Quality Technician, 2nd Shift
for each heading. Use - for any list of duties/requirements/benefits, and
for prose. Do NOT repeat job title as heading. Do NOT put Job ID/requisition numbers as headings. Remove boilerplate. Include only sections with real specific content. Must preserve all substantive info.
We need to parse the posting.
Key info:
- Department: Quality
- Reports to: Quality Engineering Manager
- Work location: On-site, Eden Prairie, Minnesota
- Schedule: Monday through Thursday, 10 hour shifts, 3:00 PM to 2:30 AM
- Pay range: $28.00 to $32.00 per hour
- Position type: Full time, second shift
About Elucent Medical: description.
About The Role: description.
What you will do: list of duties.
What you bring: Education and experience, Skills And Abilities.
Work environment: notes.
Where this role can lead: maybe not needed? Could be part of "About the role" or separate? Not required headings.
Benefits: list.
Affirmative action and equal opportunity: boilerplate to remove.
Also note: "Please note that this job description is not designed to cover..." remove.
We need sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule.
We need to decide what goes where.
- About the role: could be the paragraph "About The Role" plus maybe description of role.
- Responsibilities: list of duties from "What you will do".
- Requirements: maybe education and experience? Could be "What you bring Education and experience".
- Qualifications: maybe ISO etc? Could be overlapping. But we need to follow instruction: include a section only when posting has real specific content for it. We can decide to put Education/Experience under Requirements, and Skills under Skills section. Qualifications maybe we can combine with Requirements? But we need separate headings if content exists. The posting has "Education and experience" and "Skills And Abilities". Also "Work environment". Could treat "Work environment" as part of Requirements? Not sure.
We have to avoid filler. We'll include sections: About the role, Responsibilities, Requirements (education/experience), Skills (skills and abilities), Benefits, Pay, Schedule. Possibly also Qualifications if we have distinct content like ISO etc. But we could put ISO under Requirements as well. Let's see: The posting includes "Education and experience High school diploma plus two years of relevant medical device or ISO 13485 experience, or a two year degree. ISO 13485 experience preferred. ISO 9001 experience is acceptable. Electronics manufacturing knowledge preferred, along with solid electrical and mechanical testing technique. Familiarity with an electronic quality management system is a plus." That's qualifications. Then "Skills And Abilities" list.
Thus we can have Requirements (education/experience) and Qualifications (preferred experience, knowledge). But the instruction says prefer a few substantive sections over many thin ones. Could combine Requirements and Qualifications into one section? But headings are predefined; we must use those headings if we include them. We could include both Requirements and Qualifications if they have content. That's okay.
We also need Pay and Schedule sections.
We must not include filler like "commensurate with experience". Not present.
We need to output only HTML fragment.
Let's craft:
About the role
... paragraph from About The Role and maybe Elucent Medical description? Actually About Elucent Medical is separate but could be part of About the role? The heading "About the role" likely corresponds to the "About The Role" section. We'll put that paragraph.
Then maybe also include a brief about Elucent Medical? Could be part of About the role? But the instruction says use heading for section headings e.g. About the role, Responsibilities, etc. So we can put the Elucent Medical description under About the role? Might be okay. But we have separate "About Elucent Medical" earlier. Could treat that as part of About the role? Might be duplication. However we need to preserve all substantive info. So we need to include that description somewhere. Could put it under About the role as well, or maybe under a separate section like "About the company" but not in allowed headings. Since only allowed headings are those, we could incorporate it into About the role.
Thus About the role: combine Elucent Medical description and About The Role paragraph.
Let's extract:
Elucent Medical is a medical device company building surgical navigation technology for cancer surgery. Their systems turn standard surgical instruments into smart tools, so surgeons can locate and remove tissue with far more precision. Better precision leads to better outcomes for patients, which is the whole point of the work. Capital equipment is manufactured on-site in Eden Prairie. Disposables are produced off-site by a contract manufacturer. The product you inspect on this shift is the equipment that ends up in operating rooms.
