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Lead, Manufacturing (Day Shift)

BioMarin Pharmaceutical Inc.

Novato (CA)

On-site

USD 68,000 - 103,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a Manufacturing Shift Lead to oversee daily operations in a cutting-edge biotechnology environment. This role involves leading a team, ensuring compliance with regulatory standards, and managing production schedules. The ideal candidate will have a solid background in manufacturing processes and team leadership, with a focus on continuous improvement. Join a company dedicated to advancing human health through innovative science and contribute to the development of transformative medicines. This is an exciting opportunity to make a significant impact in the biotechnology field while working in a collaborative and dynamic setting.

Benefits

Medical Benefits
Discretionary Bonus
Long-term Incentive Units

Qualifications

  • 2-4 years of manufacturing experience with a focus on team leadership.
  • Familiarity with manufacturing software and equipment.

Responsibilities

  • Lead daily operations with effective communication and decision-making.
  • Provide training and direction to staff while ensuring compliance.

Skills

Manufacturing Experience
Team Leadership
Problem Solving
Communication Skills

Education

BA/BS in relevant field

Tools

Oracle
MES
Manufacturing Software
Chrome Skids
TFF Skids

Job description

About Technical Operations

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.


Manufacturing Shift Lead


Summary
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These individuals build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.


Responsibilities

  1. Leadership
  2. Accountable for the daily operations in area, requiring effective communication to make appropriate decisions, trouble shooting, and schedule adherences with minimal oversight
  3. Accomplishes tasks through direct and effective coordination
  4. Provides direction and hands-on training for staff
  5. Supports the management of staff with supervisor
  6. Lives department values and sets the standards for others to operate
  7. Fosters an environment of compliance, strong work ethic and ongoing learning
  8. Contribution
  9. Ability to take responsibility for moderate level projects
  10. Effective interaction with peer Leads across manufacturing to create alignment and improvement
  11. Partners with support groups (Facilities, Validation, Quality) to complete scheduled activities
  12. Process Knowledge
  13. Strong knowledge and experience in all aspects of relevant process theory, equipment, and compliance
  14. Ability to troubleshoot, identify issues and support resolutions with technical groups
  15. Required to perform ongoing operational tasks in respective work area
  16. Uses scientific thinking and decision making in daily work
  17. Technical Competency
  18. Proven experience with relevant process, theory and equipment
  19. Experience with process automation and functionality
  20. Assist with review and approval of documentation including Batch Records and logbooks
  21. Support the closure of Manufacturing owned Quality Records (deviations, change requests)
  22. Other duties as assigned

Experience

Required Skills:
2-4 years Manufacturing Experience
0-2 years Leading a team
Familiarity with manufacturing softwares, Chrome skids, TFF skids
Delegating work, leading a team, following production schedule


Desired Skills:
2-4 years Manufacturing Experience
0-2 years Leading a team
Desired skills is experience with Oracle, MES, Microsoft Teams, communication with groups


EDUCATION
BA/BS Desired Not Required, 1-2 Years Leading Manufacturing Experience


EQUIPMENT
Chrome Skids, TFF skids, buffer tanks, labwashers, autoclaves


CONTACTS
Will interact with manufacturing, automation, facilities, instrumentation, QA, QC


SHIFT DETAILS
This position is for the Back half Day shift Wed/Thurs-Sat 6am-7pm


ONSITE, REMOTE, OR FLEXIBLE
Onsite only


Travel Required
None


Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.


Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.


Equal Opportunity Employer/Veterans/Disabled
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, or protected veteran status and will not be discriminated against on the basis of disability.


In the U.S., the salary range for this position is $ 68,300 to $ 102,500 per year, which factors in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. A discretionary bonus and/or long-term incentive units may be provided as part of the compensation package, in addition to the full range of medical, financial, and/or other benefits, dependent on the level and position offered.

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