials and final product acceptance activities
  • Support the quality inspection to ensure , products and processes comply with the relevant requirements of the QMS
  • Analyze failure, corrective and preventive action to respond to internal/external customer complaints.
  • Manage, coordinate and oversee all validation studies, cleaning validation, change controls, protocol revisions, equipment validation, and documentation of results for manufacturing equipment’s
  • Data analysis, Continuously improve QA processes and procedures
    Establish and maintain test instrument calibration procedures and maintenance schedules
  • Data and record maintenance according to ISO 13485 certification
  • Responsible for conducting

Company Details

Company Name: Mediplus has been manufacturing I.V. Cannulas along with other medical products which has been caring and saving the human life from almost every ill effect medically. Mediplus India Ltd is in business since 1995 and has set a benchmark in its field. The major devices such as safety I.V. Cannula, I.V. Cannula, and Three way stop cock along with extension tubes are easily available in the market. Mediplus India LTD aims at providing the best medical disposable devices in the industry. We are constantly striving towards innovating and enhancing the technology that we use to manufacture our devices. Doing so helps us in creating a product that has a strong structure and a durable body. Our forward-thinking approach further deepens the trust of our customers in us.
Year of Establishment: 1994

Required Skills

Nature of Business: Full-Time
Sectoral Experience:
Performance Criteria:
Organisational Knowledge & Understanding:
Technical Knowledge: Excellent organizational, communication and leadership skills
Generic Skills: A keen eye for detail and a results driven approach
Professional Skills: In depth understanding of quality control procedures and relevant legal standards ,
Technical Skills: Excellent organizational, communication and leadership skills

Candidate Profile

Seniority Level: Entry Level
Min Qualification: Graduate
Max Qualification: Post Graduate
Specific Qualification / Degree required: BSc / Ba
Gender Preference: No Preference
Min Age Limit (in years): 23 year
Max Age Limit (in years): 40 year
Work Experience: 5 year
Language Proficiency Required for: Hindi, English

Remuneration & Benefits

Annual CTC from (in lakhs): 7.20
Annual CTC to (in lakhs): 8.40
Accommodation Benefits:
Meals Benefits:
Transport Benefits:
Incentives:
PF:
Mediclaim:
Insurance:
ESI:
Other Benefits:

Others

Work Timing / Shift Duration / Night Shift: Day Shift
Own Vehicle Required: No

Job Assessment

Assessment 00:10:00

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