What Jobs are available for Manufacturing Companies in East Kilbride?
Showing 7 Manufacturing Companies jobs in East Kilbride
Quality Control Inspector
Posted 27 days ago
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Job Description
**Location:** Renfrew, Scotland, United Kingdom, PA4 8XJ
**Company:** Chart Industries
**The Role**
The main purpose of the Quality Control Inspector role is as follows:
+ To carry out inspection of components, assemblies and documentation to ensure compliance to product and package standards
+ Implementation and maintenance of the Business Management System (BMS) according to ISO9001 standard
+ Support Value Stream delivery teams where required in meeting customer delivery commitments
This is a permanent role based from our HQ in Renfrew, paying £37,500. The shift pattern is straight dayshift, with working hours being either 07.00 - 15.15 (Mon- Thurs) and 07.00 - 13.00 (Friday) OR 08.00 - 16.15 (Mon - Thurs) and 08.00 - 14.00 (Friday).
**Who are we?**
Howden has a range of compressors, blowers, fans, steam turbines, and rotary heat exchangers, and has been at the forefront of developing engineered solutions for the needs of industrial processes since 1854. In 2023, Howden joined forces with Chart Industries, a global leader in engineered equipment for clean energy and industrial gas markets.
Together, we operate over 64 manufacturing sites and 50+ service centres worldwide, with 11,700+ employees driving innovation in hydrogen, carbon capture, energy recovery, nuclear, water treatment, mining, and LNG. As part of the Nexus of Clean, we are advancing a sustainable future-helping customers improve efficiency and reduce emissions across clean power, water, food, and industrial sectors.
Join us and be part of a purpose-driven team shaping the future and tackling some of the planet's most urgent challenges, all while growing your career in a dynamic global environment.
**What will you do?**
+ Inspection of components, assemblies and documentation at goods receipt, in process, suppliers and prior to final despatch to ensure compliance with required specifications.
+ The initiation, monitoring and close out of corrective actions where deficiencies in materials, manufacture and design are found
+ Create and maintain inspection records to accurately reflect end to end product manufacturing and packaging activities
+ Ensure correct calibration of measuring equipment used in manufacture and inspection. Appraisal of new measuring equipment and / or techniques to ensure cost effectiveness
+ Work alongside Documentation Control team to ensure all project related documentation is accurate, on time and meets customer expectation levels
+ Review & approve relevant supplier documentation such as weld procedures, NDE procedures, Hydrotest procedures and material certification etc in accordance with code & client requirements
+ Liaise with clients & witnessing authorities to meet contract requirements. Support inspection/process review activities at Sub-Contractors Works
+ Comply with relevant work standard instructions in line with HCO Business Management System (BMS)
+ Use CBS approach to promote Built in Quality concepts into Standard work. Collaborate with Operations, Engineering, Commercial and Procurement teams to drive improved manufacturing and supply chain performance and early defect detection
+ Ensure adherence to company environmental, health and safety standards in compliance with company policies to ensure a safe working environment and the minimisation of environmental impact.
**What do you bring?**
An ideal candidate would likely have the following profile:
+ ONC/HNC in an engineering subject and / or proven relevant experience in Quality
+ Problem solving ability, capable of thinking laterally and coming up with innovative solutions
+ Experience of using a wide range of standard inspection and test equipment
+ Competence in understanding of engineering drawings and specifications
+ Experience of the control and maintenance of quality reports and records
+ Experience of planning, completing, reporting and follow up of inspection activities
+ Good communication skills
+ Application of one or more ERP systems to a good working level
**We've put together some criteria that we think is important for this role, but don't worry if your experience and expertise isn't an exact match. If you feel that you can add value to our role and to Howden more broadly, we would welcome your application and be eager to learn more about you.**
**Our Benefits**
This is a permanent role based from our HQ in Renfrew, paying £37,500. The shift pattern is straight dayshift, with working hours being either 07.00 - 15.15 (Mon- Thurs) and 07.00 - 13.00 (Friday) OR 08.00 - 16.15 (Mon - Thurs) and 08.00 - 14.00 (Friday).