About The Role: The Quality Technician on second shift keeps product moving and keeps it correct. You will handle receiving inspection, in-process and final inspection, electrical testing, and the documentation that has to be right before anything is released. A significant part of this job is Nonconforming Material Reports. You will initiate them, manage them through to resolution, and work alongside investigators to put corrective solutions in place. Elucent is looking for someone who owns that process from start to finish instead of passing it along. Second shift runs with a smaller crew, and from midnight to 2:00 AM you are the only quality person on site. That setup works well for someone who is comfortable making a call on their own, who asks good questions during the overlap hours, and who builds enough trust with the team that people know the answer is solid. Specific test procedures can be taught, so you do not need to walk in knowing them. Follow-through is the part that has to come with you.
We'll combine.
Responsibilities: list from "What you will do":
- Perform receiving inspection and preventative maintenance testing.
- Run electrical testing with a multimeter and inspect circuit boards.
- Specific test procedures can be taught on the job.
- Initiate and manage Nonconforming Material Reports, then partner with investigators to follow up and implement corrective solutions.
- Perform in-process and final inspection on components, sub-assemblies, and finished product.
- Review and approve job travelers, also known as Device History Records, before product release.
- Support administration of the electronic quality management system.
- Support quality systems documentation, procedure writing, and customer audit preparation as assigned.
We'll put each as
- .
Requirements: Education and experience:
- High school diploma plus two years of relevant medical device or ISO 13485 experience, or a two year degree.
We could also note ISO 13485 experience preferred, ISO 9001 acceptable, electronics manufacturing knowledge preferred, solid electrical and mechanical testing technique, familiarity with electronic quality management system a plus. Those could be qualifications.
Thus Requirements: maybe just the base education/experience.
Qualifications: Preferred qualifications:
- ISO 13485 experience preferred.
- ISO 9001 experience acceptable.
- Electronics manufacturing knowledge preferred, along with solid electrical and mechanical testing technique.
- Familiarity with an electronic quality management system is a plus.
We'll list.
Skills And Abilities: list:
- Strong math and technical skills.
- Comfortable with MS Office.
- Self-directed and confident working independently.
- Takes initiative without being prompted.
- Builds trust with the team.
- Strong written and verbal communication.
- Comfortable working cross-functionally with peers, customers, and suppliers.
- Steady attention to detail.
We'll list.
Benefits: list:
- Medical, dental, and vision insurance.
- 401(k) with a 4 percent company match.
- Paid holidays, paid vacation, and paid sick time.
- Short term disability and long term disability.
- Life insurance.
- Pet insurance.
- Employee assistance program.
Pay: $28.00 to $32.00 per hour.
Schedule: Monday through Thursday, 10 hour shifts, 3:00 PM to 2:30 AM.
We also have position type full time, second shift; could be included in Schedule or Pay? Maybe include in Schedule section as note. But we have schedule defined; we can add "Full time, second shift" as part of schedule description.
Work location: On-site, Eden Prairie, Minnesota. Could be included in About the role? Or maybe we add a short paragraph under About the role? Could add a sentence.
We need to preserve all substantive info. So include location somewhere. Could add a
under About the role: "Work location: On-site, Eden Prairie, Minnesota."
Also department and reports to maybe not needed but could be included in About the role.
We'll include them in About the role paragraph.
Now ensure we don't include boilerplate: remove Affirmative action etc.
Now output HTML.
Let's craft:
About the role
Elucent Medical is a medical device company building surgical navigation technology for cancer surgery. Their systems turn standard surgical instruments into smart tools, so surgeons can locate and remove tissue with far more precision. Better precision leads to better outcomes for patients, which is the whole point of the work. Capital equipment is manufactured on-site in Eden Prairie. Disposables are produced off-site by a contract manufacturer. The product you inspect on this shift is the equipment that ends up in operating rooms. The Quality Technician on second shift keeps product moving and keeps it correct. You will handle receiving inspection, in-process and final inspection, electrical testing, and the documentation that has to be right before anything is released. A significant part of this job is Nonconforming Material Reports. You will initiate them, manage them through to resolution, and work alongside investigators to put corrective solutions in place. Elucent is looking for someone who owns that process from start to finish instead of passing it along. Second shift runs with a smaller crew, and from midnight to 2:00 AM you are the only quality person on site. That setup works well for someone who is comfortable making a call on their own, who asks good questions during the overlap hours, and who builds enough trust with the team that people know the answer is solid. Specific test procedures can be taught, so you do not need to walk in knowing them. Follow-through is the part that has to come with you. Work location: On-site, Eden Prairie, Minnesota. Department: Quality. Reports to: Quality Engineering Manager.
