10 Manufacturing Companies jobs in Oldham

Title: QC Assistant
Location: West Yorkshire
Salary: 28,000-30,000
Term: Permanent

SRG is working with an independent contract manufacturer of personal care / skincare products, based in West Yorkshire. They are now looking for a quality control assistant to join the team. You would be responsible for wet chemistry / bench chemistry testing and techniques. Ensure products meet specifications, as well as some small-scale formulation projects. This position would be an excellent opportunity for someone with experience in Quality Control or lab-based testing to join a supportive, friendly, family-owned company.

Working Hours: Monday to Friday 7:30am to 4:15pm (Mon-Fri), 45-minute lunch break

Role / Description

• QC testing of raw materials, in-process samples and finished product to check batches meet specifications
• Development and implementation of SOP's and QC procedures
• Lab techniques include PH testing, viscosity, stability testing and packaging compatibility testing
• Conduct routine microbiological and physical testing on products to ensure batches are compliant against industry regulations
• Work in harmony with Production and QA to achieve production delivery plans and resolve any quality issues
• Collaborate with stakeholders to ensure R&D, production and packaging compliance and resolve any inconsistencies to ensure batch consistency
• Formulation and development of batches to help improve new and existing batches

Requirements

• 2+ years recent experience in QC testing / wet chemistry within the personal care / skincare industry
• Willing and able to work stood up in a Fast-paced manufacturing environment
• Experience of working to cosmetic regulations such as EU Cosmetics Regulation, UK REACH, FDA etc.
• Strong communication skills and can relay information accurately
• Full right to work in the UK - there is no sponsorship available for this role

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV For more information regarding this position or any others, please call Rhi on (phone number removed).

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

Keywords: formulation, NPD, new product development, new product innovation, packaging development, sustainable packaging, packaging trends, packaging innovation, supplier management, green chemistry, beauty, cosmetics, skincare, personal care, haircare, packaging innovation, soap, quality, quality control, quality assurance, sop's, haccap, ISO22716, Six Sigma, EU Cosmetics Regulation, UK REACH, FDA, manufacturing, ingredient safety

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Quality Control Engineer

Manchester and NW

Permanent

Competitive Salary + Car/Car Allowance + Flexible Benefits

Summary

We have an exciting new position available for a mechanically biased quality control engineer to join us at NG Bailey. The quality engineer will be responsible for supporting mechanical projects within the Northwest region, and must have experience of the installation of mechanical systems (wet and dry).

The quality control engineer will conduct all aspects of quality control and project compliance with the project specific QCMS, ensuring that the MEP systems meet the required regulator, legislative and specification standards before they reach the customer.  You will also provide guidance to the project quality team and relevant stakeholders, in all aspects of the project life cycle.  We will also be open to considering quality manager level.

Some of the key deliverables in this role will include:

• Demonstration appropriate health and safety awareness to ensure that the safety first and foremost message is visible and alive throughout all activities relating to the project.
• Work with the operations and commissioning teams to produce the project specific QCMS (quality control management system). Review and comment on work in progress drawings, to ensure accurate and relevant information is incorporated and drawings produced in accordance with relevant standards.
• Ensure all MEP systems to be installed are covered by an inspection and test plan, and that production, approval and completion is tracked.
• Monitor progress of installations and carry out surveillance of systems to ensure installation is in accordance with specification and standards.
• Work closely with the design and operation teams to ensure that NG Bailey preferred suppliers are used and engaged as early as possible.
• Work with supply chain manager to review quality of our supply chain, ensuring sub contractors understand and follow NGB internal procedures. Coordinate with sub contractors when information is required from them for any documentation.
• Ensure NGB approved products and materials are used, undertaking factory witness testing of major items of plan and equipment.
• Ensure relevant teams hold the necessary qualifications and competencies for which they are employed. Ensure any on site training requirements are taken. Carry out toolbox talks and deliver presentations where required.
• Undertake regular audits highlighting and escalating any non conformances or defects.  Identify and escalate any project risks.
• Provide project reviews and reports where appropriate.
• Coordinate with operations and commissioning team to produce project QC and commissioning action plan.

What we’re looking for:

Significant experience as an expert mechanical/HVAC engineer, or leader/supervisor with relevant mechanical qualifications:

• A good understanding of ventilation systems.
• Piped medical gas.
• Air Conditioning systems.
• Gas Safe and water regulations qualification. 
• Training will be available along with support from the wider QC function.
• A good understanding of modern and traditional installation methods (compliant to relevant standards).

CSCS Card, IOSH, CDM, SMSTS

Benefits:

We're always evolving our benefits to ensure we're attracting and retaining great people.  Some of what you can expect includes: 

• Car/Car allowance
• Salary sacrifice car scheme (Hybrid/Electric Vehicle)
• Pension with a leading provider and up to 8% employer contribution
• 25 days holiday
• Personal Wellbeing and Volunteer Days
• Private Medical Insurance
• Free 24/7 365 Employee Assistance Program to support mental health and well-being (including counselling sessions and legal advice)
• Flexible benefits to suit from Dental Insurance, Gym Memberships, Give As You Earn, Travel Insurance, Tax Free Bikes.
• Personal development programme

Next Steps: 

As a business, we’re on a journey to build on our culture where everyone is included, treated fairly and with respect. This starts with recruitment and how we bring people into the organisation.  

We’ll do our best to outline the recruitment process to you ahead of time with plenty of notice. If you require any accommodations to participate in the application or interview process, please let us know and we will work with you to ensure your needs are met. 

About Us: 

We are one of the leading independent engineering and services businesses in the UK. Founded in 1921, with a turnover of £500m and 3000 employees, we are proud of our history of developing great people through our investment in training. 

