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Careers at Siora Surgicals

At Siora Surgicals Pvt. Ltd we’re working every day to meet or even exceed our goal of becoming the healthcare provider of choice. We dedicate ourselves to the highest level of employees care. Each day brings new discoveries and new challenges.

We feel proud of us for supportive working culture, and the great opportunities we offer to our employees for training and advancement.

As an employee at Siora Surgicals,

  • Meet amazing and inspiring people every day.
  • Develop your existing skills while discovering new ones.
  • Find meaning in every workday.

We welcome ambitious, skilled, experienced professionals to join our team and grow with us by proving their mettle. You can send your resume per email with the remark “FOR HR Department” We will love to contact you if we have the right position available for you.

  • Admin
  • International Marketing
  • Domestic
  • Digital Marketing
  • Accounts
  • Design & Development Department
  • Production
  • Quality Control
  • Regulatory Affairs

Current Openings

We are presently looking for: -

Regulatory Affairs Executive

Number of Openings: 01

Job Description: Preparation of documentation for submission to FDA for medical device approval and/or response to FDA inquiries

Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017.

Experience: Minimum 02 Years

Salary: 20K -25K

Industry: Medical Devices/ Equipment

Functional Area: Legal, Regulatory

Employment Type: Permanent Job, Full Time

Job Location: Plot No. 1792, HSIIDC, Industrial Estate, Rai, District – Sonipat, Haryana.
Key skills:

Thorough knowledge of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017

Desired Candidate Profile

Minimum B. Tech in Mechanical, Bio Medical, B. Pharma, B. Tech Bio Medical Science or a science discipline

  • 2+ years of experience implementing test strategies, test plans and test cases for validation and verification in FDA-compliant medical device industry
  • Demonstrated success in a start-up, entrepreneurial work environment
  • Thorough knowledge of FDA Quality System requirements, ISO 13485:2012 (Quality System) requirements, ISO 14971 (Risk Management) requirements, Medical Device Directives (MDD) requirements, Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards
  • 2+ years of experience in verification/validation of products incorporating scalable data acquisition, processing, management, and reporting functionalities.
  • 2 or more years of experience with QMS implementation that complies with, MDD /93/42/EEC, ISO 13485 and ISO 14971 standards.
  • Lead role (administrative or technical) in one or more FDA submissions for approval of a medical device
  • Project management skills and proficiency and analysing and interpreting test data

Education-

UG: B Tech in Mechanical, Bio Medical, B. Pharma, B. Tech Medical Science or a Science Discipline

Company Profile:

One of the leading manufacturers and suppliers of Orthopedic Implants and instruments, founded in 1987 and having manufacturing unit at Rai Industrial Area, District Sonipat, Haryana and Corporate Office in Phool Bagh, Rampura, New Delhi Near Ashok Park Main Metro Station.

Note: Kindly mail your resume to hr@siora.net. Our HR team will call you for the interview if your resume is selected.

Quality Assurance Executive

Number of Openings: 02

Job Description:

  • Create and maintain company quality documentation, such as manuals, procedures, etc.
  • Continuously improve QA processes and procedures.
  • Preparation of QA reports.
  • Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012

Experience: 00- 02 Years

Salary: 15K -20K

Industry: Medical Devices/ Equipment

Functional Area: Quality Assurance

Employment Type: Permanent Job, Full Time

Job Location: Plot No. 1792, HSIIDC, Industrial Estate, Rai, District – Sonipat, Haryana.
Key skills:
Thorough knowledge of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017

Desired Candidate Profile

  • Implementation and improvement in Quality Management System as per ISO 13485:2016.
  • Implementation & Formation of Standard Operating Procedure (SOP) & Protocols as per GMP.
  • Maintain complete documents of various departments like Site Master File, Device Master File with easy archival/retrieval.
  • Involve onsite into the calibration & Validation activities. Preparation of Calibration calendar and preventive maintenance.
  • Assist in preparation of Batch Manufacturing Record as per manufacturing and their review before release of the batch.
  • Giving line clearance before starting the New Batch.
  • Review and analysis of Environmental Monitoring plan to monitor environmental condition and hygiene of Personnel working in manufacturing areas and other controlled areas.
  • Experience of CE, ISO 13485:2016 and GMP Inspections.
  • Experience of Risk Management as per ISO 14971
  • Experience of Design & development file as per ISO 13485:2016
  • Knowledge of Post Market Surveillance and Post Market Clinical Follow Up, Product recall-Handling and handling market complaints as per SOP and maintaining its records.
    Education- UG: B Tech in Mechanical, BE - Bio Medical, B. Pharma, B. Tech Medical Science Implementation and improvement in Quality Management System as per ISO 13485:2016.

    Company Profile:

    One of the leading manufacturers and suppliers of Orthopedic Implants and instruments, founded in 1987 and having a manufacturing unit at Rai Industrial Area, District Sonipat, Haryana, and Corporate Office in Phool Bagh, Rampura, New Delhi Near Ashok Park Main Metro Station.

    Note: Kindly mail your resume at hr@siora.net. Our HR team will call you for the interview if your resume is selected.

Job Description: VMC/CNC Setter

Manual Setting on VMC/CNC Machine
Experience: Minimum 10 Years
Salary: 18K -20K
Industry: Medical Devices/ Equipment
Functional Area: Production
Employment Type: Permanent Job, Full Time
Job Location: Plot No. 1792, HSIIDC, Industrial Estate, Rai, District – Sonipat, Haryana.

Key skills:

Candidate should have sound knowledge of Manual Programming on VMC/CNC Machine and should be experienced in VMC/ CNC Machine Setting.

Desired Candidate Profile
Candidate with sound knowledge of VMC/CNC Setting.

Education-

I T I Trained, Mechanical Diploma

Senior Design Engineer

Number of Openings: 01

  • Working on Solid Works / Solid Cam with Sound Knowledge
  • Software Programming to Practical Machine Implementation
  • Programming of 3 Axis VMC, 5 Axis VMC Sliding Head Automatic Lathe
  • Making of 2-D Drawing
  • Making of 3-D Models & Drafting
  • Modification of All Drawings
  • Making of Process Drawing
  • Making of Process Flow Chart
  • All Documentation Work As – Design Dossier, Master Drawing File
  • Making of Prototype & Master Drawing

    Experience: Minimum 10 Years’ Experience
    Salary: 50K
    Industry: Medical Devices/ Equipment
    Functional Area: Design & Development
    Employment Type: Permanent Job, Full Time
    Job Location: Plot No. 1792, HSIIDC, Industrial Estate, Rai, District – Sonipat, Haryana.
    Education:- B.Tech / Diploma in Mechanical with Solid Works / Solid CAM

    Desired Candidate Profile

  • Sound Experience in Solid CAM / Solid Works
  • Must be able to fully interpret Technical Drawings, Blueprints, Specification, and Illustrations.
  • Should have experience in an engineering/manufacturing environment with mechanical or tool design.
  • Understanding of Dimensioning, Geometric Tolerance, and Solid CAM / Solid Works Principles

    Note: Kindly mail your resume to hr@siora.net. Our HR team will call you for the interview if your resume is selected.

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