Then Responsibilities:
Responsibilities
- Perform receiving inspection and preventative maintenance testing.
- Run electrical testing with a multimeter and inspect circuit boards.
- Specific test procedures can be taught on the job.
- Initiate and manage Nonconforming Material Reports, then partner with investigators to follow up and implement corrective solutions.
- Perform in-process and final inspection on components, sub-assemblies, and finished product.
- Review and approve job travelers, also known as Device History Records, before product release.
- Support administration of the electronic quality management system.
- Support quality systems documentation, procedure writing, and customer audit preparation as assigned.
Requirements:
Requirements
- High school diploma plus two years of relevant medical device or ISO 13485 experience, or a two‑year degree.
Qualifications:
Qualifications
- ISO 13485 experience preferred.
- ISO 9001 experience acceptable.
- Electronics manufacturing knowledge preferred, along with solid electrical and mechanical testing technique.
- Familiarity with an electronic quality management system is a plus.
Skills:
Skills
- Strong math and
for prose. Do NOT repeat job title as heading. Do NOT put Job ID/requisition numbers as headings. Remove boilerplate. Include only sections with real specific content. Must preserve all substantive info. We need to parse the posting. Key info: - Department: Quality - Reports to: Quality Engineering Manager - Work location: On-site, Eden Prairie, Minnesota - Schedule: Monday through Thursday, 10 hour shifts, 3:00 PM to 2:30 AM - Pay range: $28.00 to $32.00 per hour - Position type: Full time, second shift About Elucent Medical: description. About The Role: description. What you will do: list of duties. What you bring: Education and experience, Skills And Abilities. Work environment: notes. Where this role can lead: maybe not needed? Could be part of "About the role" or separate? Not required headings. Benefits: list. Affirmative action and equal opportunity: boilerplate to remove. Also note: "Please note that this job description is not designed to cover..." remove. We need sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what goes where. - About the role: could be the paragraph "About The Role" plus maybe description of role. - Responsibilities: list of duties from "What you will do". - Requirements: maybe education and experience? Could be "What you bring Education and experience". - Qualifications: maybe ISO etc? Could be overlapping. But we need to follow instruction: include a section only when posting has real specific content for it. We can decide to put Education/Experience under Requirements, and Skills under Skills section. Qualifications maybe we can combine with Requirements? But we need separate headings if content exists. The posting has "Education and experience" and "Skills And Abilities". Also "Work environment". Could treat "Work environment" as part of Requirements? Not sure. We have to avoid filler. We'll include sections: About the role, Responsibilities, Requirements (education/experience), Skills (skills and abilities), Benefits, Pay, Schedule. Possibly also Qualifications if we have distinct content like ISO etc. But we could put ISO under Requirements as well. Let's see: The posting includes "Education and experience High school diploma plus two years of relevant medical device or ISO 13485 experience, or a two year degree. ISO 13485 experience preferred. ISO 9001 experience is acceptable. Electronics manufacturing knowledge preferred, along with solid electrical and mechanical testing technique. Familiarity with an electronic quality management system is a plus." That's qualifications. Then "Skills And Abilities" list. Thus we can have Requirements (education/experience) and Qualifications (preferred experience, knowledge). But the instruction says prefer a few substantive sections over many thin ones. Could combine Requirements and Qualifications into one section? But headings are predefined; we must use those headings if we include them. We could include both Requirements and Qualifications if they have content. That's okay. We also need Pay and Schedule sections. We must not include filler like "commensurate with experience". Not present. We need to output only HTML fragment. Let's craft:
About the role
... paragraph from About The Role and maybe Elucent Medical description? Actually About Elucent Medical is separate but could be part of About the role? The heading "About the role" likely corresponds to the "About The Role" section. We'll put that paragraph. Then maybe also include a brief about Elucent Medical? Could be part of About the role? But the instruction says use heading for section headings e.g. About the role, Responsibilities, etc. So we can put the Elucent Medical description under About the role? Might be okay. But we have separate "About Elucent Medical" earlier. Could treat that as part of About the role? Might be duplication. However we need to preserve all substantive info. So we need to include that description somewhere. Could put it under About the role as well, or maybe under a separate section like "About the company" but not in allowed headings. Since only allowed headings are those, we could incorporate it into About the role. Thus About the role: combine Elucent Medical description and About The Role paragraph. Let's extract: Elucent