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San Carlos, California, United States
Actively hiring, first seen by us 4 days agoThe compensation package will be competitive and includes comprehensive benefits and an equity component. Salary Range: $121,000 - $142,000 Relocation:Read the full posting
Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy): Remote Compensation:Read the full posting
Verify data for all commercial regulatory submissions
Build data management and verification workflows that keep process data accurate and traceable
Acquire and technically evaluate process data from internal teams and contract manufacturing sites
Assess process trends and proposed process improvements using engineering knowledge
Build structured systems to capture and retain process knowledge and decision rationales
Lead and own data verification for all commercial regulatory submissions.
Develop data management and verification workflows that preserve the accuracy, integrity, and traceability of manufacturing process data.
Acquire, integrate, and technically evaluate manufacturing process data from internal teams and contract manufacturing sites
Assess process trends and discrepancies using engineering knowledge, and evaluate the technical rationale and potential impact of proposed process improvements
Develop structured systems and workflows to capture and retain organizational knowledge, including protocols, study results, lessons learned, and decision rationales.
Bachelor’s degree in Chemical Engineering, Bioprocess Engineering, or a related engineering discipline is required. 8+ years of relevant experience in biopharmaceutical process engineering, Manufacturing Science and Technology (MSAT), process development, manufacturing technical support, or related engineering work, including at least 3 years in the life sciences or biotechnology industry. Other combinations of education and/or experience may be considered.
Experience supporting clinical trials and regulatory submissions (e.g., IND, BLA).
Experience in scaling systems and processes in a high-growth, early- to mid-stage.
Experience interpreting manufacturing process data and applying engineering and statistical methods to evaluate process performance.
Proven experience leading enterprise data governance and knowledge sharing initiatives in a highly regulated environment.
Experience with tools like SharePoint, Veeva Vault, Confluence, Tableau, and SQL is highly desirable.
Requirements: Bachelor’s degree in Chemical Engineering, Bioprocess Engineering, or a related engineering discipline is required. 8+ years of relevant experience in biopharmaceutical process engineering, Manufacturing Science and Technology (MSAT), process development, manufacturing technical support, or related engineering work, including at least 3 years in the life sciences or biotechnology industry. Other combinations of education and/or experience may be considered. - Experience interpreting manufacturing process data and applying engineering and statistical methods to evaluate process performance.
Actively hiringFirst seen by us 4 days ago, still listed, and not a repost of an earlier posting.
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Day 4
Early. Similar jobs usually come down between day 5 and day 57.
From 607 similar postings that came down. Coming down is not always a hire.
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Open jobs by the week we first saw them, last 12 weeks.
Hiring recordAdd your resume and we’ll mark which of these tools you already use, and point out anything in the posting that could rule you out.
- Strong technical communication, project management, and cross-functional collaboration skills, with the ability to work effectively with engineering, scientific, and manufacturing teams. - Experience with tools like SharePoint, Veeva Vault, Confluence, Tableau, and SQL is highly desirable. Preferred:
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We file this job under Data Governance, by the work the posting describes.
Data governance staff keep a company's data accurate, documented and used within the rules. They agree what key fields mean, set up quality checks, track who owns each dataset and look after master data.
Postings ask for SQL, a governance tool such as Collibra or Informatica, knowledge of privacy and data rules, and a lot of work with other teams.
A data engineer builds the systems that move data; governance staff set and check the standards that data has to meet.
As we grow, we are seeking a strategic and collaborative Process Engineer I, Data and Knowledge Management to ensure the integrity, accessibility, and effective use of data and knowledge assets across the organization. This role will execute component-level analysis, utilizing data and knowledge resources critical to our process development, regulatory, and operational activities. The Process Engineer I, Data and Knowledge Management is instrumental in ensuring scientific data integrity, regulatory readiness, and the preservation of institutional knowledge in a dynamic, fast-paced clinical environment.
Engineering Analytics & Process Insights:
Manufacturing Process Data Management & Governance:
Process Knowledge Management:
Collaboration & Technical Leadership:
Compliance & Risk Management:
Bachelor’s degree in Chemical Engineering, Bioprocess Engineering, or a related engineering discipline is required. 8+ years of relevant experience in biopharmaceutical process engineering, Manufacturing Science and Technology (MSAT), process development, manufacturing technical support, or related engineering work, including at least 3 years in the life sciences or biotechnology industry. Other combinations of education and/or experience may be considered.
Preferred:
Equal Opportunity
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
Recruitment Fraud Notice
Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent Vaxcyte in recruitment activities. Vaxcyte has an established recruitment process for all positions prior to issuing an offer for employment and we will never extend unsolicited employment offers or ask candidates to provide financial or sensitive personal information as part of the application process. All legitimate communication from Vaxcyte will come from an official @vaxcyte.com email address. Qualified and interested candidates should apply to current openings at vaxcyte.com/careers.
Selected passages from the saved posting. Check the full description for conditions and exceptions.
The compensation package will be competitive and includes comprehensive benefits and an equity component. Salary Range: $121,000 - $142,000 Relocation:
San Carlos, California, United States
Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy): Remote Compensation:
No clear work-authorization passage found. Eligibility is unconfirmed.