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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: -

CLINICAL RESEARCH ASSOCIATE

Experience: Minimum 02 Years
Industry: Medical Devices/ Equipment
Functional Area: Regulatory
Employment Type: Permanent Job, Full Time
Job Location: Plot No. 1792, HSIIDC, Industrial Estate, Rai, District – Sonipat, Haryana.

Desired Candidate Profile
Minimum B. Tech in Bio-Medical/ Bio-Tech or any Science discipline related to Human Anatomy & Physiology
Key skills:

  • Medical writing experience in the medical device industry or academia
  • Experience within clinical research, regulatory, quality, or product support/R&D
  • Experience in clinical research methodology, tools, processes and regulations
  • Experience writing Clinical Evaluation Reports (CERs) and related clinical regulatory documents.
    Competencies:

  • Experience performing literature searches in PubMed and other relevant platforms, literature identification and analysis
  • Ability to critically analyze and interpret scientific data (clinical and preclinical)
  • Ability to coordinate and prioritize multiple projects simultaneously
  • Ability to build and foster relationships with key business stakeholders/ distributors and cross-functional team members, doctors and other relevant person;
  • Strong attention to detail; ability to find and correct errors in spelling, punctuation, grammar, consistency, clarity and accuracy
  • Self-motivated team player
  • Highly motivated and capable of comprehending large amounts of scientific content, which is then communicated in a clear, concise fashion
  • Working knowledge of regulatory guidance relative to Clinical Evaluation Reports and the essential requirements for safety and performance of Medical Devices as defined in Annex I of the Medical Device Directive 93/42/EEC and he MEDDEV and EN ISO 14155 and EU Medical Device Regulation, ISO 13485:2016

    Proficient in Microsoft Office Suite software, Adobe software, net browsing and other relevant software.

    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.

  • Regulatory Affairs Executive

    Number of Openings: 01

    Job Description: The 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.
    • The 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

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