Medical Device Lab Technologist

We need to output HTML fragment with sections: h3 headings for sections present: About the role (maybe from description), Responsibilities, Requirements (or Qualifications), Skills, Benefits, Pay, Schedule. We must not repeat job title. Must preserve all substantive info, remove boilerplate, navigation, legal, EEO, etc. Also remove application instructions, deadline, etc. Also remove "Job Type & Location", "Workplace Type", "Application Deadline", "About Actalent", etc. Also remove "Pay And Benefits" but we need to include Pay and Benefits sections if they have content. The posting includes pay range and benefits details. So we need a Pay section with the range, and Benefits section with listed benefits. Also schedule: "The typical schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., in an hourly position." So schedule section. We also need About the role: The first paragraph after Job Description: "The Quality Control Technician supports process and product quality by preparing equipment, samples, and materials for testing, conducting environmental monitoring in cleanrooms, and reviewing batch records from production. This role also partners with third-party testing laboratories to prepare devices for sterilization, interpret sterility data, and contribute to investigations of non-conformances. You play a key role in ensuring products meet strict quality and regulatory standards in a dynamic, small-company environment." That's substantive. Responsibilities: list of bullet points. We need to extract each responsibility line. They are currently sentences separated by periods but many are run-on. We'll split into list items. Must preserve all info. Let's list them: - Perform environmental monitoring of cleanrooms, including humidity and temperature checks and verification of pest control measures. - Collect, prepare, and submit samples to various internal and external laboratories for further analysis. - Verify and analyze test results to ensure they meet established specifications and quality system requirements. - Prepare and mix chemical formulations for production and manufacturing use in accordance with SOPs. - Execute in-process quality control tasks to monitor product and process performance during manufacturing. - Maintain accurate maintenance records for all equipment used in quality control and production support. - Perform daily pre-operational quality control checks of passivation chemistry to ensure proper performance. - Conduct package visual inspections, seal strength testing, and integrity testing for sterile seals and pouching. - Review sterilization certificates to determine readiness for full product release. - Maintain accurate, complete, and organized records of all quality control activities and findings. - Participate in quality control investigations and corrective and preventive actions (CAPAs) related to non-conformances. - Verify that quality control measurements are accurate and document results with strong attention to detail. - Ensure inspections are completed on time and aligned with production priorities and schedules. - Review manufacturing records, including sterile processing data, test results, certifications, labeling, and paperwork to confirm compliance with specifications and quality system requirements. - Perform batch record review for production lots to ensure completeness, accuracy, and adherence to procedures. - Collaborate with third-party sterilization and contract testing laboratories by preparing devices for sterilization and entering sterility data into documentation systems. - Support investigations by analyzing data from non-conformances and assisting in the development of investigation plans. - Follow standard operating procedures consistently and escalate quality concerns when something appears out of scope. That's all. Requirements / Qualifications: The posting has "Essential Skills" list and "Additional Skills & Qualifications". We need to decide which heading to use. The instruction: Use headings for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). We can combine Requirements and Qualifications maybe as one section? But they said prefer few substantive sections over many thin ones. We could have a "Qualifications" section that includes both essential and additional skills. Or we could have "Skills" section for essential skills and "Qualifications" for additional? However they said use headings like Skills, Benefits, Pay, Schedule. So we likely need a Skills section for essential skills, and maybe Qualifications for additional? But they said "Prefer a few substantive sections over many thin ones." So maybe combine essential and additional into one "Qualifications" section. But they also have a separate "Skills" heading example. Let's think: The posting has "Essential Skills" and "Additional Skills & Qualifications". Could treat "Essential Skills" as Skills section, and "Additional Skills & Qualifications" as Qualifications section. That yields two sections. That's okay. We must not include filler like "commensurate with experience". None present. We need to output only HTML fragment, no html/body tags. Thus:

About the role

...

Responsibilities

• ...
...

Skills

• Associates or Bachelor’s degree in a science-related discipline.
• At least 2 years of experience in a regulated industry such as medical device, pharmaceutical, or food.
• Demonstrated quality mindset and willingness to speak up when issues or out-of-scope activities are identified.
• Proven ability to follow standard operating procedures (SOPs), verified through references.
• Experience in quality control or quality assurance within a regulated environment.
• Hands-on experience with environmental monitoring in cleanrooms.
• Knowledge of microbiology principles and laboratory practices relevant to product and process testing.
• Understanding of Good Manufacturing Practices (GMP) and their application in daily work.
• Experience with sterilization processes and working with sterile products or environments.
• Ability to apply aseptic techniques when handling materials and samples.
• Experience supporting or executing corrective action plans and CAPAs.
• Strong investigation and analysis skills for evaluating non-conformances and quality issues.
• High attention to detail in documentation, record-keeping, and data entry.
• Ability to maintain accurate equipment maintenance and quality records.
• Capability to prepare and mix chemical formulations safely and accurately.
• Comfort working in both cleanroom and production environments and transitioning between hands-on and documentation tasks.

