Top 5 Compliance engineer Jobs in Carlsbad, Ca

Manufacturing Compliance Engineer/Senior Manufacturing Compliance Engineer
Genentech —Oceanside, CA
- $80,500 - $149,500 a year
- Online Application
- Bachelor of Science
- Mid-level
- Bachelor's degree
2d
Principal Manufacturing Compliance Engineer
Genentech —Oceanside, CA
- $95,200 - $176,800 a year
- Online Application
- 5 years
- Bachelor of Science
- Mentoring
2d
Product Safety & Compliance Engineer
Hunter Industries —San Marcos, CA
- $87,000 - $95,000 a year
- Hybrid work
- Engineering
- English
- Mid-level
- Profit sharing
Quick Apply
Manager, Compliance Engineering - Safety & EMC
Tandem Diabetes Care —San Diego, CA
- $141,800 - $177,300 a year
- Full-time
- Hybrid work
- Background check
- 5 years
- Pass drug screening
- Health savings account
- Employee stock purchase plan
Quick Apply
1d

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compliance engineer jobs near carlsbad, ca

Manufacturing Compliance Engineer/Senior Manufacturing Compliance Engineer

Genentech -
Oceanside, CA

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Job Details

Full-time
$80,500 - $149,500 a year
2 days ago

Qualifications

Resource allocation
Compliance risk assessment
Performance improvement leadership
EHS
Content creation for technical audiences
Quality records maintenance
Defect resolution root cause analysis
Cleanroom environmental monitoring
Calibration
Technical documentation
Bachelor of Science
Preventive action implementation
Safety regulations
Coaching
Technical writing experience within manufacturing
Production deviation management
Engineering process optimization
Operational risk assessment
Quality control preventive actions
Corrective and preventive actions (CAPA)
Cleanroom protocols
Mid-level
Personal protective equipment (PPE) adherence
Manufacturing standard operating procedures
ICH guidelines
Bachelor's degree
Pharmaceutical company experience
Decision making
Technology transfer (scale-up process)
Quality assurance experience within pharmaceutical industry

Full Job Description

The Position

Join our Oceanside team and take on a meaningful role at the heart of biochemical manufacturing. You’ll collaborate across teams to resolve challenges, maintain quality system records, and ensure compliance with regulatory standards using cGMP and SOPs. Your responsibilities will include owning and investigating deviations, supporting tech transfer and commercial manufacturing, reviewing and approving technical documentation, supporting continuous improvements, and partnering with MSAT, Site Operations, and Quality Assurance to tackle quality issues and improve our compliance standing and understanding.

In addition, you’ll lead operational excellence initiatives to improve processes, solve complex problems, and uphold high standards for safety, quality, and compliance. Your contributions will help ensure our products consistently meet customer and regulatory expectations.

This role centers on broader compliance knowledge, with expertise in inspection strategies, risk assessment, and various compliance programs, such as environmental monitoring, personnel flow, and gowning procedures.

The Opportunity

Manage and resolve technical and compliance issues with Quality, Technology, Maintenance, Facilities, Calibration & EH&S.
Solve a wide range of difficult issues that impact multiple functions following cGMP regulations and Genentech standards by applying advanced theory, technical principals and expert judgment.
Troubleshoot and direct the resolution of Quality issues by fostering effective interdepartmental and cross-functional partnership.
Lead and and/or facilitate Root Cause Analysis sessions for more complex issues and serve as a coach and process owner for DMS Event Observer/DO Community within their function on best practices
Be able to act as SME to regulatory agencies
Implement and follow through on corrective and preventative actions (CAPA) in accordance with timelines.

Who you are

Engineer: BS/BA in Life Sciences/Engineering preferred, and 0-2 years of experience in the pharmaceutical, biopharmaceutical industry or a combination of education and experience.
Senior Engineer: BS/BA in Life Sciences/Engineering preferred, and 3-7 years of experience in the pharmaceutical, biopharmaceutical industry or a combination of education and experience.
Ability to make sound decisions about scheduling, allocation of resources and managing of priorities.

Preferred

Strong oral and written communication skills.
Ability to make sound decisions with minimal supervision.
Possess thorough knowledge and understanding of cGMPs and familiarity with FDA, ICH and European guidelines.
Manage assignments that are complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations.
Experience in technical writing, such as, creation and revision of Standard Operating Procedures or other technical reports/evaluations is desirable

Work Environment/Physical Demands/Safety Considerations

Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn.
Work in clean room environment with large mechanical equipment, piping, and pumps connecting to tanks serviced by high-pressure steam, water and air together this creates a load environment.
May work with hazardous materials.

Relocation benefits are available for this posting.

The expected salary range for this position based on the primary location of Oceanside, CA is $80,500 - $149,500 annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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compliance engineer jobs in carlsbad, ca

Manufacturing Compliance Engineer/Senior Manufacturing Compliance Engineer

Principal Manufacturing Compliance Engineer

Product Safety & Compliance Engineer

Manager, Compliance Engineering - Safety & EMC

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