Material Sciences Specialist
Novato, CA · On-site
BioMarin is seeking a temporary contractor to support execution of a global material specification ... with Veeva, document management systems, and electronic quality systems. • Ability to ...
Material Sciences Specialist
Novato, CA · On-site
BioMarin is seeking a temporary contractor to support execution of a global material specification ... with Veeva, document management systems, and electronic quality systems. • Ability to ...
Validation Engineer
Thousand Oaks, CA · On-site
$60 - $74/hr
GMP * Engineering * technical writing * validations * veeva * Computer System Validation ... Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one ...
New
Quick apply
Validation Engineer
Thousand Oaks, CA · On-site
$60 - $74/hr
GMP * Engineering * technical writing * validations * veeva * Computer System Validation ... Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one ...
New
Associate Director, Clinical Development Trial Lea
San Diego, CA · On-site
$205K - $217K/yr
Veeva * MS Project * Power BI * Enrollment Strategy & Trial Execution Qualifications * Bachelor ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...
Associate Director, Clinical Development Trial Lea
San Diego, CA · On-site
$205K - $217K/yr
Veeva * MS Project * Power BI * Enrollment Strategy & Trial Execution Qualifications * Bachelor ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...
This role supports priority business needs across the Pain Business Unit through temporary ... Utilize Veeva and other approved systems to document activity, customer interactions, account plans ...
New
This role supports priority business needs across the Pain Business Unit through temporary ... Utilize Veeva and other approved systems to document activity, customer interactions, account plans ...
New
Pharmaceutical Project Coordinator
Vacaville, CA · On-site
$35 - $45/hr
Temporary Assignment Work Type: Onsite Summary: We are seeking a Project Coordinator - Change ... platforms such as Veeva, TrackWise, MasterControl, or similar systems preferred. * Strong ...
Quick apply
Pharmaceutical Project Coordinator
Vacaville, CA · On-site
$35 - $45/hr
Temporary Assignment Work Type: Onsite Summary: We are seeking a Project Coordinator - Change ... platforms such as Veeva, TrackWise, MasterControl, or similar systems preferred. * Strong ...
BioMarin is seeking a temporary contractor to support execution of a global material specification ... with Veeva, document management systems, and electronic quality systems. • Ability to ...
BioMarin is seeking a temporary contractor to support execution of a global material specification ... with Veeva, document management systems, and electronic quality systems. • Ability to ...
This role supports priority business needs across the Pain Business Unit through temporary ... Utilize Veeva and other approved systems to document activity, customer interactions, account plans ...
New
This role supports priority business needs across the Pain Business Unit through temporary ... Utilize Veeva and other approved systems to document activity, customer interactions, account plans ...
New
BioMarin is seeking a temporary contractor to support execution of a global material specification ... Familiarity with Veeva, document management systems, and electronic quality systems. Ability to ...
BioMarin is seeking a temporary contractor to support execution of a global material specification ... Familiarity with Veeva, document management systems, and electronic quality systems. Ability to ...
Temp Veeva information
What is a Temp Veeva?
A Temp Veeva is a temporary employee or contractor who works with Veeva Systems software, which is widely used for cloud-based solutions in the life sciences industry. These professionals typically assist with implementing, managing, or supporting Veeva applications such as Veeva Vault, CRM, or QualityDocs. Temp Veeva workers may be hired for short-term projects, system migrations, or to cover workforce gaps. Their responsibilities can include data entry, system configuration, user support, or training. This role is ideal for individuals with experience in pharmaceutical regulations, software administration, and project management.
What are the key skills and qualifications needed to thrive as a Temp Veeva specialist, and why are they important?
To thrive as a Temp Veeva Specialist, you need a strong understanding of Veeva Vault applications, data management, and relevant industry regulations, typically paired with experience in life sciences or pharmaceuticals. Familiarity with Veeva Vault platforms, document management systems, and possibly certifications such as Veeva Administrator or related credentials is highly valuable. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring data quality and collaborating with cross-functional teams. These skills and qualifications are vital to maintain compliance, streamline processes, and support efficient document and data management in regulated environments.
What are some common challenges Temp Veeva professionals face when working with new teams or clients?
Temp Veeva professionals often face the challenge of quickly adapting to different organizational processes and compliance standards, as each client may have unique configurations of the Veeva platform. Additionally, they must rapidly build rapport with new teams and stakeholders to facilitate smooth onboarding and project execution. Effective communication and a proactive approach to learning the nuances of each environment are essential for overcoming these challenges and delivering value efficiently.
What is the difference between Temp Veeva vs Veeva Administrator?
| Aspect | Temp Veeva | Veeva Administrator |
|---|---|---|
| Certifications | Veeva certifications often preferred | Veeva certifications required |
| Work Environment | Temporary, project-based roles | Full-time, ongoing support roles |
| Industry Usage | Used in clinical, regulatory, commercial projects | Primarily in life sciences companies managing Veeva systems |
Temp Veeva roles are typically short-term, project-focused positions requiring familiarity with Veeva systems, while Veeva Administrator roles are permanent positions involving ongoing system management and support. Both roles demand Veeva certifications and industry experience, but differ mainly in duration and scope of responsibilities.
What are the most commonly searched types of Veeva jobs in California?
The most popular types of Veeva jobs in California are:
What are popular job titles related to Temp Veeva jobs in California?
For Temp Veeva jobs in California, the most frequently searched job titles are:
What job categories do people searching Temp Veeva jobs in California look for?
The top searched job categories for Temp Veeva jobs in California are:
What cities in California are hiring for Temp Veeva jobs?
