Technical Operations

Technical Operations

DSJ Global: Your Leading Partner for Technical Operations Talent

DSJ Global is a leading talent partner delivering mid-senior end-to-end supply chain talent. We secure business-critical Technical Operations talent through permanent, contract, and multi-hire recruitment solutions.

With 15 years of experience in overcoming extensive hiring challenges, DSJ Global is well-positioned to provide tactical solutions to your talent shortages across the entiresupply chain, enabling you to hire the right talent to help you achieve optimal supply and demand goals.

If youโ€™re looking to secure top talent within the Technical Operations sector or youโ€™re a professional searching for your next Technical Operations opportunity, our specialized team at DSJ Global nurtures candidates and clients to align personal and business opportunities.

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Benefits of Working with DSJ Globalโ€™s Technical Operations Team

DSJ Global's specialist Technical Operations team is dedicated to optimizing operational efficiency through innovation and advanced technology. The industry's increasing demand for streamlined processes, automation, and sustainable practices has fueled remarkable growth for Technical Operations professionals, amplified by the enduring impact of global events.

For immediate Technical Operations placements or strategic talent sourcing, DSJ Global's experienced team offers a wealth of expertise and comprehensive resources, ensuring exceptional outcomes. Partnering with DSJ Global's Technical Operations team brings distinct advantages:

15 years of experience and professional knowledge in the supply chain Technical Operations industryโ€‹

Access to an exclusive global network of both active and passive Technical Operations candidates

Guidance and advice from our global award-winning talent experts in the supply chain Technical Operations industry

โ€‹Embark on your talent journey by engaging with our expert team. Complete our form, and let us share how DSJ Global can collaborate effectively with your organization to fulfill your recruitment requirements.

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Technical Operations Jobs

Operations Superintendent

Job Description: The Operations Superintendent is responsible for overseeing the daily operations of the refinery. This includes managing operations personnel, ensuring safety and environmental compliance, meeting production targets, and maintaining product quality. The role requires advanced technical knowledge, leadership, and management skills to guide operations, resolve issues, and mentor personnel. The superintendent is also tasked with collaborating across departments to improve operational efficiency and safety. Responsibilities: Lead and develop operations personnel, ensuring skills development and accountability. Direct Operations Supervisors to achieve production and specification targets. Drive safety and environmental culture, ensuring compliance and positive outcomes. Provide guidance to inspection, project engineering, and other refinery departments. Supervise and develop Supervisors, building accountability and performance. Manage specific projects and participate in cross-functional initiatives. Requirements: High school diploma required; BS in Chemical Engineering preferred. 10+ years of progressive refinery experience and operations leadership. Knowledge of refinery processes and technology. Strong problem-solving, troubleshooting, and prioritization skills.

US$150000 - US$210000 per annum
Oklahoma
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Sr. Quality Manager

**Sr. Quality Manager Opportunity in Charles City, IA - Biotechnology Sector** Are you a seasoned leader passionate about quality management and biotech? An esteemed organization located in the vibrant community of Charles City, Iowa is searching for a Sr. Quality Manager to spearhead their dynamic team within the biotechnological field. This permanent role not only demands an individual with substantial experience overseeing multiple laboratories but also one who brings expertise specifically from fermentation processes. You will be at the forefront of managing four pivotal labs that are central to our operations: Fermentation, Chemistry, Microbiology and Entomology. We expect: - A minimum of 5 years' leadership experience. - Proven track record working with ISO/IEC 17025 standard. - Deep knowledge and hands-on involvement in fermentation-based practices or settings. Critical skills include: *Quality Management*: Ensure excellence across all laboratory functions by implementing robust procedures compliant with industry standards such as ISO/IEC 17025. *Leadership*: Lead your teams effectively through mentorship and strategic oversight while fostering a culture committed to high-quality outcomes. *Fermentation Expertise*: Apply your specialized understanding of biological process involving microorganisms which is critical given its application throughout various stages of production within this sector. Join us if you're ready for an exciting challenge where your contributions significantly impact both operational efficiency & product integrity!

