About this opportunity

<div>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. Our manufacturing and process development teams manage the production of our therapies for clinical trials and commercial markets. These engineers, technicians, scientists, and support professionals continually provide quality assurance and ensure we meet all regulatory standards. We have manufacturing facilities in Northern California and in Cork, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution. 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.</div><div> </div><div style="text-align: center;">Title: Material Planner</div><div style="text-align: center;">Work Type: Contract </div><div style="text-align: center;">Duration: 12 Months </div><div> </div><div>Role</div><div>The primary role of the Material Planner is to ensure the availability of raw material components to meet the production schedule in Drug Substance, Drug Product and Finish Goods Packaging Operations. Ensure raw material components are planned, purchased and released within the guidelines established in the ERP SAP system. The Material Planner will play a key role in the development and implementation of systems and processes to ensure optimal raw material coverage in line with the Master Production Schedule as well as product launch activities. </div><div> </div><div>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.</div><div> </div><div>Key Responsiblities: </div><ul style="margin-top: 0.0cm;"><li style="">Responsible for Material Requirements Planning (MRP) in line with the Master Production Schedule in SAP to ensure that operational requirements are met</li><li style="">Responsible for converting purchase requestions to purchase order as required by SAP detail schedule including payment of supplier invoices</li><li style="">Responsible for monitoring Materials release status to meet detailed schedule</li><li style="">Responsible for Inventory Management end to end including (Pricing (Purchase Info Record), Purchase Price Variance (PPV), reserve process, expiry, FIFO, FEFO, safety stock, lead times etc)</li><li style="">Responsible for issuing quarterly supplier forecasts</li><li style="">Responsible for generating and issuing recurring Heatmap/Material Readiness to site stakeholders. Participate in weekly material readiness activity.</li><li style="">Responsible for ensuring that supplier open order book is issued and aligned with SAP on a weekly basis.</li><li style="">Responsible for Master Data accuracy in SAP for material components</li><li style="">Responsible for aging receipts, resolving issues and identifying root causes</li><li style="">Responsible for Short Term Exception Management (STEM) program as required and proactively engage with stakeholders to resolve schedule conflicts.</li><li style="">Responsible for inputs into the monthly site Supply Chain Review meeting (SCR)</li><li style="">Participate in end of campaign performance review (Plan V Actual) to correct future campaign requirements </li><li style="">Participate in Global Category Form and Quarterly Business Review (QBR)</li><li style="">Participate in site Single Use Application strategy meetings</li><li style="">Member of the functional process team level as required</li><li style="">Facilitate Tier 1 Purchasing team meeting</li><li style="">Complete material planning scenarios as required to maintain detailed schedule </li><li style="">e as required in delivery of Change Request, CAPA ,Deviation & Supplier Change Notification (SCN) within the Quality Management System (QMS) system </li><li style="">Engage Right First Time (six-sigma) and lean manufacturing practices leading to Operational Excellence</li><li style="">Develop, maintain and publish KPI’s for supplier performance (OTIF)</li><li style="">Participate in Continuous Improvement (CI) projects </li><ul style="margin-top: 0.0cm;"><li style="">Safety and Quality </li><li style="">Standard Operating Procedures (SOP) </li></ul><li style="">Participate in daily cross-functional meetings to ensure maintenance of Adherence to Schedule *(ATS) and Adherence to Plan *(ATP) in line with Make / Assess / Release commitments </li><li style="">Participate in weekly S&OE meetings ensuring cross functional alignment of plans </li><ul style="margin-top: 0.0cm;"><li style="">Participate in Material Planner Standard Work</li><li style="">Metrics</li><li style="">Cost Savings </li><li style="">Dual Sourcing </li><li style="">Operational Readiness Programs (ORP)</li></ul><li style="">List above identify key responsibility, but other duties maybe required as per business needs </li></ul><div>Knowledge, Skills and Capabilities </div><ul style="margin-top: 0.0cm;"><li style="">Development of efficient and effective Material planning processes and systems</li><li style="">Engage with vendors in an ethical and compliant manner when required</li><li style="">Be “Patient & Customer focused” ensuring that requirements are clearly planned for and communicated within the organization</li><li style="">Be Results driven, while ensuring the optimization and efficient use of cross functional resources</li><li style="">Contribute to the innovation and continuous improvement (CI) within Material Operations and BioMarin</li><li style="">Be collaborative and cross-functional with all other departments within the site and across the wider BioMarin community</li><li style="">Ensure department and personal “goals and objectives” are completed in an effective and efficient manner</li><li style="">A strong strategic thinker who can perform at both a strategic and tactical level when and where required within and across the organization</li><li style="">Ensure a high level of integrity always while performing the role</li><li style="">Demonstrate the drive and eagerness to be successful in this role with a view to developing and progressing to levels of increasing responsibility.</li><li style="">Education & Experience</li><li style="">A minimum of an Honor's Degree (NFQ level 7) in Supply Chain Management or other related Business discipline is essential</li><li style="">Supply Chain Certification is preferred e.g. APICS</li><li style="">Project Management or Lean Certification is desirable</li></ul><div>Experience </div><ul style="margin-top: 0.0cm;"><li style="">A minimum of 2 years relevant Supply Chain Management experience</li><li style="">Experience in Planning/Purchasing in a pharmaceutical environment with strong technical/systems background is desirable</li><li style="">Experience of SAP is essential </li><li style="">Prove track record in end to end leading and managing of a direct material category (specific experience managing chemicals, SUT's (Single Use Technologies) highly desirable</li><li style="">Power BI or similar data analytics visual tool knowledge is desirable but not essential</li><li style="">Experience working in a GMP environment for a minimum of 1 years</li><li style="">Project Management with a focus on value creation and waste reduction programmes highly desirable</li></ul><div style="margin-left: 18.0pt;"> 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.</div><div> </div>

