16 Manufacturing Companies jobs in Ashburton

Are you looking to join a successful technical company with a close-knit team, specialising in precision manufacturing and laser-based solutions? They pride themselves on quality, innovation, and teamwork.

We're looking for a reliable and detail-focused operative to join our Quality Control and Packing team. You'll be working with laser machinery to finish products, inspecting them for quality, and packing them to specification. Attention to detail is crucial to the role.

• Operate laser machines for product marking or finishing.
• Perform quality checks on finished items.
• Record inspection results and report any defects.
• Pack products securely and accurately.
• Maintain a clean and organised workspace.
• Work collaboratively to meet production goals.
• Follow health and safety procedures.

• Experience in a manufacturing or technical environment preferred but not essential.
• Comfortable working with machinery (training provided).
• Strong attention to detail.
• Good communication and teamwork skills.
• Reliable and punctual.

• Paid lunch break.
• Supportive team environment.
• On-the-job training.
• Flexible part-time schedule.
• Opportunity to grow within a technical field.

Apply today!

Acorn by Synergie acts as an employment business for the supply of temporary workers.

• Develop and refine quality control protocols and standards for production lines.
• Conduct comprehensive quality audits and inspections of raw materials, in-process components, and finished goods.
• Analyze quality data using statistical methods to identify trends, root causes of defects, and areas for improvement.
• Collaborate closely with design, engineering, and production teams to integrate quality considerations into product development cycles.
• Implement corrective and preventive actions (CAPA) and monitor their effectiveness.
• Train and mentor junior quality control personnel.
• Maintain detailed records of quality control activities, findings, and resolutions.
• Stay abreast of industry best practices, regulatory requirements, and emerging quality control technologies.
• Contribute to continuous improvement initiatives across the manufacturing process.

• Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
• Proven experience in a quality control or quality assurance role within a manufacturing environment.
• In-depth knowledge of quality management systems (e.g., ISO 9001) and statistical process control (SPC).
• Experience with quality inspection tools and methodologies.
• Strong analytical and problem-solving skills, with a meticulous attention to detail.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively across departments.
• Proficiency in data analysis software (e.g., Minitab, Excel).
• Experience in a remote working environment is a plus.

• Conducting analytical testing of pharmaceutical materials using various laboratory techniques, including HPLC, GC, UV-Vis spectroscopy, and dissolution testing.
• Interpreting analytical data, identifying deviations, and investigating out-of-specification (OOS) results.
• Documenting all laboratory activities accurately and contemporaneously in accordance with GMP guidelines.
• Preparing Certificates of Analysis (CoAs) and other quality-related documentation.
• Participating in method validation and transfer activities.
• Maintaining laboratory equipment and ensuring calibration schedules are met.
• Reviewing batch records and quality control data for completeness and compliance.
• Collaborating with cross-functional teams, including manufacturing, regulatory affairs, and R&D, to resolve quality issues.
• Staying up-to-date with relevant pharmacopoeias (e.g., USP, EP) and regulatory guidelines.
• Contributing to continuous improvement initiatives within the quality control function.
• Managing time effectively to meet project deadlines and analytical testing schedules.
• Communicating results and potential issues clearly and concisely to supervisors and team members via virtual platforms.

• Perform a wide range of analytical tests on pharmaceutical raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis Spectroscopy, and titration.
• Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
• Troubleshoot analytical instrumentation and testing issues, providing effective solutions.
• Analyze and interpret complex analytical data, generating accurate and comprehensive test reports.
• Ensure all laboratory activities comply with GMP, GLP (Good Laboratory Practice), and other relevant regulatory standards.
• Maintain laboratory equipment and ensure it is calibrated and qualified.
• Participate in internal and external audits, providing necessary documentation and explanations.
• Contribute to the continuous improvement of QC processes and laboratory operations.
• Mentor and train junior QC analysts, sharing expertise and best practices.
• Review and approve test data and documentation generated by other team members.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related scientific discipline.
• Minimum of 5 years of hands-on experience in pharmaceutical Quality Control.
• Proficiency in operating and maintaining analytical instruments, particularly HPLC and GC systems.
• Strong knowledge of pharmaceutical regulatory requirements (e.g., GMP, ICH).
• Experience with method development and validation.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong attention to detail and ability to maintain accurate records.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Proficiency in laboratory information management systems (LIMS) is a plus.