Cities in California with the most Temp Veeva job openings:
Material Sciences Specialist
Novato, CA • On-site
Talent Software Services, Inc
Other
Posted 20 days ago
Job description
Position Summary:
BioMarin is seeking a temporary contractor to support execution of a global material specification remediation program associated with regulatory commitments and CAPA activities. The contractor will work closely with Material Sciences, Global Quality, Regulatory Compliance, and Site Quality teams to review, revise, implement, and maintain raw material specifications in accordance with compendial and internal requirements.
This role will provide critical support to accelerate regulatory commitments while enabling Material Sciences personnel to remain focused on strategic product and manufacturing priorities. The position will support specification updates, technical data gathering, compendial comparisons, document management, change control execution, and cross-functional implementation activities.
Key Responsibilities
Specification Remediation
• Review existing raw material specifications against current compendial requirements.
• Compare USP, Ph. Eur., JP, Client, and supplier specifications where applicable.
• Support revision of excipient, chemical, and process material specifications.
• Compile technical justification packages and supporting rationale for specification updates, where appropriate.
Change Control & CAPA Support
• Support initiation and execution of change controls related to specification updates.
• Coordinate impact assessments from affected functional groups.
• Track implementation progress and CAPA milestones.
• Assist with closure documentation and inspection readiness activities.
Data Management & Documentation
• Maintain specification inventories and implementation trackers.
• Generate summary reports and status dashboards.
• Verify technical data consistency across specifications and supporting documents.
• Ensure document formatting aligns with approved specification templates.
Cross-Functional Coordination
• Work with Material Sciences, Quality Systems, Quality Control, Regulatory Affairs, Supply Chain, Manufacturing, and Procurement.
• Follow up with SMEs regarding impact assessments and outstanding actions.
• Support meeting preparation and action item tracking.
Inspection Readiness
• Assemble supporting documentation for regulatory inspections and CAPA effectiveness reviews.
• Support ongoing alignment of specifications with compendial and regulatory expectations.
Required Qualifications
• BS degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related discipline.
• 3–4 years of experience in pharmaceutical manufacturing, quality, technical services, material sciences, or regulatory compliance.
• Experience working with GMP documentation.
• Strong technical writing and document revision skills.
• Familiarity with change controls, CAPAs, and deviation systems.
• Knowledge of pharmacopeial standards (USP, EP, JP).
Preferred Qualifications
• Experience with raw material specifications and supplier quality systems.
• Understanding of excipient and chemical control strategies.
• Experience supporting regulatory inspections or remediation programs.
• Familiarity with Veeva, document management systems, and electronic quality systems.
• Ability to independently manage multiple workstreams and priorities.
Success Metrics
• Specification revisions completed on schedule.
• Change control support delivered to meet CAPA milestones.
• Impact assessments and implementation activities tracked to completion.
• Inspection-ready documentation maintained.
BioMarin is seeking a temporary contractor to support execution of a global material specification remediation program associated with regulatory commitments and CAPA activities. The contractor will work closely with Material Sciences, Global Quality, Regulatory Compliance, and Site Quality teams to review, revise, implement, and maintain raw material specifications in accordance with compendial and internal requirements.
This role will provide critical support to accelerate regulatory commitments while enabling Material Sciences personnel to remain focused on strategic product and manufacturing priorities. The position will support specification updates, technical data gathering, compendial comparisons, document management, change control execution, and cross-functional implementation activities.
Key Responsibilities
Specification Remediation
• Review existing raw material specifications against current compendial requirements.
• Compare USP, Ph. Eur., JP, Client, and supplier specifications where applicable.
• Support revision of excipient, chemical, and process material specifications.
• Compile technical justification packages and supporting rationale for specification updates, where appropriate.
Change Control & CAPA Support
• Support initiation and execution of change controls related to specification updates.
• Coordinate impact assessments from affected functional groups.
• Track implementation progress and CAPA milestones.
• Assist with closure documentation and inspection readiness activities.
Data Management & Documentation
• Maintain specification inventories and implementation trackers.
• Generate summary reports and status dashboards.
• Verify technical data consistency across specifications and supporting documents.
• Ensure document formatting aligns with approved specification templates.
Cross-Functional Coordination
• Work with Material Sciences, Quality Systems, Quality Control, Regulatory Affairs, Supply Chain, Manufacturing, and Procurement.
• Follow up with SMEs regarding impact assessments and outstanding actions.
• Support meeting preparation and action item tracking.
Inspection Readiness
• Assemble supporting documentation for regulatory inspections and CAPA effectiveness reviews.
• Support ongoing alignment of specifications with compendial and regulatory expectations.
Required Qualifications
• BS degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related discipline.
• 3–4 years of experience in pharmaceutical manufacturing, quality, technical services, material sciences, or regulatory compliance.
• Experience working with GMP documentation.
• Strong technical writing and document revision skills.
• Familiarity with change controls, CAPAs, and deviation systems.
• Knowledge of pharmacopeial standards (USP, EP, JP).
Preferred Qualifications
• Experience with raw material specifications and supplier quality systems.
• Understanding of excipient and chemical control strategies.
• Experience supporting regulatory inspections or remediation programs.
• Familiarity with Veeva, document management systems, and electronic quality systems.
• Ability to independently manage multiple workstreams and priorities.
Success Metrics
• Specification revisions completed on schedule.
• Change control support delivered to meet CAPA milestones.
• Impact assessments and implementation activities tracked to completion.
• Inspection-ready documentation maintained.