

New · posted Nov 13
Epredia · Medical Devices
Quality Control Technician II (2nd Shift)
- Portsmouth, NH
- On-site
- Full-time
- Associate & Specialist
The role
Make a Meaningful Impact
Ready to join a team where your work makes a daily difference in healthcare?
Epredia is a global leader in precision cancer diagnostics solutions. In fact, every second, our products are used 48 times in labs and medical facilities around the world.
We are a proud member of PHC Group, a global collection of companies committed to delivering precision technology for the future of healthcare, from specialized medical equipment to health IT systems to research tools.
Who you are: You have energy and drive in abundance, a passion for serving our customers and possess a growth mindset and love of continuous learning, with an appreciation for diverse perspectives and helping others win.
Position Overview: Our values reinforce our culture of collaboration, growth mindset, and how we serve our customers.
- The Quality Control Technician II is responsible for the inspection and disposition of incoming, in-process and finished goods within the site.
What you need
Qualifications & Skills
- High School Diploma or equivalent required with 1+ years of relevant experience.
- Experience managing multiple laboratory tests, projects, or assignments simultaneously.
- Experience working in a fast-paced laboratory, manufacturing, or production environment.
- Experience performing repetitive laboratory procedures in a regulated environment preferred.
- Experience maintaining laboratory records, documentation, or sample tracking preferred.
- Experience documenting laboratory results and procedures in written reports preferred.
- Moderate physical demands including ability to lift up to 25 lbs., bend, reach, climb ladders and stand for extended periods.
What you'll do
- Perform quality inspection (visual or microscopic) of incoming materials, in process and final products, and perform proper reporting or documentation of inspections.
- Execute QC investigations (nonconformance and customer requests).
- Utilize SAP system for resulting out.
- Maintain standards in accordance with GMPs, SOPs, and ISO regulations.
- Understand and exercise all safety requirements and procedures.
- Maintain up-to-date knowledge of all applicable quality regulations, guidelines, and standards.
- Participate in continuous improvement activities on site.
Ready to Make an Impact?
If this opportunity aligns with your skills and career goals, we'd love to hear from you. Apply today and take the next step in your career with us.
Pay and benefits
$41,600 – $52,936 a year
Employer provided$20.00 – $25.45 an hour · yearly at 2,080 hours (40 a week)
How this comparesCompany Benefits
Medical, Dental, and Vision benefits effective on first day of employment
3weeks
Paid Time Off – Eligible to accrue up to 3 weeks of Paid Time Off (PTO), pro-rated based on start date
Paid Holidays
6%
401(K) Retirement Plan – Company Matching Contribution up to 6%
Quarterly Incentive Bonus Plan – eligible to participate to earn additional compensation
90days
Tuition Reimbursement – eligible after 90 days of employment
10%
10% Shift Premium for 2nd Shift
The hiring range for this position is: $20.00-$25.45/hr, plus individuals may be eligible for an annual discretionary bonus. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. Epredia offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation and more.
Where you'll work
Portsmouth, NHOn-siteOpen in Maps (opens in a new tab)
More jobs in Portsmouth, NHEqual opportunity, accessibility and legal noticesEpredia's statements, word for word
Building an Inclusive Culture
We are a company that brings the best people together and leverages their varying backgrounds, ideas, and points of view to invent on behalf of all customers. We are committed to equal employment opportunity for all individuals, without regard to race, color, national origin, ancestry, sex, age, religion, physical or mental disability, medical condition, veteran status, marital status, pregnancy, sexual orientation, gender identity, genetic information, or any other protected classes which may exist under applicable federal, state, or local law.
Job intelligence
The context around this role
Live data · November 13, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% below the US median for Quality Inspection roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US60 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $41,600 | — | $52,936 |
| All US (middle half) | $46,000 | $48,000 | $51,625 |
This role: Epredia's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Inspection roles at the same level on Regulatory Jobs, November 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Inspection
The general path across 105 open Quality Inspection roles on Regulatory Jobs, with the titles they carry most. Not Epredia's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs6
- Lab testing and methods5
- GMP and compliance4
- Collaboration and leadership3
- Investigations and CAPA1
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Inspection work in medical devices, led by the one this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485Named in the posting
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- FDA21 CFR Part 806(official source, opens in a new tab)Reports of medical device corrections and removals
- FDA21 CFR Part 830 (UDI)(official source, opens in a new tab)Unique device identification and the GUDID database
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDA21 CFR Part 801(official source, opens in a new tab)FDA labeling requirements for medical devices
- ISOISO 15223-1(official source, opens in a new tab)Symbols for medical device labels and labeling
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
Company hiring pulse
Epredia on Regulatory Jobs
- 3
- Open roles
- 3
- Distinct roles
- 2
- Locations
By discipline
- Quality3 100%
By level
- Associate & Specialist3 100%
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Quality Control Technician II (2nd Shift) at Epredia
Open until filled. $42K–$53K a year, employer provided.