Negotiable
Libertyville
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Sr. Quality Manager

**Sr. Quality Manager Opportunity in Charles City, IA - Biotechnology Sector** Are you a seasoned leader passionate about quality management and biotech? An esteemed organization located in the vibrant community of Charles City, Iowa is searching for a Sr. Quality Manager to spearhead their dynamic team within the biotechnological field. This permanent role not only demands an individual with substantial experience overseeing multiple laboratories but also one who brings expertise specifically from fermentation processes. You will be at the forefront of managing four pivotal labs that are central to our operations: Fermentation, Chemistry, Microbiology and Entomology. We expect: - A minimum of 5 years' leadership experience. - Proven track record working with ISO/IEC 17025 standard. - Deep knowledge and hands-on involvement in fermentation-based practices or settings. Critical skills include: *Quality Management*: Ensure excellence across all laboratory functions by implementing robust procedures compliant with industry standards such as ISO/IEC 17025. *Leadership*: Lead your teams effectively through mentorship and strategic oversight while fostering a culture committed to high-quality outcomes. *Fermentation Expertise*: Apply your specialized understanding of biological process involving microorganisms which is critical given its application throughout various stages of production within this sector. Join us if you're ready for an exciting challenge where your contributions significantly impact both operational efficiency & product integrity!

Negotiable
Libertyville
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Quality Specialist

We are seeking a dedicated and detail-oriented Quality Specialist to join our team at a leading Appliances, Electrical, and Electronics Manufacturing company in Concord, CA. In this role, you will play a critical part in ensuring the highest quality standards are maintained throughout the manufacturing process for our products. You will collaborate with various departments to implement and uphold quality control measures, ensuring compliance with industry standards and customer requirements. Key Responsibilities: Conduct regular inspections and audits of manufacturing processes, components, and finished products to ensure compliance with internal and external quality standards. Develop, implement, and maintain quality control procedures, standards, and specifications for the production of appliances, electrical, and electronic products. Review and analyze data related to product defects, production processes, and customer feedback to identify areas for improvement. Work closely with the production and engineering teams to resolve quality issues and implement corrective actions. Assist in the development and execution of test protocols, inspections, and documentation to ensure quality assurance compliance. Monitor and maintain records of quality metrics, non-conformances, and corrective actions taken. Conduct root cause analysis of quality issues and implement continuous improvement initiatives to prevent recurrence. Ensure that products meet safety, regulatory, and industry-specific standards (e.g., UL, CE, ISO, etc.). Collaborate with suppliers to ensure the quality of incoming raw materials and components. Assist in training and educating team members on quality standards and best practices. Maintain up-to-date knowledge of industry trends, quality control techniques, and regulatory requirements. Qualifications: Bachelor's degree in Engineering, Manufacturing, Quality Assurance, or a related field (preferred). Minimum of 3 years of experience in quality control or quality assurance in an appliance, electrical, or electronics manufacturing environment. Strong knowledge of quality management systems, industry standards, and regulatory requirements (e.g., ISO 9001, UL, CE). Experience with inspection tools and techniques such as calipers, micrometers, and other measurement devices. Proficient in data analysis and problem-solving using software tools (e.g., Excel, Minitab, SAP). Strong communication and interpersonal skills with the ability to work cross-functionally with various teams. Detail-oriented with a keen eye for identifying and solving quality-related issues. Ability to thrive in a fast-paced, dynamic work environment and manage multiple priorities. Salary: $70k-80k + Bonus + Benefits If you are interested, don't hesitate to apply!

US$70000 - US$80000 per annum
Concord
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Americas Quality Assurance Director

Join a leading global medical device manufacturing company committed to advancing health care through innovative products and solutions. We are seeking a highly experienced and strategic Senior Director of Quality to oversee our global quality assurance and regulatory compliance initiatives. The ideal candidate will have extensive experience in quality management within the medical device industry, with a strong focus on multisite oversight responsibilities. The position is in Massachusetts and the company is offering relocation assistance. Key Responsibilities: Lead and manage the global quality assurance strategy, ensuring compliance with all regulatory standards, including FDA, ISO 13485, and other relevant international regulations. Oversee quality management systems across multiple manufacturing sites, ensuring consistency and alignment with corporate quality objectives. Develop and implement policies and procedures to ensure quality standards are met and continuously improved. Collaborate with cross-functional teams, including R&D, operations, and supply chain, to integrate quality into all aspects of product development and manufacturing. Drive the development and execution of quality improvement initiatives, including root cause analysis and corrective action processes. Establish and maintain effective communication with regulatory agencies and ensure timely reporting and resolution of any compliance issues. Provide leadership and mentorship to quality assurance teams across multiple sites, fostering a culture of quality and accountability. Monitor industry trends and emerging regulations to proactively address potential impacts on quality practices. Qualifications: Bachelor's degree in Engineering, Life Sciences, or a related field; advanced degree preferred. Minimum of 10 years of experience in quality management within the medical device industry, with at least 5 years in a leadership role. Proven experience in multisite oversight, managing quality operations across multiple manufacturing facilities. Strong knowledge of FDA, ISO, and other global regulatory requirements for medical devices. Exceptional analytical and problem-solving skills, with a track record of driving quality improvements. Excellent communication and interpersonal skills, with the ability to influence at all levels of the organisation. Demonstrated ability to lead and motivate teams in a fast-paced, global environment. Salary: $200k-225k + Bonus + Benefits If you are interested, don't hesitate to apply!