Medical is a medical device company building surgical navigation technology for cancer surgery. Their systems turn standard surgical instruments into smart tools, so surgeons can locate and remove tissue with far more precision. Better precision leads to better outcomes for patients, which is the whole point of the work. Capital equipment is manufactured on-site in Eden Prairie. Disposables are produced off-site by a contract manufacturer. The product you inspect on this shift is the equipment that ends up in operating rooms. About The Role: The Quality Technician on second shift keeps product moving and keeps it correct. You will handle receiving inspection, in-process and final inspection, electrical testing, and the documentation that has to be right before anything is released. A significant part of this job is Nonconforming Material Reports. You will initiate them, manage them through to resolution, and work alongside investigators to put corrective solutions in place. Elucent is looking for someone who owns that process from start to finish instead of passing it along. Second shift runs with a smaller crew, and from midnight to 2:00 AM you are the only quality person on site. That setup works well for someone who is comfortable making a call on their own, who asks good questions during the overlap hours, and who builds enough trust with the team that people know the answer is solid. Specific test procedures can be taught, so you do not need to walk in knowing them. Follow-through is the part that has to come with you. We'll combine. Responsibilities: list from "What you will do": - Perform receiving inspection and preventative maintenance testing. - Run electrical testing with a multimeter and inspect circuit boards. - Specific test procedures can be taught on the job. - Initiate and manage Nonconforming Material Reports, then partner with investigators to follow up and implement corrective solutions. - Perform in-process and final inspection on components, sub-assemblies, and finished product. - Review and approve job travelers, also known as Device History Records, before product release. - Support administration of the electronic quality management system. - Support quality systems documentation, procedure writing, and customer audit preparation as assigned. We'll put each as
under About the role: "Work location: On-site, Eden Prairie, Minnesota." Also department and reports to maybe not needed but could be included in About the role. We'll include them in About the role paragraph. Now ensure we don't include boilerplate: remove Affirmative action etc. Now output HTML. Let's craft:
About the role
Elucent Medical is a medical device company building surgical navigation technology for cancer surgery. Their systems turn standard surgical instruments into smart tools, so surgeons can locate and remove tissue with far more precision. Better precision leads to better outcomes for patients, which is the whole point of the work. Capital equipment is manufactured on-site in Eden Prairie. Disposables are produced off-site by a contract manufacturer. The product you inspect on this shift is the equipment that ends up in operating rooms. The Quality Technician on second shift keeps product moving and keeps it correct. You will handle receiving inspection, in-process and final inspection, electrical testing, and the documentation that has to be right before anything is released. A significant part of this job is Nonconforming Material Reports. You will initiate them, manage them through to resolution, and work alongside investigators to put corrective solutions in place. Elucent is looking for someone who owns that process from start to finish instead of passing it along. Second shift runs with a smaller crew, and from midnight to 2:00 AM you are the only quality person on site. That setup works well for someone who is comfortable making a call on their own, who asks good questions during the overlap hours, and who builds enough trust with the team that people know the answer is solid. Specific test procedures can be taught, so you do not need to walk in knowing them. Follow-through is the part that has to come with you. Work location: On-site, Eden Prairie, Minnesota. Department: Quality. Reports to: Quality Engineering Manager.
Then Responsibilities:Responsibilities
- Perform receiving inspection and preventative maintenance testing.
- Run electrical testing with a multimeter and inspect circuit boards.
- Specific test procedures can be taught on the job.
- Initiate and manage Nonconforming Material Reports, then partner with investigators to follow up and implement corrective solutions.
- Perform in-process and final inspection on components, sub-assemblies, and finished product.
- Review and approve job travelers, also known as Device History Records, before product release.
- Support administration of the electronic quality management system.
- Support quality systems documentation, procedure writing, and customer audit preparation as assigned.
Requirements
- High school diploma plus two years of relevant medical device or ISO 13485 experience, or a two‑year degree.
Qualifications
- ISO 13485 experience preferred.
- ISO 9001 experience acceptable.
- Electronics manufacturing knowledge preferred, along with solid electrical and mechanical testing technique.
- Familiarity with an electronic quality management system is a plus.
Skills
- Strong math and