7 Tata Steel jobs in Corby

• Conduct inspections and tests on incoming materials, in-process production, and finished products.
• Verify that products meet established quality standards and specifications.
• Identify and document any defects or non-conformities.
• Perform visual inspections and use precision measuring instruments.
• Analyze test results and provide reports on product quality.
• Collaborate with production and engineering teams to address quality issues.
• Recommend and implement corrective actions to prevent recurrence of defects.
• Maintain accurate quality control records and documentation.
• Ensure compliance with quality management systems and industry standards.
• Participate in continuous improvement initiatives related to quality.

• Proven experience as a Quality Control Inspector or in a similar quality assurance role.
• Knowledge of quality control principles and methodologies.
• Experience with inspection tools and techniques.
• Ability to read and interpret technical drawings and specifications.
• Strong attention to detail and accuracy.
• Excellent analytical and problem-solving skills.
• Proficiency in MS Office Suite.
• Good communication and teamwork skills.
• High school diploma or equivalent; technical certifications are a plus.

We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.

Benefits:

• This is a full-time or part-time REMOTE position
• You’ll be able to choose which projects you want to work on
• You can work on your own schedule
• Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work

Responsibilities:

• Give AI chatbots diverse and complex chemistry problems and evaluate their outputs
• Evaluate the quality produced by AI models for correctness and performance

Qualifications:

• A current, in progress, or completed Masters and/or PhD is preferred but not required
• Fluency in English (native or bilingual level)
• Detail-oriented
• Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning

Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.

Benefits:

• This is a full-time or part-time REMOTE position
• You’ll be able to choose which projects you want to work on
• You can work on your own schedule
• Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work

Responsibilities:

• Give AI chatbots diverse and complex chemistry problems and evaluate their outputs
• Evaluate the quality produced by AI models for correctness and performance

Qualifications:

• A current, in progress, or completed Masters and/or PhD is preferred but not required
• Fluency in English (native or bilingual level)
• Detail-oriented
• Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning

Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

• Perform analytical testing of pharmaceutical materials using various instrumental techniques.
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Review and interpret analytical data, ensuring accuracy and compliance.
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results.
• Contribute to deviation investigations and the implementation of CAPAs.
• Ensure all laboratory activities comply with GMP, GDP, and other relevant regulations.
• Maintain and calibrate laboratory equipment, troubleshooting as needed.
• Prepare and review analytical documentation, including reports and validation protocols.
• Mentor and train junior laboratory personnel.
• Collaborate with cross-functional teams to resolve quality issues.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Significant experience in pharmaceutical Quality Control, with a focus on analytical testing.
• Proficiency in analytical techniques such as HPLC, GC, spectroscopy, and titrations.
• Thorough understanding of GMP, ICH guidelines, and regulatory requirements.
• Excellent documentation and data review skills.
• Strong problem-solving and critical thinking abilities.
• Effective communication and interpersonal skills.

• Perform qualitative and quantitative analyses of raw materials, intermediates, and finished products.
• Execute validated analytical methods using various laboratory instrumentation (e.g., HPLC, GC, UV-Vis, KF).
• Analyze and interpret test data, ensuring accuracy and completeness.
• Prepare and review analytical reports and certificates of analysis.
• Maintain laboratory equipment and ensure calibration and qualification.
• Ensure compliance with GLP, GMP, and other relevant regulatory standards.
• Document all laboratory activities meticulously in accordance with company SOPs.
• Troubleshoot analytical methods and equipment issues.
• Participate in method validation and transfer activities.
• Contribute to continuous improvement initiatives within the QC department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related field.
• Proven experience in pharmaceutical Quality Control or a similar laboratory role.
• Hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, etc.
• Strong understanding of GMP, GLP, and pharmaceutical regulations.
• Excellent data interpretation and report writing skills.
• Exceptional attention to detail and commitment to data integrity.
• Ability to work independently and manage workload effectively in a remote setting.
• Proficiency in laboratory information management systems (LIMS) and MS Office.
• Strong problem-solving and critical thinking abilities.
• Effective communication and interpersonal skills.

Astute People are working with a leading Waste Management Company who own & operate a number of Waste to Energy facilities across the UK. With two plants in Operation and a further two under construction, now is a great time to join the business as it grows. As part of their growth plans, they are looking for a Quality Control & Systems Co-Ordinator to join their QHSE Team.

As the Quality Control & Systems Coordinator you'll be responsible for the management and compliance of the Integrated Management Systems (IMS), policies and coordination and management of the SharePoint documentation system. This role will include site visits, key stakeholder meetings and technical understanding to manage the ISO certification across the fleet.

If you have a background in quality control, technical compliance or auditing and are looking to join a leader player in the Waste to Energy sector then apply for this role.

Responsibilities and duties of the Quality Control & Systems Coordinator role:
Reporting to the Head of Health, Safety & Compliance, you will be responsible for:

• Manage and Maintain Company Documentation: Oversee the control, accuracy, and accessibility of company documents within the Integrated Management System (IMS), including policies, procedures, and registers.
• Ensure Compliance with ISO Standards: Support and uphold compliance with ISO certification requirements by managing documentation and contributing to audit readiness.
• Review and Format Critical Documents: Review and quality-check new and revised documents to ensure they meet internal formatting standards and classification protocols.
• Maintain Document Management Systems: Proactively update and manage the structure and user interface of the company's SharePoint-based document management system, promoting consistency across departments.
• Monitor and Track Documentation Reviews: Maintain up-to-date registers and issue reminders to document owners ahead of review deadlines, ensuring timely updates and compliance.
• Conduct Document Audits and Report Findings: Perform regular audits at all levels, identify non-conformances, and follow up to ensure timely resolutions while documenting all corrective actions taken.

Professional qualifications
We are looking for someone with the following:

• Relevant qualifications in administration, quality or auditing
• Experience managing ISO compliance and standards
• Technical understanding relating to compliance within the Waste to Energy sector or similar Heavy Engineering sector
• This role will include infrequent travel to sites across the Midlands and North West so a full UK Driving Licence will be required

Personal skills
The Quality Control & Systems Coordinator role would suit someone who has:

• Excellent grasp of SharePoint and the MS Office Suite
• Thorough attention to detail
• Ability to deliver training on compliance needs
• Familiar with producing and presenting reports
• Project management experience

Salary and benefits of the Quality Control and Systems Coordinator role

• Industry competitive salary up to 50,000 (DOE)
• Bonus scheme
• Pension
• Further full company benefits

INDPOW

Astute People are acting as an employment agency in relation to this vacancy. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We encourage applications from individuals from all backgrounds but candidates must be able to demonstrate their ability to work in the UK. Astute is also committed to the government's Disability Confident Employer initiative. We endeavour to get back to everyone, however, if you have not heard anything after 7 days, please consider your application unsuccessful.