What Jobs are available for Quality Control in Rutherglen?

• Develop, validate, and implement analytical test methods for quality control.
• Perform complex chemical analyses on raw materials, intermediates, and finished products.
• Interpret analytical data and generate detailed quality control reports.
• Troubleshoot analytical instrumentation and resolve laboratory issues.
• Ensure all quality control activities comply with regulatory standards (e.g., ISO, GMP).
• Collaborate with R&D and production teams to address quality concerns.
• Maintain laboratory records and documentation in accordance with company procedures.
• Mentor and guide junior QC chemists.
• Contribute to the continuous improvement of quality management systems.

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, or a related scientific discipline.
• Minimum of 5 years of experience in a Quality Control laboratory role.
• Expertise in analytical techniques such as HPLC, GC, Spectroscopy, and Titration.
• Experience with method development and validation.
• Strong understanding of GMP, GLP, and relevant industry standards.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in laboratory information management systems (LIMS) is a plus.
• Strong written and verbal communication skills.
• Ability to work independently in a remote setting.

• Reviewing and analyzing raw data from various analytical techniques (e.g., HPLC, GC, spectroscopy) for pharmaceutical products.
• Ensuring all quality control testing is performed in accordance with approved protocols and regulatory requirements.
• Assessing batch release documentation for accuracy and completeness.
• Investigating deviations and out-of-specification (OOS) results, contributing to root cause analysis.
• Participating in the development and validation of analytical methods.
• Ensuring compliance with Good Manufacturing Practices (GMP) and other relevant quality standards.
• Authoring and reviewing quality control reports and documentation.
• Collaborating remotely with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs.
• Maintaining up-to-date knowledge of regulatory guidelines and industry best practices.

• Conduct comprehensive quality inspections of raw materials, in-process components, and finished goods.
• Utilize precision measuring instruments (calipers, micrometers, gauges) and CMMs.
• Interpret engineering drawings, specifications, and quality standards.
• Identify, document, and report non-conforming products and process deviations.
• Collaborate with production and engineering teams to resolve quality issues.
• Implement and monitor corrective and preventive actions (CAPA).
• Analyze quality data and trends to identify areas for improvement.
• Participate in internal and external quality audits.
• Develop and maintain inspection procedures and work instructions.
• Train and mentor junior quality control personnel.

• Proven experience as a Quality Control Inspector in a manufacturing environment, preferably automotive.
• In-depth knowledge of quality management systems (ISO 9001, IATF 16949).
• Proficiency in using various metrology and inspection equipment, including CMMs.
• Ability to read and interpret technical drawings and blueprints.
• Strong analytical and problem-solving skills with a keen eye for detail.
• Excellent communication and teamwork abilities.
• Relevant technical certification or apprenticeship is highly desirable.
• Experience with statistical process control (SPC) is a plus.

About the Role

We are seeking a strategic and hands-on Quality Manager to drive quality excellence across our European packaging operations. In this high-impact role, you’ll lead quality initiatives, manage supplier standards, and support client-facing activities to ensure our products consistently exceed expectations. The ability to successfully manage stakeholders during the change process in establishing quality processes is key.

Location: Flexible within Scotland (with intensive travel in the UK, EU & Asia, approx. 60% of the time)

Key Responsibilities

• Act as the regional quality expert for all EU business units and client projects.
• QA champion, educating all stakeholders and establishing QA processes within the organization.
• Represent the company in client audits and QA matters to build confidence and support sales.
• Build and scale a robust QA framework and team to support growth.
• Define and enforce quality standards for NPD and outsourced manufacturing (including China partners).
• Drive continuous improvement across processes and supplier quality.
• Oversee supplier auditing, performance monitoring, and compliance (FSC, ISO, BRC, SEDEX).
• Manage non-conformance reports (NCRs) and ensure issues are resolved effectively.
• Support sustainability, sourcing, and operational projects, including production relocation.

What We’re Looking For

• 5+ years of experience in QA/Quality Management (preferably in packaging or FMCG).
• Proven track record in managing global supply chains and client QA expectations.
• Skilled in QMS tools (e.g., FMEA, CAPA, 8D) and risk assessment.
• Certified Lead Auditor (ISO, BRC, FSC) and familiar with SEDEX 4-Pillar audits (preferably)
• Strong communication and cross-functional collaboration skills.
• Willing to travel up to 60% of the time across Europe and Asia.

Why Join Us?

• Be part of a growing global packaging leader .
• Take ownership of the regional quality strategy .
• Collaborate with diverse and dynamic teams .
• Access to career growth and competitive compensation .

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with GMP guidelines and regulatory requirements (e.g., FDA, EMA).
• Oversee all aspects of quality assurance, including batch record review, deviation management, CAPA, change control, and internal/external audits.
• Lead and mentor the QA team, fostering a culture of quality and compliance.
• Ensure that all pharmaceutical products manufactured meet stringent quality standards and regulatory specifications.
• Conduct regular risk assessments and implement mitigation strategies for quality-related issues.
• Review and approve validation protocols and reports for manufacturing processes and equipment.
• Liaise with regulatory agencies during inspections and provide necessary documentation.
• Manage vendor qualification programs and ensure supplier compliance.
• Drive continuous improvement initiatives within the QA department and manufacturing operations.
• Stay current with evolving GMP regulations and industry best practices.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 8 years of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
• Extensive knowledge of GMP regulations, ICH guidelines, and other relevant international standards.
• Proven experience in managing and leading QA teams.
• Demonstrated success in implementing and maintaining robust QMS.
• Strong understanding of pharmaceutical manufacturing processes, validation, and quality control.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional communication, interpersonal, and leadership abilities.
• Experience with regulatory inspections and audits is essential.
• Proficiency in quality management software and tools.

• Lead and manage the Pharmaceutical Quality Assurance department.
• Develop, implement, and maintain the company's Quality Management System (QMS).
• Ensure compliance with GMP, GDP, and other relevant pharmaceutical regulations.
• Conduct and manage internal and external audits (supplier and regulatory).
• Oversee the investigation of deviations, out-of-specifications, and customer complaints.
• Manage the CAPA (Corrective and Preventive Actions) system.
• Review and approve batch records, validation protocols, and reports.
• Provide QA support for product development, manufacturing, and release.
• Train and mentor QA personnel and other staff on quality principles and procedures.
• Act as a key point of contact during regulatory inspections.
• Drive continuous improvement initiatives within the QA function and across the organisation.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 8 years of experience in Pharmaceutical Quality Assurance.
• In-depth knowledge of GMP regulations and guidelines.
• Proven experience in managing Quality Management Systems, audits, deviations, and CAPAs.
• Strong understanding of pharmaceutical manufacturing processes and product lifecycle.
• Excellent leadership, team management, and interpersonal skills.
• Exceptional analytical, problem-solving, and decision-making abilities.
• Proficiency in quality risk management principles.
• Strong communication and presentation skills.
• Experience interacting with regulatory authorities (e.g., MHRA, FDA) is essential.