• Perform a variety of analytical tests on raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Interpret test data, evaluate results against specifications, and document findings accurately.
• Investigate Out-of-Specification (OOS) results and deviations, participating in root cause analysis.
• Maintain laboratory equipment, ensuring calibration and proper functioning.
• Adhere strictly to GMP, GLP, and other relevant regulatory requirements.
• Prepare and review analytical test reports, batch release documentation, and other quality records.
• Collaborate with R&D, manufacturing, and regulatory affairs departments.
• Contribute to the continuous improvement of QC processes and laboratory operations.
• Participate in internal and external audits and inspections.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
• Proficiency in a wide range of analytical techniques, including HPLC and GC.
• In-depth knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
• Experience with method validation and qualification.
• Strong understanding of data integrity principles.
• Excellent problem-solving, critical thinking, and documentation skills.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.

• Perform visual and mechanical inspections of incoming raw materials, in-process components, and finished goods.
• Utilize various measurement and testing equipment (e.g., calipers, micrometers, gauges, CMM) to verify product dimensions and specifications.
• Document inspection results accurately, identifying and reporting any non-conformances or defects.
• Follow established quality control procedures and checklists for different product lines.
• Collaborate with production and engineering teams to identify root causes of quality issues and recommend corrective actions.
• Assist in the development and implementation of new quality control processes and standards.
• Conduct audits of production processes to ensure compliance with quality management systems (e.g., ISO 9001, IATF 16949).
• Maintain accurate records of inspections, test results, and quality data.
• Ensure that all inspection equipment is calibrated and maintained properly.
• Participate in continuous improvement initiatives aimed at enhancing product quality and reducing waste.
• Adhere to all health and safety regulations within the manufacturing environment.

• Perform a wide range of analytical tests on raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, spectroscopy, wet chemistry).
• Develop, validate, and transfer analytical methods according to relevant guidelines (e.g., ICH, USP, EP).
• Analyze and interpret test results, ensuring accuracy and completeness.
• Document all laboratory activities, including test procedures, results, and deviations, in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Investigate out-of-specification (OOS) results and out-of-trend (OOT) data, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, ensuring it is calibrated, qualified, and in good working order.
• Contribute to the preparation of regulatory submission documents and respond to queries from health authorities.
• Train and mentor junior analysts, providing guidance on analytical techniques and laboratory procedures.
• Participate in internal and external audits, ensuring compliance with regulatory standards.
• Collaborate with other departments, including R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues.
• Stay updated on current industry trends, scientific advancements, and regulatory changes affecting pharmaceutical quality control.
• Ensure the safe handling and disposal of chemicals and laboratory waste.

• A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• A minimum of 5 years of hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Strong understanding of GMP, GLP, and relevant regulatory guidelines (e.g., ICH, FDA, EMA).
• Experience with method development and validation is essential.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong documentation and report-writing abilities.
• Good communication and interpersonal skills, with the ability to work effectively in a team.
• Experience with laboratory information management systems (LIMS) is a plus.
• The ability to work independently and as part of a collaborative team in a laboratory setting.

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR, titration).
• Develop, validate, and implement new analytical methods according to regulatory guidelines (e.g., ICH, GMP).
• Troubleshoot and maintain analytical instrumentation, ensuring accuracy and reliability of results.
• Interpret test results, prepare comprehensive analytical reports, and document all activities in compliance with Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results and deviations, recommending corrective and preventive actions (CAPAs).
• Collaborate with R&D, production, and regulatory affairs teams to support product development and lifecycle management.
• Mentor and train junior analysts, providing technical guidance and support.
• Participate in internal and external audits, ensuring compliance with quality standards.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Manage and maintain laboratory consumables and reagents inventory.

• BSc or MSc in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
• Proficiency in operating and maintaining analytical instruments such as HPLC, GC, and spectrophotometers.
• Strong knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceutical testing.
• Excellent analytical, problem-solving, and documentation skills.
• Ability to work independently and as part of a team in a fast-paced environment.
• Experience with method validation and transfer is essential.
• Good communication skills, both written and verbal.