Role at a glance
- Salary
- Not Disclosed
- Location
- San Diego, California, United States
- Employment
- Full-time
- Experience
- 0-2 years experience in quality assurance field in a regulated environment; direct experience working in in-vitro diagnostic...
- Education
- Bachelor's Degree Engineering and/or Science Degree, preferred
- Visa support
- This role is not eligible for visa sponsorship.
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Role Summary
The Mfg/Ops Quality Engineer 1 supports sustaining quality activities in a manufacturing environment, working with Manufacturing and Process Engineering. The role supports product lifecycle quality, validation and transfer activities, and compliance of manufacturing processes and validation programs.
What You'll Do
- Provide ongoing quality engineering support throughout the product life cycle.
- Support validation planning and transfer activities, including helping teams determine validation needs and requirements.
- Review nonconformances and QI/CAPA records, investigations, corrective actions, validation reports, and change orders for adequacy and...
- Support process risk management and coordinate risk-based issue resolution and gap closure.
- Trend, analyze, and report quality data to improve products and processes.
- Collaborate with counterparts and cross-functional teams at other Illumina sites.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
0-2 years of quality assurance experience in a regulated environment. Knowledge and experience applying quality regulations and standards (21CFR 820, ISO 13485, ISO 14971, IVDD). Knowledge and experience with instituting quality controls in an ERP system. Highly effective communication, facilitation, and negotiation skills; adaptable to a fast-paced, dynamic work environment with shifting demands.
Preferred
- Bachelor's Degree Engineering and/or Science Degree.
- Direct experience working in in-vitro diagnostic manufacturing.
- SAP experience for instituting quality controls in an ERP system.
Original job description
Content provided by the employer
Original job description
Content provided by the employer
This position is responsible for manufacturing and product Quality activities. This role is within Mfg/Ops Quality organization and is accountable for supporting day to day sustaining activities in a manufacturing environment. The position requires exceptional communication, interpersonal, and project management skills to effectively coordinate activities and deliver results.
This position will have direct interaction with Manufacturing and Process Engineering groups to support manufacturing sustaining activities, continuous improvement, and manufacturing capacity expansion. The position may also have quality oversight for more than one manufacturing area. The position will be responsible to support change management activities, Nonconformances, equipment lifecycle, meeting facilitation and other ad hoc sustaining manufacturing requests.
Responsibilities:
- Provide ongoing quality engineering support throughout the product life cycle.
- Provide support to engineering and manufacturing functions for validation planning and transfer activities. Assist teams in determining validation needs and requirements.
- Ensures adequacy of non-conformances and QI/CAPA records, investigations, and corrective actions.
- Support process risk management activities and ensure quality and completeness of validation packages and change orders.
- Become familiar with the applicable technology to facilitate participation in technical discussions and risk-based decision making.
- Review verification and validation reports and identify gaps for GMP compliance.
- Develop and execute strategies to close gaps in an efficient, technical, and compliant manner.
- Coordinate issue resolution using a risk-based approach.
- Ensure manufacturing processes and validation programs meet requirements of FDA and ISO.
- Trend, analyze, and report on quality data in order to improve product and process; develop recommendations based on data analysis.
- Collaborate with counterparts and cross-functional teams at other Illumina sites.
- Other activities as assigned.
Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.
Education / Experience:
- Bachelor's Degree Engineering and/or Science Degree, preferred
- 0-2 years experience in quality assurance field in a regulated environment; direct experience working in in-vitro diagnostic manufacturing preferred
- Knowledge and experience applying quality regulations and standards (21CFR 820, ISO 13485, ISO 14971, IVDD)
- Knowledge and experience with instituting quality controls in an ERP system, SAP preferred
- Highly effective communication, facilitation and negotiation skills
- Adaptable to fast-paced, dynamic work environment with shifting demands
We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
About the company
Illumina
Large Enterprise
Illumina is a global leader in genomics, focusing on advancing human health through innovative DNA sequencing and array-based technologies. The company develops an extensive range of products and services that enable researchers and clinicians to unlock the potential of the genome, contributing to areas such as personalized medicine, genetic research, and diagnostics. With a commitment to improving life through genomics, Illumina continuously invests in technology and partnerships to enhance the accessibility and applicability of genetic information in healthcare and research settings.