Manufacturing Compliance Engineer/Senior Manufacturing Compliance Engineer
$80.5k - $149.5kGenentech
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. #J-18808-Ljbffr Genentech
$95.2k - $176.8k
...PositionThis role is a vital part of our Manufacturing team at Genentech Oceanside, which is... ...worldwide. As a key technical and compliance leader within this department, you will... ...MSAT, Quality Assurance, Facilities & Engineering, and Compliance. In this collaborative...SuggestedFull timeLocal areaWorldwideRelocation package$135k
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DescriptionThe Validation Engineer II is a mid-level role responsible for creating, planning... ..., ensuring quality, timeline, and compliance expectations are met while working alongside... ...guidance from and collaborates with senior validation engineers; may informally assist...Full timeLocal areaVisa sponsorshipWork visa- Genentech is seeking an engineer to join the Oceanside team to resolve technical and compliance issues across Quality, Technology, and Operations while maintaining cGMP and SOP standards. You will review documentation, support tech transfer, and drive continuous improvement...Relocation package
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ResponsibilitiesMaxLinear is seeking a Senior Staff Signal & Power Integrity (SI/PI) Engineer to join our team. In this role, you will focus on the following:Development of state-of-the-art packages and printed circuit boards (PCBs) for MaxLinear’s next generation products...SeniorWork experience placementLive in- ...Validation Engineer IIMain Purpose of the RoleResponsible for creating and implementing... ...implemented for systems and processes used to manufacture, control and store intermediates and... ...production processes and systems in compliance to internal and external requirements...Work experience placement
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...Validation Engineer IIThe Validation Engineer II will support validation activities for GMP manufacturing facilities, utilities, equipment, laboratory systems, and processes within... ...qualification protocols, and maintaining compliance with quality and regulatory requirements....Temporary work$123.93k - $160.38k
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Job Title: Senior Specialist, Mechanical Engineer (Mechanisms) (Sign-On Bonus Available)Job Code: 43469Job... ...standards.Experience in additive manufacturing, part optimization, and design for... ...testing, and manufacturing processesIn compliance with pay transparency requirements...SeniorWork at officeRelocation packageFlexible hours$115k - $140k
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...including reports, conference abstracts, presentations, manuscripts, product collateral.Prepare clear, complete and accurate technical engineering documentation.Responsible for aspects of calibration, safety, maintenance, and efficient utilization of testing equipment to...Full timeLocal areaVisa sponsorshipWork visa$87k - $95k
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...PositionThis role is a key part of our Equipment Engineering team, dedicated to delivering cutting-... ...for Single-use Systems in biologics manufacturing. As a member of this team, you will... ...multidisciplinary teams, and ensuring compliance with industry and regulatory standards...Full timeTemporary workFor contractorsLocal areaRemote workWorldwideRelocation package$80k - $115k
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