Director of Manufacturing Science

Grifols Shared Services North America, Inc

San Diego (CA)

On-site

USD 199,000 - 270,000

Full time

14 days+
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Benefits offered by this job

Medical
Dental
Vision
PTO
401(K) match
Tuition reimbursement

Job summary

Grifols is seeking a Director of Manufacturing Science in California to lead the MS department, guiding process improvements, tech transfer, and lifecycle management for blood screening products.

The role oversees Oligonucleotide Development, Product Support, Pilot Plant, Tech Writing, and Product Engineering, while ensuring GMP compliance, budget adherence, and staff development.

Qualifications

  • Advanced degree in biochemical/chemical engineering or related field.
  • 15+ years industrial experience with required degree.
  • Minimum 8 years supervisory experience.
  • Experience leading cross-functional manufacturing projects and tech transfers.

Responsibilities

  • Develops MS strategies and roadmap for process/equipment improvements.
  • Leads tech transfer from R&D to full-scale manufacturing.
  • Oversees NCR investigations and cleaning validation inputs.
  • Manages budgets and cross-functional project initiatives.
  • Coaches staff and drives continuous improvement.

Skills

Leadership
Communication
Project management
Lean Manufacturing
GMP knowledge

Education

Biochemical Eng (BSc/MSc/PhD)

Tools

MS Office

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Summary

Provides strategic and tactical leadership for the Manufacturing Support Department and is accountable for providing technical input and support for the manufacture of existing blood screening products, receiving and implementing tech transfer for major process changes and new products, troubleshooting manufacturing issues and making improvements to the existing manufacturing processes. Manages functional areas of Oligonucleotide Development, Product Support, Pilot Plant, Tech Writing, and Product Engineering functions.

Position Responsibilities
  • Develops MS strategies and roadmap for implementing process/equipment improvements and troubleshooting existing process issues.
  • Is the SME for the overlap of process, equipment, manufacturing technique and underlying science in the products we manufacture
  • Provides technical and scientific input into cleaning and process validations, NCR investigations and ongoing training of manufacturing personnel.
  • Leads the tech transfer from R&D and successful implementation into full-scale manufacturing production, include process development, when required
  • Leads the engineering and full scale investigation runs required for NCR investigations, process / equipment changes.
  • Provides guidance in evaluating process improvements and/or modifications between existing Manufacturing operations and key project teams.
  • Responsible for both internal and external manufacturing project initiatives
  • Ensures projects are implemented successfully, on time and within budget.
  • Provides on-going coaching to staff and measures team effectiveness
  • Drives continuous improvement and other projects (functional and cross-functional) as needed
  • Collaborates with the Team in lowering the cost of goods for manufactured products, maintains cost center and project budgets
  • Proficient MS Office (word, powerpoint, Excel)
Key Performance Indicators
  • Timely NCR and CAPA closures
  • Ensure projects are completed per project milestones
  • Ensures proper evaluation of impacts or any process related changes.
  • Ensures that processes are in a state of control (KPI trends)
  • Ensures that major manufacturing processes have a robust life-cycle management program (including emphasis on process robustness and economics) in place
  • Ensures that there exists a suitable balance between the resourcing for commercial manufacturing support, technology transfers and process stewardship in line with Grifols Divisional expectations
  • Successful technology transfers and technical manufacturing support of the site
  • Adherence to agreed financial budgets and cost of goods targets
  • Yield and reject targets met
Education

B.Sc., M.Sc. or Ph.D. in Biochemical or Chemical Engineering, Biology or related discipline

Experience
  • ≥15 years of industrial experience with B.Sc/M.Sc. or ≥10 years of experience with Ph.D. in Biochemical or Chemical Engineering, Biology or related discipline
  • Minimum of 8 years supervisory experience
  • Extensive experience working on multiple overlapping projects with complex interactions and a track record of completing projects on time and successfully.
  • Must have previously led a successful department of technical staff.
  • Knowledge of cGMP environments and Lifecycle process and cleaning validation requirements
  • Excellent communication skills, especially technical writing and presentations
  • Excellent skills in leading discussions of data with peers such as scientists and functional area managers
  • Excellent time management and project management skills
  • Expetise in building highly effective teams
  • Proven success as a leader in a collaborative manufacturing environment
  • Builds strong working relationships with cross-functional stakeholders and co-workers
  • Previous experience supporting FDS and other Regulatory inspections
  • 5S, OpEx and Lean Manufacturing experience a plus
  • Exceptional people management skills

The estimated pay scale for Director, Manufacturing Science role based in California, is $199,000.00 - $270,000.00 per year. Additionally, the position is eligible to participate in up to 30% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!

  • Medical
  • Dental
  • Vision
  • life insurance
  • PTO
  • paid holidays
  • up to 5% 401(K) match
  • tuition reimbursement

Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.

Location: NORTH AMERICA : USA : CA-San Diego:USSDW - San Diego CA - Willow Ct Mfg

Learn more about Grifols (https://www.grifols.com/en/what-we-do)

Type: Regular Full-Time

Job Category: MANUFACTURING

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