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Senior Quality Control Manager - Automotive Manufacturing
                
    
    
            BN1 1AA East Sussex, South East    
                
         £60000 Annually 
    
                
    
                    
             WhatJobs
        
                    
    
        
                        
                                                Posted 19 days ago
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Job Description
Our client is seeking a highly experienced Senior Quality Control Manager to lead their quality assurance operations within a state-of-the-art manufacturing facility in **Brighton, East Sussex, UK**. This hands-on role is critical to maintaining the highest standards of product quality and ensuring customer satisfaction in a competitive automotive sector.
Key Responsibilities:
    Key Responsibilities:
- Develop, implement, and manage comprehensive quality control systems and procedures for automotive manufacturing.
- Oversee all aspects of the quality assurance process, from raw material inspection to finished product validation.
- Lead and mentor a team of quality inspectors, technicians, and engineers.
- Establish quality benchmarks, KPIs, and performance metrics to drive continuous improvement.
- Conduct regular audits of production processes and quality control measures to ensure compliance with industry standards (e.g., IATF 16949).
- Investigate quality issues, root cause analysis, and implement effective corrective and preventive actions (CAPA).
- Collaborate with R&D, engineering, and production teams to ensure product quality throughout the design and manufacturing lifecycle.
- Manage supplier quality assurance programs and conduct supplier audits.
- Ensure all quality control equipment is calibrated and maintained to the highest standards.
- Prepare detailed quality reports for senior management and stakeholders.
- Drive a culture of quality excellence throughout the organization.
- Stay current with advancements in quality management techniques and automotive industry best practices.
- Bachelor's degree in Engineering, Manufacturing, or a related technical field. A Master's degree is a plus.
- Minimum of 7 years of progressive experience in quality control and assurance, with at least 3 years in a management role within the automotive manufacturing industry.
- In-depth knowledge of quality management systems, such as IATF 16949, ISO 9001.
- Proven experience with quality tools and methodologies (e.g., Six Sigma, Lean Manufacturing, SPC, FMEA, APQP, PPAP).
- Strong understanding of manufacturing processes and common automotive components.
- Excellent leadership, team-building, and people management skills.
- Exceptional analytical, problem-solving, and decision-making abilities.
- Proficiency in quality reporting and data analysis.
- Strong communication and interpersonal skills, with the ability to collaborate effectively across departments.
- Experience with statistical software and quality control databases.
- Familiarity with metrology and inspection techniques.
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        Senior Pharmaceutical Quality Control Analyst (Remote)
                
    
    
            BN1 1UN East Sussex, South East    
                
         £55000 Annually 
    
                
    
                    
             WhatJobs
        
                    
    
        
                        
                                                Posted 20 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their dedicated remote team. This role is crucial for ensuring the quality, safety, and efficacy of our pharmaceutical products. As a remote analyst, you will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory techniques and instrumentation. You will meticulously document results, analyze data, troubleshoot analytical issues, and contribute to the maintenance of strict quality control standards in compliance with regulatory guidelines (e.g., GMP). This position requires a strong background in analytical chemistry, extensive experience with pharmaceutical testing, and the ability to work independently and effectively in a remote laboratory oversight capacity.
Key Responsibilities:
    Key Responsibilities:
- Perform a variety of analytical tests on pharmaceutical raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Develop, validate, and transfer analytical methods.
- Analyze test data, interpret results, and generate Certificates of Analysis (CoA).
- Troubleshoot and resolve analytical testing issues and equipment malfunctions.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Maintain accurate and detailed laboratory records and documentation.
- Participate in internal and external audits.
- Collaborate with R&D, production, and regulatory affairs departments to address quality issues.
- Contribute to continuous improvement initiatives within the Quality Control department.
- Stay current with advancements in analytical techniques and pharmaceutical quality control.
- A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
- A minimum of 5 years of experience in pharmaceutical quality control or a related analytical laboratory setting.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, KF, dissolution apparatus).
- Strong understanding of GMP, ICH guidelines, and pharmaceutical regulatory requirements.
- Proficiency in data analysis and interpretation, including statistical analysis.
- Excellent attention to detail and accuracy in executing test methods and documenting results.
- Strong problem-solving and critical-thinking skills.
- Effective communication and interpersonal skills for collaboration within a remote team.
- Experience with LIMS (Laboratory Information Management System) is advantageous.
- Ability to work independently and manage workload effectively in a remote setup.
- This position is fully remote , enabling you to contribute significantly to pharmaceutical quality from your home office. Our client is committed to fostering a high-achieving, collaborative remote work culture and offers excellent opportunities for professional growth.
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