9 Manufacturing Companies jobs in Risca

Quality Control Warehouse Operative

Location:Stores based in Clevedon, North Somerset

Salary:(DOE)

Full-time, Permanent

Working Hours: (Monday to Friday, 08:00 – 17:00, with occasional overtime)

About the Role

We are seeking a reliable and motivated Quality Control Warehouse Operative to join our team. This dual-role position involves inspecting goods as they pass through manufacturing to despatch ready for delivery in a professional and timely manner, while also supporting warehouse operations such as loading, stock control, and general stores duties.

If you're a team player with a strong work ethic and a passion for delivering excellent service, we want to hear from you.

Key Responsibilities

Warehouse & Quality Control Duties

• Perform a quality checks on products passing through manufacture prior to delivery recording and reporting on any issues accordingly
• Load and unload vehicles safely and efficiently.
• Maintain a clean, organised, and safe working environment.
• Support general warehouse tasks such as picking, packing, and order prep.

What We’re Looking For

Essential:

• Physically fit and able to handle manual lifting
• Punctual, dependable, and self-motivated

Desirable but not essential:

• Forklift Truck Licence (Counterbalance/Reach)
• Previous warehouse or stores experience
• UPVC industry experience

What We Offer

• Competitive salary  (based on experience)
• 28 days holiday (including bank holidays)
• Company pension scheme
• Overtime opportunities
• Free on-site parking
• Company-issued PPE and uniform

Interested? Please apply with your latest CV.

INDLS 

• Design, implement, and refine comprehensive quality control plans and methodologies for manufacturing operations.
• Conduct rigorous inspections and testing of raw materials, in-process components, and finished products to ensure compliance with specifications and standards.
• Utilise statistical process control (SPC) techniques to monitor manufacturing processes and identify deviations.
• Perform root cause analysis (RCA) for quality issues and implement effective corrective and preventive actions (CAPA).
• Collaborate closely with production, engineering, and R&D teams to integrate quality considerations into product design and manufacturing processes.
• Develop and maintain detailed quality documentation, including inspection reports, test results, and quality audit findings.
• Train and mentor production staff on quality standards, procedures, and best practices.
• Stay updated with industry regulations, quality standards (e.g., ISO 9001), and emerging technologies in quality control.
• Lead internal quality audits and participate in external supplier audits.
• Contribute to continuous improvement initiatives aimed at enhancing product quality, process efficiency, and customer satisfaction.

• Bachelor's degree in Engineering (Mechanical, Manufacturing, or related field) or equivalent practical experience.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
• Strong understanding of quality management systems (QMS), statistical process control (SPC), and root cause analysis methodologies.
• Proficiency in using precision measuring instruments and testing equipment.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
• Experience with lean manufacturing principles and Six Sigma methodologies is a plus.
• Familiarity with relevant industry standards and certifications (e.g., ISO 9001).

At Etex, our purpose is to inspire new ways of living. We are an international leader in sustainable construction, driven by a passion for excellence, but it's our people that are our top priority. We connect, collaborate, and champion the well-being of our employees, forming partnerships and pioneering change in our ever-evolving industry.

At Etex, we seek to make a meaningful impact in the lives .

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• Develop, implement, and manage the company's quality control strategy and policies.
• Oversee all aspects of product quality, from incoming materials to final product inspection.
• Ensure compliance with IATF 16949 and other relevant automotive quality standards.
• Lead and mentor the remote quality control team, setting performance objectives and providing guidance.
• Establish and monitor key quality performance indicators (KPIs) and report on quality metrics.
• Implement statistical process control (SPC) techniques to monitor and improve manufacturing processes.
• Manage the non-conformance process, including root cause analysis and the implementation of corrective and preventive actions (CAPA).
• Collaborate with engineering and production teams to resolve quality issues and improve product design.
• Drive continuous improvement initiatives to enhance product quality and reduce manufacturing costs.
• Conduct internal audits and support external audits by customers and regulatory bodies.

• Bachelor's degree in Engineering (Mechanical, Manufacturing, Electrical) or a related field.
• Minimum of 8 years of experience in quality control or quality assurance, with at least 3 years in a management role within the automotive manufacturing industry.
• In-depth knowledge of IATF 16949 standards and quality management systems.
• Proficiency in statistical quality control tools and methodologies (SPC, Six Sigma, Lean Manufacturing).
• Experience with root cause analysis techniques (e.g., 8D, FMEA).
• Strong leadership, team management, and communication skills.
• Proven ability to drive continuous improvement and achieve quality objectives.
• Excellent analytical and problem-solving capabilities.
• Ability to work independently and manage a remote team effectively.

• Performing analytical testing on raw materials, intermediates, and finished pharmaceutical products using various techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Preparing reagents, standards, and samples for analysis.
• Operating and maintaining analytical instruments, including calibration and troubleshooting.
• Interpreting test results and comparing them against established specifications and regulatory guidelines.
• Documenting all testing procedures, results, and deviations in accordance with GMP and company SOPs.
• Investigating Out-of-Specification (OOS) results and contributing to root cause analysis.
• Participating in method validation and transfer activities.
• Maintaining a clean and organized laboratory environment.
• Ensuring compliance with all safety regulations and procedures.
• Assisting in the training and mentoring of junior laboratory personnel.
• Contributing to continuous improvement initiatives within the QC department.

• Perform a wide range of analytical tests on raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis, FT-IR, Karl Fischer titration).
• Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, USP, EP).
• Analyze and interpret complex analytical data, ensuring compliance with specifications and quality standards.
• Investigate out-of-specification (OOS) or out-of-trend (OOT) results, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Prepare and review analytical method validation reports, analytical test methods, and standard operating procedures (SOPs).
• Maintain laboratory equipment, ensuring proper calibration, maintenance, and qualification.
• Participate in internal and external audits, providing necessary documentation and support.
• Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure product quality and compliance.
• Stay current with the latest advancements in analytical techniques, instrumentation, and regulatory requirements.
• Mentor and train junior analysts, providing guidance and technical support.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 6 years of experience in pharmaceutical Quality Control, with a strong focus on analytical testing.
• Extensive hands-on experience with various analytical instrumentation (HPLC, GC, spectroscopy).
• Thorough understanding of GMP, ICH, USP, and EP guidelines.
• Proven experience in method development, validation, and transfer.
• Excellent analytical, problem-solving, and data interpretation skills.
• Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
• Ability to work independently with minimal supervision and manage time effectively in a remote environment.
• Proficiency in LIMS and other relevant software.
• Experience with stability testing programs is a plus.