13 Manufacturing Companies jobs in North Tyneside

The Company:

MTrec are currently recruiting for a renowned and respected company based in the Hetton Le Hole area. The role will be instrumental in supporting the company’s excellent quality standards, at all stages of the production process.

The role will be working a days and nights shift pattern, alternating on a two-week basis, from 07:00 and 15:00 and 23:00 to 07:00.

If you have previous quality experience and are looking for your next long term career move, apply now for an immediate response

The rewards and benefits on offer:

• Free parking onsite
li>Immediate starts available
• An opportunity within a growing and dynamic business
• Progression and development opportunities
• Ongoing training
• Competitive basic salary

The Job you will do:

• Prioritise Health & Safety, working within safe systems of work
• Perform QC testing of raw materials, intermediates, and finished goods
• Maintain accurate testing records and log deviations
• Calibrate and verify lab and production equipment
• Maintain certificates of analysis for lab equipment
• Identify and control non-conforming products, communicating issues to the wider team
• Coordinate external lab testing (microbiological, chemical, allergen), submitting samples and reporting any OOS results
• Create customer certificates of analysis
• Check product formulations and labels for accuracy
• Conduct regular site audits of processes, products, and personnel
• Take corrective actions for non-conformities identified in audits
• Monitor cleaning and hygiene standards to ensure product compliance
• Ensure all documentation is accurate, complete, and properly filed

About you:

• Experience in food manufacturing and BRCGS compliance is essential
• Background in Quality Control or Quality Assurance
• Knowledge of hygiene and technical standards
• HACCP knowledge
• QA auditing experience
• Fluent in English
• Computer literate

• Developing and implementing comprehensive quality control plans and procedures for all manufacturing processes.
• Conducting thorough inspections and testing of raw materials, in-process components, and finished products using various measurement and testing equipment.
• Interpreting technical drawings, specifications, and quality standards.
• Identifying non-conforming products, investigating root causes of defects, and implementing corrective and preventive actions (CAPA).
• Managing and calibrating quality control equipment to ensure accuracy and reliability.
• Maintaining accurate quality records, inspection reports, and statistical process control (SPC) data.
• Participating in internal and external audits to ensure compliance with quality management systems.
• Collaborating with production and engineering teams to resolve quality issues and implement process improvements.
• Mentoring and guiding junior quality control inspectors and technicians.
• Contributing to the development and continuous improvement of the company's quality management system (QMS).

• Performing a range of analytical tests on raw materials, in-process samples, and finished products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Preparing reagents, standards, and samples for analysis.
• Documenting all testing activities accurately and thoroughly in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Interpreting analytical data and reporting results.
• Troubleshooting analytical methods and instrumentation issues.
• Participating in method validation and transfer activities.
• Maintaining laboratory equipment and ensuring calibration is up-to-date.
• Contributing to quality improvement initiatives and CAPA investigations.

• Perform a wide range of analytical tests on pharmaceutical raw materials, intermediates, and finished products.
• Operate and maintain analytical instrumentation, including HPLC, GC, UV-Vis, FTIR, and others.
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Analyze test results, interpret data, and generate accurate reports.
• Investigate out-of-specification (OOS) results and deviations, and implement corrective actions.
• Ensure all laboratory activities comply with GMP, GLP, and relevant regulatory standards.
• Contribute to the continuous improvement of quality control processes and procedures.
• Collaborate with R&D, production, and regulatory affairs departments on quality-related issues.
• Maintain accurate and organized laboratory records and documentation.
• Participate in internal and external audits.

• Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific discipline.
• Proven experience as a Quality Control Analyst in the pharmaceutical industry.
• Strong knowledge of analytical techniques such as HPLC, GC, spectroscopy, and titration.
• Familiarity with GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
• Experience with method validation and development.
• Excellent data analysis, interpretation, and reporting skills.
• Meticulous attention to detail and commitment to accuracy.
• Proficiency in laboratory information management systems (LIMS) is desirable.
• Strong problem-solving and critical thinking abilities.
• Effective communication and teamwork skills.

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products.
• Develop, validate, and transfer analytical methods according to ICH guidelines.
• Operate and maintain sophisticated laboratory instrumentation (e.g., HPLC, GC, Spectrophotometers).
• Review and interpret analytical data, ensuring accuracy and compliance with specifications.
• Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results.
• Prepare and review Certificates of Analysis (CoA) and technical reports.
• Ensure laboratory operations comply with cGMP, FDA, and other regulatory requirements.
• Mentor and train junior QC laboratory personnel.
• Participate in laboratory equipment calibration, qualification, and maintenance programs.
• Contribute to the continuous improvement of quality control processes and procedures.

• MSc or PhD in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with HPLC, GC, and other relevant analytical techniques.
• Thorough knowledge of pharmacopeias (USP, EP, JP) and regulatory guidelines (ICH, cGMP).
• Proven ability to develop and validate analytical methods.
• Strong understanding of data integrity and documentation practices.
• Excellent analytical, problem-solving, and critical thinking skills.
• Superior attention to detail and organizational abilities.
• Effective written and verbal communication skills.

Rewards and Benefits on Offer;

• Temp to Perm Opportunities available after a 6-month probation period
• Identified Manufacturing Career Path for progression including Industry lead training and development
• Leading Pay rates including higher overtime rates
• A well-regarded company culture
• Free on-site parking
• Excellent transportation links
• Recommend a Friend £50 gift voucher
• Christmas events and vouchers

The P.

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MTrec are currently recruiting for a renowned and respected manufacturing company based in the Houghton area.
MTrec are currently looking for proactive individuals who are looking for a long term position in production and assembly.

The Job You'll Do:

• Assemble electronic circuit boards and perform soldering tasks in line with production drawings
• Inspect and test PCB assemblies and final products to.

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Rewards and Benefits on Offer;

• A highly varied and interesting role, working in a fast-paced environment.
• Employer pension scheme.
• Free onsite parking.

The Hours Youll Work;

• Continental Shift pattern
• 2 x 12 hour day shift followed by 2 x 12 hour night shift then 4 days off
• 07.00am till 19.00pm

The Pay Youll Receive;

• £15.92 per hour

MTrecs New Opportunity;

• MTrec are currently recruiting for a well-establ.

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