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 DESCRIPTION

The overall Supply Chain Operations (SCO) department is responsible for the site planning & scheduling, Raw Materials Purchasing, Oracle recipe management, VMI (Vendor Managed Inventory), Materials management, Warehouse, Dispensing/Sampling and Shipping to customers.
Reporting to the Supply Chain Operations Manager of the functional area, the primary role of the SCO BPS & PIR Lead is to provide SCO technical leadership and lead permanent inspection readiness within SCO. The lead will be committed to team development, continuous improvement and compliance. A high level of initiative, influencing and questioning skills are key role requirements, as well as excellent organisational skills.

SKILLS

• Demonstrated experience working with MFG processes, device assembly and secondary packaging operations in a cGMP environment
• Past experience and demonstrated ability to successfully influence team performance in a high performance team is preferred
• Demonstrate strong communication skills and the ability to interact across cross-functional teams
• Track record of embedding a strong Quality and Safety culture
• Strong process knowledge of quality systems
• Excellent project management skills
• Proven ability to lead and deliver on multiple and agile and flexible to work on multiple initiatives
• Strong continuous improvement focus
• Strong collaboration skills
• Experience with site regulatory inspections and direct interaction with regulatory inspectors
• Highly developed organizational and leadership skills

EDUCATION

• Bachelor degree in biotechnology, chemical or biochemical engineering, biochemistry or bio-systems engineering or related field or equivalent experience in a GMP environment is preferred.
• Other continuing education initiatives highly desirable (e.g. Six Sigma, Lean Manufacturing, industry specific coursework).

EXPERIENCE

• At least 3 years experience in a regulated manufacturing environment with excellent knowledge of quality systems.
• Demonstrated ability to partner with other functional groups to achieve business objectives.
• Strong knowledge of cGMPs (US & EU), OSHA, ISO, and other regulatory agency standards and requirements applicable to material operations in a pharmaceutical production facility.
• Strong communication and interpersonal skills – oral, written and formal presentation skills.
• Creative problem solving skills.
  We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.
  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