Manufacturing Automation Engineer

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.

Job Title: Manufacturing Automation Engineer

Location: Portsmouth, NH 03801

Duration: 6 Months

Job Type: Temporary Assignment

Work Type: Onsite – Some flexibility

Shift: Regular Shift

Pay Rate: $60 to $65

Summary

We are seeking an experienced Automation/Controls Engineer to support manufacturing operations through technical assistance related to manufacturing and process automation systems. The role focuses on ensuring instrumentation and automation systems are designed and operated to meet production needs while supporting process improvements, equipment reliability, compliance, and cross-functional manufacturing activities.

Responsibilities

• Support manufacturing operations through technical assistance for manufacturing and process automation systems.
• Ensure instrumentation and automation systems are designed and operated to meet production needs.
• Plan and execute plant projects involving complex equipment changes and significant process improvements.
• Serve as the Controls lead for technology transfer activities.
• Support the resolution of equipment breakdowns and quality issues in manufacturing suites.
• Provide subject matter expertise to Manufacturing and other departments for the design and operation of process automation equipment.
• Troubleshoot manufacturing equipment and process automation systems, including PI data analysis and code review/troubleshooting, during business hours and as part of an on-call rotation.
• Perform all work safely and complete all required training.
• Participate in IPT/JPT and other meetings as the Controls representative.
• Participate in audits and inspections as the Controls SME when required.
• Own and execute CAPA actions.
• Initiate change controls and participate in all aspects of the change control process.
• Review SOPs, Functional Specifications, and work instructions.
• Maintain all assigned training requirements.
• Perform other duties as assigned.
• May provide direction to 1–2 contractors working on projects within the group.
• May monitor project timelines and budgets to ensure deliverables are completed on time and within budget.

Required Qualifications

• Bachelor's degree in an applicable Engineering field or Computer Science.
• 5–10 years of experience in Pharmaceutical, Biotechnology, or equivalent industrial automation.
• Supervisory and/or project management experience preferred.
• Experience supporting manufacturing and process automation systems.
• Knowledge of instrumentation, automation, and process control systems.
• Experience with troubleshooting manufacturing equipment and automation systems.
• Experience with PI data analysis and code review/troubleshooting.
• Experience with CAPA and Change Control processes.
• Ability to review SOPs, Functional Specifications, and work instructions.
• Strong critical thinking and logical problem-solving skills.
• Proficiency with Microsoft Office Suite, including Outlook, Word, and Excel.
• Ability to prioritize multiple assignments and lead work to successful completion.
• Strong collaboration and communication skills with cross-functional teams.
• Ability to manage internal and external customer relationships professionally.
• Demonstrated integrity, accountability, and commitment to continuous improvement.
• Ability to promote change and support the development of team members.
• Knowledge of cGMP requirements and compliance in API manufacturing.
• Commitment to workplace safety, health and safety procedures, and regulatory compliance.
• Ability to work safely with manufacturing equipment and recognize potential hazards.

TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.