Working across a variety of sectors within the building and infrastructure industry, our innovative, responsible and forward-thinking approach allows us to work on fantastic ground-breaking projects, providing solutions using the latest tools and technologies. 

Progression is something we value, and we will make sure that when you join us you have a clearly defined development path, supported by regular reviews, training and ongoing support to enable you to be the best you can be. 

#LI-LO1

#LI-hybrid

Job Title: Quality Controller
Location: Blackburn with Darwen
Working Pattern: Full Time, 2pm to 10pm

Salary: Competitive + 10 Shift Allowance

Are you passionate about quality assurance and looking to make a difference in a dynamic environment?

We are currently seeking a dedicated and detail-oriented Quality Controller to join our team in Blackburn with Darwen. This is an exciting opportunity for someone who thrives in a fast-paced setting and is committed to maintaining high standards of quality throughout the production process.

Key Responsibilities:

Conduct regular inspections and assessments of products and processes to ensure compliance with quality standards.
Identify and report any quality issues or non-conformities, working closely with production teams to implement corrective actions.
Maintain accurate records of inspections, tests, and quality assurance activities.
Collaborate with team members to develop and improve quality control procedures and practises.
Assist in training staff on quality control measures and best practises to promote a culture of quality within the organisation.
Ensure that all safety and compliance regulations are adhered to in all aspects of the role.

What We're Looking For:

Previous experience in quality control or a related field is preferred.
Strong attention to detail and excellent analytical skills.
Effective communication skills, both verbal and written.
Ability to work independently as well as part of a team.
Familiarity with quality assurance methodologies and tools is a plus.
A valid driving licence is essential as travel may be required.

Benefits:

Competitive salary with a 10 shift allowance.
Opportunities for professional development and career advancement.
A supportive and collaborative work environment.
Employee discounts and benefits.

If you are ready to take your career to the next level and play a crucial role in maintaining our high-quality standards, we want to hear from you!

How to Apply:
Please submit your CV and a cover letter outlining your relevant experience and why you would be a great fit for this position.

Join us in ensuring excellence in our products and services. We look forward to welcoming a new Quality Controller to our dedicated team!

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

• Performing analytical tests on pharmaceutical samples.
• Operating and maintaining laboratory instrumentation.
• Analyzing test results and ensuring compliance with specifications.
• Documenting all laboratory activities according to GMP.
• Assisting with method development and validation.
• Participating in internal and external audits.
• Adhering to all safety protocols in the laboratory.
• Troubleshooting analytical issues.

• Performing complex analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
• Developing, validating, and transferring analytical methods.
• Interpreting test results, troubleshooting deviations, and investigating out-of-specification (OOS) results.
• Documenting all laboratory activities meticulously in compliance with Good Laboratory Practices (GLP) and regulatory guidelines (e.g., GMP).
• Preparing and reviewing analytical reports, Certificates of Analysis (CoAs), and method validation protocols.
• Maintaining laboratory equipment, ensuring calibration and proper functioning.
• Contributing to internal audits and regulatory inspections.
• Providing training and mentorship to junior analysts.
• Collaborating with R&D, production, and regulatory affairs teams to resolve quality issues.
• Staying updated on current industry trends, regulations, and scientific advancements.

• Performing analytical testing on raw materials, in-process samples, and finished pharmaceutical products.
• Utilising various analytical techniques and instrumentation, such as HPLC, GC, spectroscopy, and wet chemistry.
• Interpreting test results, documenting findings, and preparing analytical reports.
• Ensuring all laboratory activities comply with GMP, FDA, and other relevant regulatory standards.
• Maintaining laboratory equipment and ensuring its calibration and functionality.
• Investigating out-of-specification (OOS) results and identifying root causes.
• Collaborating with other departments, including R&D and manufacturing, to resolve quality issues.
  This is a critical role within the pharmaceutical industry, demanding precision and a deep understanding of scientific principles. As a remote-focused position, it offers flexibility while requiring strict adherence to procedures and deadlines. We are looking for an analytical thinker with excellent problem-solving skills and a commitment to maintaining the highest standards of quality. If you are a motivated scientist with experience in pharmaceutical quality control and are seeking a remote opportunity that offers significant impact, we encourage you to apply. Your expertise will be highly valued.
  Qualifications:
  
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
  • Proven experience as a Quality Control Analyst in the pharmaceutical industry.
  • Strong knowledge of analytical techniques (e.g., HPLC, GC, UV-Vis, IR spectroscopy).
  • Familiarity with GMP, ICH guidelines, and regulatory requirements.
  • Excellent laboratory data analysis and interpretation skills.
  • Proficiency in using laboratory information management systems (LIMS) and standard software.
  • Strong written and verbal communication skills.
  • Ability to work independently and manage workload effectively in a remote setting.
    

• Develop and implement quality control plans and procedures.
• Monitor manufacturing processes to ensure compliance with quality standards.
• Analyze production data, identify defects, and determine root causes.
• Implement corrective and preventive actions (CAPA).
• Conduct internal quality audits and assessments.
• Manage supplier quality and incoming material inspections.
• Utilize statistical process control (SPC) techniques.
• Prepare quality reports and document findings.
• Collaborate with production and engineering teams on quality initiatives.
• Ensure adherence to relevant quality management systems (e.g., ISO 9001).

• Bachelor's degree in Engineering (Mechanical, Manufacturing, or related) or equivalent experience.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
• Strong knowledge of quality management systems (ISO 9001) and methodologies (SPC, Six Sigma, Lean).
• Proficiency in data analysis and interpretation.
• Excellent problem-solving and analytical skills.
• Strong written and verbal communication skills.
• Ability to work independently and manage time effectively in a remote setting.
• Experience with quality control tools and software.