US$190000 - US$225000 per annum
Milford
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EHS&S Site Manager

Summary: This role will collaborate with Planning, Production, Maintenance, Quality Control, and Engineering, as well as other functions as needed. Required: Preferred- BS degree in EHS, Industrial Hygiene, Science, or Engineering A minimum of 3-5 years of EHS&S experience, with a strong preference for experience in a chemical manufacturing PSM environment. Demonstrated knowledge of regulations including, but not limited to, pertinent Local/State/Federal EPA, OSHA, PSM, DHS, and DOT regulations. Recommended: Advanced coursework in EHS, Industrial Hygiene, and chemical industry experience. Proven continuous improvement skills. ISO 9001, ISO 14001, and Responsible Care Management Systemยฎ (RCMSยฎ) experience preferred. Hazardous materials management certification, certified EHS & Quality Auditor, Certified Safety Professional, Certified Associate Safety Professional, and/or Certified Industrial Hygienist. Experienced in effective application of root cause and failure analysis tools. Principal Accountabilities and Measures: Safety-Sensitive: Must pass regular & routine chemical dependency testing, annual respirator qualitative fit testing, and annual medical monitoring as required for certain tasks. Continuous Improvement: Improvement in the site safety culture and employee safety measured by defined leading safety indicators. Safety Performance: Measured by work-related accidents, near-miss accidents, and safety violations. Corrective Actions/Preventive Actions (CAPAs): Successful and timely completion of all CAPAs. Safety and Environmental Performance: Measured by consistent compliance with all local/state/federal regulations.

US$115000 - US$135000 per year
Houston
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Senior Engineer, Operational Excellence

JOB SUMMARY This role offers an excellent opportunity for a motivated and skilled individual to join our client's global Operational Excellence (OPEX) team. Reporting to the plant OPEX Manager, the Senior Engineer will focus on fostering a culture of operational and customer excellence, driving continuous improvement (CI) initiatives, and implementing changes to enhance performance in quality, delivery, and cost while ensuring safety. JOB DESCRIPTION Our client is a leading global medical technology company dedicated to advancing health through innovative solutions. The company values creativity and teamwork, supporting its employees to grow and excel. Join us and become part of a team that makes transformative changes possible. RESPONSIBILITIES Participate actively in the Focused Improvement team. Enhance problem-solving skills at all levels. Support CI projects across various dimensions, including quality, safety, delivery, and cost (SQDC). Coordinate component and project teams to reduce losses and achieve strategic goals. Contribute to the development and execution of a multi-year Cost to Win (CtW) portfolio, including governance and optimization efforts. Teach and mentor in Excellence concepts, including strategy deployment and Zero Loss mentality. Lead Kaizen events and support other Excellence components in developing problem-solving skills. Promote a zero-loss mindset to improve safety, quality, and cost. Guide project selection to focus resources on high-priority areas. Align Key Performance Indicators (KPIs) with strategic goals and support BD Excellence deployment. Drive advanced methodologies and support long-term CI objectives through cross-functional teams. Utilize data-driven visual management techniques to enhance metrics such as OEE, waste, and productivity. Contribute to key plant decisions and resource planning. Represent the company externally as needed. Operate with a high degree of autonomy, managing own work direction and tasks. Make decisions that impact cost, productivity, CtW performance, and OPEX budget. Qualifications Bachelor's degree or equivalent experience in Engineering. Proven experience with Lean and Six Sigma methodologies; Green or Black Belt certification preferred. Strong commitment to safety, customer satisfaction, and operational excellence. At least 3 years of manufacturing experience in a plant environment. Understanding of how operational excellence impacts customer service. Excellent communication skills, both verbal and written, across all levels. Proven track record in project or program management. Experience in multi-site and multi-cultural settings. Ability to link projects to business results and develop compelling business cases for resource investment, adhering to finance policies.