Qualifications

• Experience in the medical device industry.
• Experience working with third-party sterilization laboratories or contract testing labs.
• At least 6 months of sterilization or environmental monitoring experience in a regulated environment such as medical device, pharmaceutical, food, brewery, or aerospace.
• References who can speak to your commitment to quality and adherence to SOPs.
• Interest in career advancement within Quality and willingness to grow into more quality roles over time.
• Ability to wear multiple hats and support various quality and production-related activities in a small, collaborative organization.

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• Life insurance
• 401K with company match of up to 4%
• Profit sharing

Pay

The pay range for this position is $52,000.00 - $62,400.00 per year.

Schedule

The typical schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., in an hourly position.

We also need to include Work Environment? Not required heading but could be included as a paragraph under About the role? The instruction: include a section ONLY when the posting has real, specific content for it — never emit a heading followed by filler/placeholder text. Work Environment has content: "This role is fully on-site and split approximately 50% between cleanroom/production floor activities and 50% documentation and computer-based work. You work in a small, family-run company culture where collaboration, training, and cross-functional support are highly valued. The organization operates across multiple locations and maintains a close-knit team at the local site, with about 55 colleagues. You can expect a strong focus on training for new hires, opportunities to assist in different areas of the business, and potential for career advancement within the Quality function. The typical schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., in an hourly position. Cleanroom and production work may require appropriate gowning or protective attire consistent with regulated manufacturing and sterile processing environments." We already used schedule in its own section; we could incorporate work environment details into About the role or a separate section like "Work Environment". Since we have a schedule section already, we could still have a Work Environment section for the rest. The instruction: Prefer a few substantive sections over many thin ones. Adding Work Environment may be okay if it's substantive. But we already have schedule separate; we could merge schedule into Work Environment. However schedule is a specific heading they listed as possible. We could keep schedule separate and incorporate other work environment details into About the role or a new "Work Environment" section. Let's see: About the role currently only has the first paragraph. We could expand About the role to include work environment details (except schedule). That would keep sections fewer. Let's do that: About the role paragraph includes the description plus work environment details (excluding schedule). Then schedule separate. Thus About the role paragraph: combine: "The Quality Control Technician supports process and product quality by preparing equipment, samples, and materials for testing, conducting environmental monitoring in cleanrooms, and reviewing batch records from production. This role also partners with third-party testing laboratories to prepare devices for sterilization, interpret sterility data, and contribute to investigations of non-conformances. You play a key role in ensuring products meet strict quality and regulatory standards in a dynamic, small-company environment. This role is fully on-site and split approximately 50% between cleanroom/production floor activities and 50% documentation and computer-based work. You work in a small, family-run company culture where collaboration, training, and cross-functional support are highly valued. The organization operates across multiple locations and maintains a close-knit team at the local site, with about 55 colleagues. You can expect a strong focus on training for new hires, opportunities to assist in different areas of the business, and potential for career advancement within the Quality function. Cleanroom and production work may require appropriate gowning or protective attire consistent with regulated manufacturing and sterile processing environments." That seems good. Now schedule section separate. Now ensure we removed all boilerplate: Job Title line, Job Description heading, Job Type & Location, Workplace Type, Application Deadline, About Actalent, EEO, etc. Also removed "Pay And Benefits" heading but we kept Pay and Benefits sections. Check for any leftover like "Job Type & Location This is a Permanent position based out of Saint Paul, MN." That's location info; we might want to include location somewhere? The instruction: do NOT put Job ID / requisition numbers as headings — fold minor metadata into a short

or drop it. Location is minor metadata; we could fold into a short p maybe under About the role or separate? But they said we can drop it. However location is substantive? It's location of job. Might be considered minor metadata; we could include a short p after About the role? But they said "fold minor metadata into a short

or drop it." So we could include a short p with location. But we already have many sections; adding a location p may be okay. However they said prefer few substantive sections over many thin ones. Adding a separate location section would be thin. Better to fold location into About the role paragraph as a short sentence. Let's add at end: "The position is based in Saint Paul, MN." That's minor metadata but we can incorporate. Thus About the role paragraph ends with that sentence. Now check for any other minor metadata like "Job Type & Location This is a Permanent position based out of Saint Paul, MN." Also "Workplace Type This is a fully onsite position in Saint Paul,MN."