7,160 Quality Control jobs in India

Position : Scientist Trainee Qualification : M.Sc. Analytical Chemistry / Organic Chemistry / General Chemistry Experience : Fresher Roles & Responsibility: :

Knowledge on chemistry / Analytical Chemistry

Will be involved in development of method / process / Research etc.

Should be able to interpret experimental data with the help of supervisor.

Has to record experiments in the lab record book.

Quality Control Engineer / Diploma or B.E. Civil fresher or experience

employment Type Full Time, Permanent

Role CateEducation

UG : B.Tech/B.E. in Mechanicalgory Production & Manufacturing

Experience : 0-5 years

salary : 12k - 25k

location ; Chennai TamilNadu

**Job Types**: Full-time, Regular / Permanent

Pay: ₹12,000.00 - ₹25,000.00 per month

Schedule:

- Day shift
- Morning shift

Ability to commute/relocate:

- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 1 year (preferred)

**Quality Control**

**Qualification**: Bsc, Msc, Bpharm, Mpharm, or any with similar Industry experience

**Experience **- 2 to 12 Yrs

**Location**:Hyderabad (Choutuppal)

**Industry**:Herbals/Nutraceuticals/ Pharma/Healthcare/FMCG

**Responsibilities**:
Quality Control involves the testing and monitoring of products and services to ensure that they meet the required quality standards. For example,
- Performing the analysis of In-process samples, Raw material samples, Re-test samples Finished product samples.
- Responsible for the Preparation of Standard Operating Procedures related to Quality Control department.
- Responsible for the preparation of Specifications and Method of analysis.
- Standardization of Control samples.

**We are hiring a Quality Control for our client.**

**Job**
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**Sector**: Automotive

**Job**
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**Type**: Permanent

**Working**:Office Only

**Location**: Thirumudivakkam,Chennai

**Experience**:1 - 5 Years

**Requirements**:
**Skills Required**:

- Knowledge in preparation of documents like PPAP, APQP, FMEA, CAPA, 8D,
- 5Why, Process, Product & Layout Audit, MSA, SPC,
- Part quality standard report, Final inspection report,
- control plan, 5S plan and 7QC tools

**Notice Period**: Join within 7 days

**Are you the perfect fit? Great - Please share your updated CV and we will get back to you as soon as possible**

Knowledge in preparation of documents like PPAP, APQP, FMEA, CAPA, 8D, 5Why, Process, Product & Layout Audit, MSA, SPC, Part quality standard report, Final inspection report, control plan, 5S plan and 7QC tools

Job Profile:
We are looking for Quality Control with 4+ years of experience in quality management with ability for attention to key areas and eagle eye analysis. The person/s must be efficient, task oriented and ready to take responsibilities with ability to learn and keep themselves updated with cutting edge tools and technologies. You’ll be enthusiastic with a positive attitude, dedication and willingness to work hard.

Key Responsibilities
- Ensuring implementation and maintenance of key standards and guidelines.
- Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams.
- Devising ways to improve the quality and ensure quality delivering of the projects.
- Devising, improving, and reviewing the processes and procedures for projects and training the team to use them.
- Ensuring legal obligations are followed and ensuring compliance with regulatory bodies and guidelines.
- Overseeing product development procedures to identify any deviations from quality standards.
- Inspecting the final output, comparing it to the requirements, and approving or rejecting the final product.
- Solicit feedback from clients to assess whether their requirements are met
- Keeping accurate documentation and performing statistical analysis.
- Gaining feedback from the clients, attending meetings, submitting reports and assisting external auditors and inspectors.
- Reporting back to top management on performance metrics and output data.

Key Skills
- 4+ years of experience in quality management
- In-depth knowledge of quality control procedures and relevant legal standards.
- Strong attention to detail, organizational, and leadership skills.
- Ability to summarize information and communicate effectively
- Project management and organizational skills.
- Excellent communication and listening skills.
- Broad knowledge of the company’s operation and its required QMS
- Certification of quality control is a strong advantage

**Salary**: ₹700,000.00 - ₹800,000.00 per year

Schedule:

- Day shift

Ability to commute/relocate:

- Kochi, Kerala: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 4 years (required)

Work Location: In person

Quality control

**Category**:Quality**Location**:Bangalore, Karnataka, IN- .**Department**: Global Legal Global Business Services (GL-GBS)-
**About the Department**
- Global Legal Global Business Services (GL-GBS) at Bangalore was established in 2011 and supports the Global legal organization across International Operations, North America Operations and Headquarters. The unit is anchored under Global Legal Operations and responsible for delivering efficient offshoring legal services in high quality. Examples include end-to-end contract management, trademark portfolio management, promotional materials review, export controls screenings, system/process management, data management, and digitalization.**The Position**
- As a Quality Checker, your primary responsibility will be to review and ensure the accuracy, consistency, and compliance of legal contracts, contributing to the overall quality of our legal documentation. Along with this, you’ll also be responsible for the below mentioned tasks:
- Reviewing legal contracts for accuracy, completeness, and adherence to legal standards and Novo Nordisk guidelines.
- Conducting thorough proofreading to identify and rectify grammatical, typographical, and formatting errors.
- Collaborating with legal and business teams to address any discrepancies and ensure alignment with business requirements.
- Verifying the consistency of language, terms, and references throughout all contract documentation;
- Tracking and documenting changes, ensuring version control and maintaining accurate records of contract revisions;
- Participating in the development and maintenance of standardized contract templates to enhance efficiency and accuracy

**Qualifications**
- Master or bachelor’s in English, preference to Law degree.
- 2 to 5 years of experience in quality check of content.
- Understanding of contractual review, revise contracts, highlight errors, editing and proof reading.
- Exposure of working in a global company.
- Exposure to contract management tool would be preferred.
- High quality, accountability, business mindset, ability to work independently and in teams
- Excellent English language written and verbal communication skills
- Good presentations skills with a global mindset.

**Working at Novo Nordisk**
- Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us! Together, we go further. Together, we're life changing.**Contact**Deadline**
- 30th Aug, 2024**Disclaimer**
- It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process_.- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Production

Msc / B.Pharm / M.Pharm

Assistant Manager

6-10 Years

sanad Ahemdavad

Pay: From ₹12,000.00 per month

Schedule:

- Day shift

**Experience**:

- total work: 1 year (preferred)

Work Location: In person

Application Deadline: 22/10/2024
Expected Start Date: 20/09/2024

**Quality control management Job work unit End to End.**
1.Raw materials quality review
2.Samples review.
3.Pre Production Meeting conduct and training
4.Inspections. Cut panel, online, finishing, ironing packing etc.,
5.Final Inspection
6.Person who will be based in and around Salem Preferred.
7.He should have prior experience in Quality checking in fabrics or têxtile industry.

Interview mode : Direct Face to Face Interview

Salary : 1 to 4.5LPA

Experience : 2 to 10 years

**Job Types**: Full-time, Permanent

Pay: ₹100,000.00 - ₹450,000.00 per year

**Benefits**:

- Food provided
- Health insurance
- Provident Fund

Schedule:

- Day shift

**Experience**:

- quality control in Textile industry: 1 year (preferred)

Work Location: In person