7,983 Iso 9001 jobs in India

Job Title: ISO 9001 – Quality Trainee (Fresher)

Location: Gandhinagar, Gujarat

Experience: Fresher (0–1 Year)

Job Summary:

We are hiring a fresher to support our ISO 9001:2015 Quality Management System. The candidate will assist in documentation, audits, and QMS implementation across departments.

Key Responsibilities:

• Assist in maintaining ISO 9001:2015 documentation
• Support internal audits and CAPA tracking
• Coordinate with departments for QMS compliance
• Help in quality reports and data entry

Requirements:

• Graduate in Engineering/Science/Management
• Basic knowledge of ISO 9001 (preferred)
• Good communication & MS Office skills
• Eager to learn and grow in quality/compliance

Interested candidate send your resume on or

Contact us

Job Type: Full-time

Work Location: In person

Key Responsibilities:

● Assist in writing and executing manual test cases.

● Perform regression, smoke, and exploratory testing.

● Document test results and report bugs using tools like JIRA.

● Learn and assist in basic automation scripting.

● Collaborate with the QA team in daily Agile routines.

Requirements:

● Should have 3 years of experience as a QA

● Pursuing or completed B.Tech/MCA or a relevant qualification.

● Strong logical and analytical thinking.

● Basic understanding of software testing concepts.

● Familiarity with any programming/scripting language is a plus.

● Excellent communication skills and a willingness to learn.

Good to Have:

● Knowledge of tools like Postman, Selenium, or JIRA.

1) Quality Assurance (QA) Officer:

Number Of Vacancies - 2

Experience: 1–2 years in Quality Assurance / GMP environment

Qualification: B.Sc. / M.Sc. (Chemistry / Life Sciences or related field)

Job Responsibilities:

• Review and check data, documents, and records to ensure accuracy and compliance.
• Preparation, review, and implementation of Standard Operating Procedures (SOPs).
• Support in routine QA activities related to GMP compliance.
• Conduct internal checks for data integrity and documentation practices.
• Assist in handling deviations, change controls, and CAPA as per company guidelines.
• Coordinate with different departments to ensure adherence to QA policies.

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Requirements:

• 1–2 years of relevant experience in QA, documentation, SOP preparation, and data checking.
• Good knowledge of GMP regulations and compliance requirements.
• Strong attention to detail and ability to maintain data integrity.
• Excellent communication and teamwork skills.
• Candidates residing in Navi Mumbai will be given preference.

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What We Offer:

• Opportunity to work in a GMP-compliant pharmaceutical environment.
• Learning and career growth in QA processes and compliance.
• Supportive and collaborative work culture.

Note : Location: Navi Mumbai (Preference will be given to candidates residing in Navi Mumbai and Training will be provided by the experience senior members.

2) Analytical Scientist :

Number Of Vacancies - 2

Experience: Freshers

Qualification: M.Sc. (Chemistry) and B.pharm

Basic understanding of analytical chemistry and chromatography, especially HPLC techniques.

Exposure to finished product analysis or routine compliance in HPLC is a plus.

Basic computer skills (MS Office, Excel) and proficiency in documentation practices as per industry standards.

Good communication, negotiation, and coordination skills.

Job Types: Full-time, Permanent

Pay: ₹15, ₹25,000.00 per month

Benefits:

• Provident Fund

Work Location: In person

Qualification:

Bachelors or Masters in Biomedical Engineering and at least 2 years of experience in quality management system for medical device (ISO

Experience and skills

 A candidate should have hands on experience on implementing quality

management system ISO 13485.

Candidates must provide details of QMS projects handled.

nowledge of ISO and IEC standards such as ISO 13485, IEC 60601 standards

ualified internal auditor for ISO 13485

nowledge of Indian Medical device rule,2017.

undamental understanding of product development process (for new

product development) which includes knowledge of hardware, software,

mechanical and regulatory development activities amongst others

Roles and responsibilities

anage quality assurance procedure and records.

lan and guide various labs test for innovative medical device.

repare and submit device dossiers to regulatory bodies as per client needs.

lan and conduct internal audits. Participate in the corrective and preventive

action process.

mparting QMS training to new joinee.

dentifying regulatory design input for design team.

dentifying device related risk as per applicable regulatory requirements.

nsuring medical standard compliance - Studying the applicable product

standards for medical devices, analysis of all applicable sections,

documenting the requirements and design aspects based on the study.

Helping and tracking the implementation.

nsure design and test methodologies meets internal and external regulatory

requirements

xcellent understanding of product risk analysis and FMEA processes w.r.t

corresponding medical standards (IEC ,IEC , ISO 14971 etc).

etailed analysis of Software related risks and processes according to IEC

62304

etailed analysis of usability aspects of medical devices according to HFE 75,

IEC 62366, IEC , data security standards etc.

lan clinical trials for innovative medical device and corresponding regulatory

submission related processes and documentation

orking with cross functional teams to ensure compliance to medical

standards and applicable regulatory rules to ensure good quality project

deliverables.

onducting clinical literature search using databases such as PubMed,

and other internet sources to obtain relevant research

papers for the given medical device.

taying updated on recent trends, developments and advances in medical

device standards.

Add on skills

nowhow of FDA, CE and corresponding compliance requirements

xperience in IVD device, combinational medical device

nderstanding the requirements the quality system requirements of

Regulation MDR 2017/745 and IVDR 2017/746

Other skills

trong analytical skills

etail oriented approach to problems

trong reviewing skills

ood communication and presentation skills

ocus on achieving goals and delivering results

ollaborate and create alignment in a team environment