Negotiable
South Carolina
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EHS&S Site Manager

Summary: This role will collaborate with Planning, Production, Maintenance, Quality Control, and Engineering, as well as other functions as needed. Required: Preferred- BS degree in EHS, Industrial Hygiene, Science, or Engineering A minimum of 3-5 years of EHS&S experience, with a strong preference for experience in a chemical manufacturing PSM environment. Demonstrated knowledge of regulations including, but not limited to, pertinent Local/State/Federal EPA, OSHA, PSM, DHS, and DOT regulations. Recommended: Advanced coursework in EHS, Industrial Hygiene, and chemical industry experience. Proven continuous improvement skills. ISO 9001, ISO 14001, and Responsible Care Management Systemยฎ (RCMSยฎ) experience preferred. Hazardous materials management certification, certified EHS & Quality Auditor, Certified Safety Professional, Certified Associate Safety Professional, and/or Certified Industrial Hygienist. Experienced in effective application of root cause and failure analysis tools. Principal Accountabilities and Measures: Safety-Sensitive: Must pass regular & routine chemical dependency testing, annual respirator qualitative fit testing, and annual medical monitoring as required for certain tasks. Continuous Improvement: Improvement in the site safety culture and employee safety measured by defined leading safety indicators. Safety Performance: Measured by work-related accidents, near-miss accidents, and safety violations. Corrective Actions/Preventive Actions (CAPAs): Successful and timely completion of all CAPAs. Safety and Environmental Performance: Measured by consistent compliance with all local/state/federal regulations.

US$110000 - US$125000 per year
Houston
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Utilities Manager

Position Overview: The Utilities Manager is responsible for overseeing the operation, maintenance, and optimization of all utility systems within a pharmaceutical manufacturing facility. This includes managing systems such as steam, water, HVAC, compressed air, and other essential services to ensure reliable, efficient, and compliant operations in support of manufacturing processes. Key Responsibilities: Manage the day-to-day operations of utility systems, ensuring they meet production and regulatory requirements. Lead a team of technicians in the maintenance, troubleshooting, and repair of utility systems. Develop and implement preventive maintenance schedules to minimize downtime. Monitor utility performance, track energy consumption, and identify opportunities for cost reduction and process optimization. Ensure compliance with all relevant regulatory standards (e.g., GMP, OSHA, EPA). Collaborate with engineering and production teams to support facility upgrades and continuous improvement projects. Maintain utility-related documentation and reporting, including regulatory filings and operational logs. Qualifications: Bachelor's degree in Engineering, Facilities Management, or related field. Minimum of 5 years of experience in utilities management within a pharmaceutical or similar regulated manufacturing environment. Strong knowledge of utility systems (HVAC, water treatment, steam, compressed air, etc.). Familiarity with GMP, FDA, and other regulatory compliance requirements. Excellent leadership, problem-solving, and communication skills.

US$130000 - US$150000 per annum
England
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Supplier Quality Engineer

Job Overview: This role is crucial in ensuring that all materials, components, and products supplied to our company meet the highest quality standards. The Senior Supplier Quality Engineer will collaborate closely with internal stakeholders and external suppliers to monitor and improve quality performance, resolve supplier-related quality issues, and contribute to the continuous improvement of our manufacturing processes. Key Responsibilities: Supplier Management and Auditing: Lead the selection, evaluation, and performance monitoring of suppliers to ensure compliance with industry standards and company specifications. Conduct supplier audits, assessments, and evaluations to identify risks and ensure the supply chain meets regulatory, environmental, and safety requirements. Manage supplier quality agreements, ensuring alignment with manufacturing and regulatory standards. Quality Assurance and Compliance: Develop and implement quality assurance processes and procedures for incoming materials and components. Ensure that all materials and chemicals supplied meet established quality criteria and regulatory standards. Work closely with suppliers to address non-conformance issues and ensure corrective actions are taken promptly. Review and approve supplier documentation, such as certificates of analysis (COA) and material specifications. Root Cause Analysis and Problem Solving: Investigate and resolve supplier quality issues by conducting thorough root cause analysis (RCA) and implementing corrective actions. Collaborate with internal teams (e.g., production, R&D, and procurement) to troubleshoot quality issues and ensure effective solutions. Lead efforts in continuous improvement initiatives within the supply chain and manufacturing processes. Process Improvement and Innovation: Drive initiatives for improving supplier performance, focusing on reducing defects, increasing efficiency, and enhancing product quality. Work with suppliers to optimize quality control processes, improve reliability, and maintain cost efficiency. Contribute to the development and implementation of new quality tools, technologies, and systems. Data Analysis and Reporting: Analyze supplier performance data and quality metrics, preparing reports for management review. Track key performance indicators (KPIs) related to supplier quality and provide recommendations for improvement. Assist in preparing documentation for regulatory submissions and audits. Cross-functional Collaboration: Collaborate with procurement, engineering, production, and R&D teams to ensure seamless integration of supplier materials into the manufacturing process. Provide technical guidance and training to internal teams on supplier quality processes and expectations. Qualifications: Education: Bachelor's degree in Chemical Engineering, Materials Science, Chemistry, or a related field. A Master's degree is a plus. Experience: Minimum of 5-7 years of experience in supplier quality engineering, preferably in the chemical manufacturing or related industries. Strong knowledge of quality management systems (QMS), ISO 9001, and other relevant industry standards. Experience with root cause analysis tools (e.g., 8D, Fishbone, FMEA) and corrective/preventive actions (CAPA).

