Sr. Manufacturing Technician

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Company: Quest Diagnostics

Location: San Juan Capistrano, CA 92675

Description:

Overview

Sr. Manufacturing Technician - San Juan Capistrano, CA - Monday-Friday 8:00AM-5:00PM (Rotational Weekends)

The Sr Manufacturing Technician will be responsible for the manufacturing and in-process testing for IVD products at the San Juan Capistrano facility. Such activities will include among others:
  • Manufacturing of product,
  • troubleshooting,
  • Equipment maintenance
  • metrics trending,
  • execution of validation activities and
  • document creation and revisions

Pay Range: $100,000 - $179,650 / year

Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation.

Benefits Information:
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects - physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include:
Day 1 Medical/Dental/Vision for FT employees who work 30+ hours
15 PTO days first year
Paid Holidays
Annual Bonus Opportunity
401(k) with matching contributions
Variable compensation plan (AIP) bonus
Employee Stock Purchase Plan (ESPP)
Employee Assistance Program (EAP)
Blueprint for Wellness
Tuition Reimbursement for undergraduate and graduate programs for FT employees who work 30+ hours
Opportunities for career advancement
Training provided!

Responsibilities

  • Manufacturing and assembly of IVD products and kits, and coordination of manufacturing schedule for SJC site manufactured products.
  • Creation and revision of label templates in bartender. Implementation of label templates ensuring adequate process controls.
  • Conduct process validation runs as part of commercial manufacturing support.
  • Revision and creation of manufacturing related procedures. Endure adequate and accurate documentation of device history records, instrument records, PM records etc.
  • Support implementation of continuous improvement activities.
  • Execute equipment preventive and corrective maintenance to keep production equipment operational.
  • Help with troubleshooting of problems within the manufacturing process.
  • Create reports and analyze production data / information.
  • Ensure all manufacturing related areas are kept organized and clean and in good housekeeping conditions (inclusive of materials areas)
  • Ensure full compliance with IVD FDA and ISO requirements.
  • Ensure all required training is done on time.


Qualifications

QUALIFICATIONS

Required Work Experience:
  • Minimum of five (5) years' experience in Laboratory and/or Manufacturing

Preferred Work Experience:
  • Minimum of five (5) years' experience in IVD / pharmaceutical or medical device in Manufacturing or Laboratory
  • Laboratory Technician

Physical and Mental Requirements:
  • Prolonged Pipetting and ELISA plate set ups
  • Focused attention
  • Prolonged sitting

Knowledge:
  • FDA and ISO regulations and requirements
  • Quality processes and systems
  • Manufacturing / Laboratory process and systems

Skills:
  • Good record keeping skills
  • Laboratory analytical skills (pipetting, reagents, etc.)
  • Instrumentation skills (plate reader/washers, incubation ovens, shakers, etc.)
  • Analytical and problem-solving skills
  • PC literate (excel, word, Minitab, PowerPoint, etc.)
  • Understand the requirements of a QSRs Quality System. ISO-13485 and GMP environment.


EDUCATION
Associates Degree(Required)
Bachelor's Degree

LICENSECERTIFICATIONS

Quest Diagnostics honors our service members and encourages veterans to apply.

While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume.

2025-84676

EEO

Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets

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