Our benefits includes:
+ Generous holiday entitlement package totalling 33 days annual leave
+ Howden Pension Plan with a maximum employer contribution of 7%
+ Enhanced Maternity, Paternity, shared parental and adoption leave pay
+ Company electric vehicle scheme
+ Free onsite parking
+ Healthcare cash plan
+ Group Life Assurance plan at 3x salary
+ Group Income Protection plan
+ Access to My Howden Benefits & Wellbeing Portal - Cycle2Work programme, range of discounts across various retailers, wealth of information to support health & wellbeing
+ Dedicated Service - free counselling, physiotherapy, financial support, medical second opinion, remote GP, personal training, nutrition consultations etc
+ Opportunity to be involved in our ESG 'Bright Future' initiatives - STEM ambassador & volunteering
Chart Industries is an equal employment opportunity (EEO) employer and will not discriminate against any employee or applicants because of his or her race, color, religion, sex, gender identity or expression, sexual orientation, pregnancy, age, national origin, disability, veteran status, military status, marital status, genetic information or any other reason prohibited by law. Additionally, it is and shall continue to be our policy to provide promotion and advancement opportunities in a non-discriminatory fashion.
Chart complies with applicable local, state, and federal statutes governing "equal employment opportunity" and nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including hiring, placement, promotion, termination, layoff, recall, transfers, leave of absence, compensation and training.
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                    Manager Quality Control, Dalry
Posted today
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Job Description
**Location:** Dalry, UK
We have one permanent vacancy within the Quality Department working on dayshift.
At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated.
**Key responsibilities:**
+ Manage QC activities of the twenty-five personnel in the Laboratory team, across five on-site laboratories, in support of a high-volume production plant, working to pharma Good Manufacturing Practice (GMP) standards
+ Provide an efficient QC service within site budget requirements
+ Ensure that all laboratory work is correctly conducted to meet GMP requirements as well as ISO 9001, regulatory and company quality management standards
+ Ensure routine maintenance and calibration of equipment, and the control and maintenance of all laboratory consumables, raw materials, standard solutions and retained samples
+ Ensure the transfer, trial and validation of all newly developed analytical methods are successful, in collaboration with company and regulatory requirements
+ Provide technical expertise on new analytical methods and where applicable provide advice and support when troubleshooting any complex methodologies or technical equipment
+ Write/review Quality and Safety documentation including SOP's, risk assessments and stability reports as applicable
+ Support and adhere to company HS&E policies and procedures
+ Management of the leadership team, assigning objectives and priorities to deliver outstanding service
+ Drive continuous improvement within the QC environment, including but not limited to, Laboratory Automation, upgrades to equipment and laboratory facilities, method and process improvement and new technology horizon scanning and implementation.
+ Local Management and support of the laboratory systems e.g. Chromatography Data System, LIMS system
+ Co-ordinating, leading and responding to customer, regulatory, and third-party quality audits
+ Collaboration with dsm-firmenich colleagues, including those off-site, to support information requests for customers, technical support and regulatory requirements
+ Support investigation of customer complaints, deviations and technical issues on plant
+ Providing advice and support to dsm-firmenich employees and management as required
+ Conducting internal quality audits to review site practices against relevant Quality and GMP standards food, feed, cosmetic and pharma standards
+ Team development, including maintaining competence and undertaking on-going continuous personal development of themselves and the team to ensure maintenance of current knowledge and best practice
+ Optimally deploy people to ensure succession planning and employee development, ensuring the short-term and long-term availability of a competent workforce to meet the current and future requirements of the organization
+ Other activities to improve quality and compliance as assigned by the Quality Manager
**We offer:**
+ A workplace with a strong focus on the work environment and a positive atmosphere.
+ A motivating and professional work setting within a highly skilled and successful team.
+ A position offering the opportunity to develop your skills and quickly expand your area of responsibility, based on demonstrated performance.
+ Many opportunities for learning and development, both in technical and personal areas.
+ A full-time position with a salary aligned with your qualifications.
**You Bring:**
+ Successful candidates will be expected to have a degree or equivalent in Chemistry or related scientific discipline with a minimum of seven years relevant industrial experience, three of which in a relevant people management role, preferably within a GMP lab environment.
+ A thorough knowledge of pharmaceutical GMP is considered essential along with a comprehensive understanding of analytical chemistry as well as organic/inorganic chemistry.
+ Experience of HPLC, GC and Titration including trouble shooting is essential, experience of AAS and ICP desirable.
