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Senior Automation Technician - Equipment 2nd Shift
12500 Whitewater Drive, Minnetonka, MN 55343 US
Job Description
POSITION SUMMARY:
The Sr Automation Technician will be responsible for setup, troubleshooting and operating manufacturing equipment and providing technical support throughout products lifecycle from product development through commercial production.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
These may include but are not limited to:
- Lead the technical manufacturing process to include setup, calibrating and operating automated equipment.
- Optimize manufacturing process to minimize equipment downtime
- Monitor and troubleshoot processes and machines.
- Work with Engineers to design, build, and test solutions to a variety of technical problems.
- Collect data and write daily reports for Engineering and Production.
- Run diagnostics and calibrate equipment, perform engineering tests, and support equipment functionality as needed.
- Conduct experiments and investigations in collaboration with Engineers.
- Order technical components and spare parts for equipment.
- Provide guidance and training to the manufacturing team.
- Support continuous improvement efforts by offering suggestions and evaluating processes
- Maintain records and assist with production assembly.
- Assist in PM and maintenance activities.
- Internal and external relationships
- Other duties as assigned
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES:
- High School diploma or equivalent, and trade school certification, specialized training/apprenticeship and/or equivalent experience in high volume manufacturing automation. Engineering or Automation technician certification preferred.
- 6+ years of experience in automated manufacturing, with experience in the medical device or pharmaceutical industry preferred.
- 3+ years of experience working with automation and packaging equipment.
- An equivalent combination of experience and education may be considered
- Technical, equipment, and software knowledge is necessary
- Background in industrial controls and PLCs with working knowledge in robotics and/or mechanical components.
- Strong knowledge of Good Documentation (GDP) and current Good Manufacturing (GMP) Practices are required.
- Critical understanding of the importance of documentation and data traceability.
- Experience in medical device, pharmaceutical, GMP, or regulated industry
- Experience with process validation (IQ/OQ/PQ)
- Experience with Lean principles and metrics, problem solving methodologies, DMAIC, SPC, process capability analysis.
- Ability to contribute engineering support to technical plans and reports.
- Experience with developing, validating, operating, and troubleshooting automated assembly and packaging/cartoning equipment.
- Familiarity with Drug Supply Chain Security Act (DSCSA) and serialization.
- Demonstrated experience in the training and development of employees in a manufacturing environment.
- Excellent organizational skills.
- Must be able to work well independently and in a team environment.
- Demonstrated experience in performing product and/or process investigations.
- Excellent communication skills, both verbal and written.
- Must have the ability to lift 50 pounds.
- Able to perform physical activity such as standing for long periods of time, walking, and working with hands.
- Lead or supervisory experience a plus.
ENVIRONMENTAL CONDITIONS:
Physical Activities: On a continuous basis, be at a desk for a long period of time; intermittently answer the telephone and type on a computer. Some walking and lifting up to 30 lbs. may be required. The noise level in the work environment is usually low to moderate.
The physical requirements described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities of this job.
Laboratory Activities, if applicable: Biology and chemical laboratory environments experience needed. Environmental health and safety requirements also apply.
TRAVEL:
Travel may require up to 5% of your time.
Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
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