US$130000 - US$140000 per annum
North Kingstown
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Production Supervisor

Job Description: The ideal candidate will ensure production goals are met while maintaining the highest standards of safety, quality, and efficiency. Key responsibilities include supervising production staff, managing workflow, monitoring equipment, ensuring compliance with safety regulations, and implementing continuous improvement initiatives. The Production Supervisor will work closely with cross-functional teams to optimize processes and meet production targets. Key Responsibilities: Supervise and lead production teams to meet daily manufacturing targets. Ensure adherence to safety protocols and regulatory compliance. Monitor equipment performance and troubleshoot issues to minimize downtime. Coordinate with maintenance, quality control, and other departments to maintain optimal production flow. Train, coach, and evaluate production staff to foster a high-performance environment. Implement continuous improvement strategies to increase efficiency and reduce costs. Qualifications: A degree in Engineering (Chemical, Mechanical, Industrial, or related field) is required. Previous experience in chemical manufacturing or a related field. Strong leadership and team management skills. Excellent problem-solving and organizational abilities. Familiarity with safety regulations and quality control standards.

US$90000 - US$115000 per annum
North Kingstown
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Maintenance Manager

Position Overview: We are seeking a highly skilled and dedicated Manufacturing Maintenance Manager to oversee and manage the maintenance operations in our manufacturing facility. This role is critical in ensuring the reliability, safety, and efficiency of all production equipment and machinery. The ideal candidate will have strong leadership abilities, a deep understanding of manufacturing processes, and the technical expertise to troubleshoot and resolve complex mechanical and electrical issues. Key Responsibilities: Maintenance Strategy Development: Develop and implement preventive and predictive maintenance programs to minimize equipment downtime and extend the lifespan of machinery. Analyze production data to identify areas for improvement in maintenance practices and machine reliability. Team Leadership: Lead, mentor, and manage a team of maintenance technicians and engineers, ensuring high levels of performance, safety, and productivity. Conduct regular training and development programs to enhance technical skills and safety awareness. Equipment Management: Oversee the installation, repair, and calibration of manufacturing equipment and machinery. Troubleshoot mechanical, electrical, and electronic issues to ensure minimal disruption to production. Maintain and update equipment manuals, schematics, and maintenance records. Safety and Compliance: Ensure all maintenance activities are performed in compliance with safety regulations and company policies. Conduct regular safety audits and risk assessments to identify potential hazards. Ensure all tools, equipment, and machinery meet regulatory standards and are safe for use. Budget and Resource Management: Manage the maintenance budget, ensuring cost-effective purchasing of parts, tools, and supplies. Work with procurement and supply chain teams to ensure timely availability of spare parts and materials. Track maintenance expenses and report on cost-saving initiatives. Continuous Improvement: Lead initiatives to improve maintenance processes, reduce downtime, and increase operational efficiency. Collaborate with production teams to schedule maintenance work during downtime to minimize impact on production goals. Collaboration with Other Departments: Work closely with production, engineering, and quality control teams to understand maintenance needs and troubleshoot issues. Participate in cross-functional meetings to provide input on equipment upgrades, new technologies, and process improvements. Qualifications: 7+ years of experience in Manufacturing Maintenance Management In-depth knowledge of mechanical, electrical, hydraulic, and pneumatic systems used in manufacturing. Strong leadership and team management skills, with a track record of building and maintaining high-performing teams. Proficiency with computerized maintenance management systems (CMMS) and other maintenance-related software. Excellent problem-solving, communication, and organizational skills. Ability to work in a fast-paced, high-pressure environment and manage multiple priorities.

US$100000 - US$120000 per annum
Marlborough
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