+ Strong understanding of Laboratory safety requirements and a commitment to a robust safety culture is a requirement.
+ Other necessary behaviors are ownership of issues, strong communication and facilitation skills as well as appropriate due diligence and attention to details
**About dsm-firmenich**
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we **go beyond, together.**
**Our application process**
Interested in this position? Please apply on-line by uploading your resume in English via our career portal ( belonging and equal opportunity statement**
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to
**Agency Statement**
Please note this is a direct search led by dsm-firmenich. We only accept applications from candidates, not from agencies nor subject to agency's fees, percentages or similar.
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                    Senior Quality Control Inspector
Posted 7 days ago
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Job Description
Key Responsibilities:
- Develop and implement quality control inspection plans and procedures.
- Conduct visual and dimensional inspections of raw materials, components, and finished products.
- Utilize precision measuring instruments and testing equipment for quality assessment.
- Identify, document, and report product defects and non-conformities.
- Analyze root causes of quality issues and recommend corrective actions.
- Ensure adherence to quality standards, specifications, and regulatory requirements.
- Collaborate with production and engineering teams to resolve quality concerns.
- Maintain accurate inspection records and prepare quality reports.
- Train and mentor junior quality control inspectors.
- Contribute to the continuous improvement of quality management systems.
- Proven experience as a Quality Control Inspector in a manufacturing environment, with at least 5 years in a senior capacity.
- Strong understanding of manufacturing processes and quality control methodologies.
- Proficiency in using precision measuring instruments (e.g., calipers, micrometers) and testing equipment.
- Ability to read and interpret technical drawings, blueprints, and specifications.
- Excellent analytical, problem-solving, and attention-to-detail skills.
- Experience with quality management systems (e.g., ISO 9001) is highly desirable.
- Ability to work independently and manage workload effectively in a remote setting.
- Strong communication and documentation skills.
- Relevant certifications in quality control are an advantage.
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                    Senior Quality Control Chemist
Posted 10 days ago
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Job Description
The Senior Quality Control Chemist will lead the development, validation, and implementation of analytical methods for raw materials, in-process samples, and finished products. You will conduct advanced chemical analyses, interpret results, and generate comprehensive reports. This role involves troubleshooting quality issues, collaborating with R&D and production teams to resolve manufacturing challenges, and ensuring that all quality control activities comply with regulatory requirements and internal standards. You will also play a key role in mentoring junior chemists and contributing to the continuous improvement of our quality management systems.
We are seeking candidates with a Bachelor's or Master's degree in Chemistry, Analytical Chemistry, or a closely related field, coupled with a minimum of 5 years of hands-on experience in quality control laboratories, preferably within the chemical or pharmaceutical industry. A deep understanding of analytical techniques (e.g., HPLC, GC, Spectroscopy, Titration) and GMP/GLP principles is essential. Proven experience in method development, validation, and laboratory instrumentation is required. Excellent analytical, problem-solving, and organisational skills, along with strong written and verbal communication abilities, are paramount. Experience in a remote laboratory setting or managing quality remotely is a distinct advantage.
This is an exceptional opportunity to apply your advanced chemical knowledge and quality assurance expertise in a leading company that values scientific rigour and innovation. Working remotely, you will have the autonomy to drive quality standards and contribute to the development of cutting-edge chemical products. You will be part of a collaborative environment that encourages professional development and rewards excellence. Your dedication to quality will be instrumental in our ongoing success.
Responsibilities:
- 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.
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                    Senior Quality Control Inspector - Manufacturing
Posted 23 days ago
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Job Description
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                    Remote Pharmaceutical Quality Control Analyst
Posted 26 days ago
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Job Description
- 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.
A Bachelor's or Master's degree in a relevant scientific discipline (e.g., Chemistry, Pharmacy, Biochemistry) is required. Significant experience in pharmaceutical quality control or quality assurance is essential. Proficiency in data analysis software and a strong understanding of statistical process control are highly desirable. Excellent written and verbal communication skills are crucial for effective remote collaboration and reporting. If you are a seasoned Quality Control professional passionate about ensuring drug safety and efficacy and seeking a flexible remote work arrangement, we encourage you to apply.
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                    Senior Quality Control Inspector (Automotive Manufacturing)
Posted 18 days ago
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Job Description
Key Responsibilities:
- 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.
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