Engineer Process, QC and Calibration Process Development
IDEXX · Westbrook, ME
- Level
- Engineer
- Team
- Quality
- Base pay
- $93k–$98k
- Industry
- Pharma & life sciences
- Posted
- 6 days ago
The role in 30 seconds
An engineer-level quality role at IDEXX (pharma & life sciences) in Westbrook, ME. Hands-on experience with immunoassay techniques (for example, ELISA or similar); reagent preparation and assay troubleshooting experience preferred.
- Tools it names
- DOE, ISO 13485, FDA / GMP
- Base pay
- $93k–$98k
Read from the posting. The full description is below.
From the plant jobs report · week of November 2, 2026
Quality Engineer roles in the US: typical posted base $96k–$135k. This one lists $93k–$98k.
Median of the low and high ends of 555 live postings that list pay, out of 1344 quality engineer openings in the US, read from manufacturers' own careers sites.
Maine plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 1343 other live quality postings in the US.
- Base pay
- About 15% below similar roles
- Experience asked
- Not stated
Typical $94k–$130k, from 516 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- Root cause 68%
- FMEA 39%
- Supplier quality 39%
- Validation (IQ/OQ/PQ) 36%
- Six Sigma 34%
- Lean 33%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at IDEXX
Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
This plant: IDEXX in Westbrook
1 other open role at this site.
- Facilities Maintenance Technician - 3rd Shift · Reliability · Technician
Full description from IDEXXAs posted on their careers site.ShowHide
In this role
- ◆Prepares materials, performs immunoassay experiments, gathers data, carries out analysis and reaches conclusions. Leads DoEs.
- ◆Evaluates assay performance, including signal response, calibration, sensitivity and specificity, reproducibility, and lot-to-lot consistency, using JMP for statistical analysis, data visualization and experimental design. Recommends next steps.
- ◆Prepares and qualifies assay components. May produce and/or test reagents and final products and perform other production-related activities.
- ◆Documents experiments and other lab or production activities in accordance with Good Documentation Practices. Prepares reports and summaries, presents results and conclusions, and maintains appropriate records.
- ◆Participates on and may manage teams, planning and organizing team activities. Leads straightforward projects with small scopes.
- ◆Collaborates and communicates with Manufacturing, Quality Control, Quality Assurance, Product Support and R&D colleagues to support investigations and change orders, exchange information and ensure efficient processes.
- ◆Orders and maintains equipment and work area, including routine instrument maintenance and troubleshooting.
- ◆Provides guidance within areas of direct expertise and may coach or mentor less experienced colleagues.
- ◆Maintains knowledge of products and procedures, developments in the field and industry, and the regulatory environment. Adheres to appropriate procedures and regulatory requirements.
Show full description ↓Show less ↑
As a Process Engineer II (QC and Calibration Process Development), you will support the development, qualification, and continuous improvement of the quality control and calibration processes of immunoassay and PCR-based assays, reagents, and manufacturing processes at our Westbrook, Maine location. Participates on a technically focused team to define technical solutions, exercising consistent discretion and judgment. Executes experiments and follows standard protocols at the laboratory bench to inform decisions or recommendations on assay performance, calibration and process changes. Uses advanced knowledge and statistical tools such as JMP to analyze, interpret and draw conclusions from varying data and circumstances. Prepares solutions, reagents and immunoassay materials, including antigens, antibodies, conjugates and bead-based components. Communicates and presents to colleagues and cross-functional partners.
to succeed
- •Hands-on experience with immunoassay techniques (for example, ELISA or similar); reagent preparation and assay troubleshooting experience preferred.
- •Laboratory bench and instrumentation skills, including routine instrument maintenance and troubleshooting.
- •Analytical and problem-solving skills, including proficiency in JMP for statistical analysis, data visualization and design of experiments. JSL scripting is a plus.
- •Ability to design and run experiments, interpret results and make sound, evidence-based recommendations.
- •Strong documentation skills with a focus on accuracy, traceability and compliance with Good Documentation Practices.
- •Strong communication skills, both verbal and written.
- •Ability to work independently and cooperatively as part of a team.
- •Organizational skills and ability to plan work and manage multiple priorities.
- •Takes initiative and is accountable (shows ownership); focuses on task at hand; detail oriented.
- •Adaptable.
- •Familiarity with quality systems such as ISO 13485 or GMP is preferred.
What You Can Expect From Us
- •Salary rate targeting $93,000 - 98,000 annually (based on experience)
- •Opportunity for performance based annual merit increase
- •Health / Dental / Vision Benefits available day one of employment
- •Opportunity for annual cash bonus
- •5% matching 401k
- •Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more!
Schedule
- •This is a hybrid role based out of our Westbrook, ME corporate headquarters, with a minimum expectation of 3 days a week onsite.
- •Reliable and dependable attendance is an essential function of the position.