Sr. Supervisor, Manufacturing (Day Shift)

Bimbo Bakeries USA, Inc.; Novato (CA); On-site; USD 95,000 - 131,000; Full time

Job summary

A leading biotechnology company seeks a manufacturing leader in their Technical Operations group. The role involves overseeing daily operations, staff training, and compliance in a high-quality production environment. With transformation at its core, this position offers the chance to make a significant impact in drug development.

Benefits

Medical insurance

Dental and vision insurance

Life insurance

Paid time off

Discretionary stock-based incentives

Qualifications

• 4-6 years of manufacturing experience.
• 2+ years leading a manufacturing team.
• Familiarity with manufacturing software and regulations.

Responsibilities

• Accountable for daily operations with minimal oversight.
• Provides direction and training for staff.
• Supports compliance and operational tasks with scientific decision-making.

Skills

Manufacturing Experience

Team Leadership

Technical Decision Making

Communication Skills

Troubleshooting

Process Knowledge

Education

BA/BS degree (desired)

Tools

Manufacturing Software

Oracle

MES

Job description

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.

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

• Leadership

• Accountable for the daily operations in area, requiring effective communication to make appropriate decisions, trouble shooting, and schedule adherences with minimal oversight

• Accomplishes tasks through direct and effective coordination

• Provides direction and hands-on training for staff

• Supports the management of staffwith supervisor

• Lives department values and sets the standards for others to operate

• Fosters an environment of compliance, strong work ethic and ongoing learning

• Contribution

• Ability to take responsibility for moderate level projects

• Effective interaction with peer Leads across manufacturing to create alignment and improvement

• Partners with support groups (Facilities, Validation, Quality) to complete scheduled activities

• Process Knowledge

• Strong knowledge and experience in all aspects of relevant process theory, equipment, and compliance

• Ability to troubleshoot, identify issues and support resolutions with technical groups

• Required to perform ongoing operational tasks in respective work area

• Uses scientific thinking and decision making in daily work

• Technical Competency

• Proven experience with relevant process, theory and equipment

• Experience with process automation and functionality

• Assist with review and approval of documentation including Batch Records and logbooks

o Support the closure of Manufacturing owned Quality Records (deviations, change requests)

EXPERIENCE

Required Skills:

4-6 years Manufacturing Experience 2+ years Leading a team

Familiarity with manufacturing software, Chrome skids, TFF skids

Delegating work, leading a team, following production schedule

Desired Skills:

4-6 years Manufacturing Experience 2+ years Leading a team

Experience with Oracle, MES, Microsoft Teams, strong communication skills

EDUCATION

BA/BS desired not required

EQUIPMENT

Chromatography Skids, TFF skids, buffer tanks, Labwashers, Autoclaves

CONTACTS

Will interact with Manufacturing, Automation, Facilities, Instrumentation, QA, QC, Validation

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

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.
The salary range for this position is: $95,000 to $130,680. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

For additional benefits information, visit: https://careers.biomarin.com/benefits .

• Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.