Job details

Seniority

Not listed

Function

Manufacturing & CMC

Therapeutic area

Not listed

Location

Cork, Ireland

Employment type

Fulltime-Temporary

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 2402 comparable Manufacturing & CMC roles across 163 biopharma companies.

2402Comparable roles tracked

2290Currently active

163Companies hiring similar roles

52Countries represented

Salary context

652 of 2402 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting

Lowest disclosed · Supervisor, Manufacturing Operations (Second Shift) · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)

Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr

Peer group range $0 – $314,750 (median $123,850)

Where these roles are based

Top locations among the 2402 comparable roles

United States1163

India150

Germany117

France91

Netherlands89

Ireland84

+ 46 more countries

Seniority mix

1099 of 2402 peers have a known seniority level

Senior324

Manager248

Associate131

Intern/Fellow/Postdoc110

Principal92

Director82

Associate Director74

Senior Director31

Executive/VP7

Therapeutic area mix

12 of 2402 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease9

Rare Disease2

Oncology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar

Director, Combination Product Development

McDermott Laboratories Limited Northern Cross, Ireland Director

Same function Same country

40%similar

Maintenance Technician

Mylan Teoranta Inverin, Ireland

Same function Same country

40%similar

Cleaning Validation Specialist

Mylan Teoranta Inverin, Ireland

Same function Same country

40%similar

Senior Process Engineer

Mylan Teoranta Inverin, Ireland Senior

Same function Same country

40%similar

Head of External Sterile Operations (Anywhere in Europe)

Viatris Healthcare Northern Cross, Ireland

Same function Same country

40%similar

Planning Master Data Analyst (12 month FTC)

McDermott Laboratories Limited Northern Cross, Ireland

Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%

Director, Combination Product Development

McDermott Laboratories Limited · Northern Cross, Ireland · Director

Function Therapeutic area Seniority Country

40%

Senior Process Engineer

Mylan Teoranta · Inverin, Ireland · Senior

Function Therapeutic area Seniority Country

40%

Director of Engineering

Mylan Teoranta · Inverin, Ireland · Director

Function Therapeutic area Seniority Country

40%

Senior Project Engineer

Regeneron Ireland · Limerick, Ireland · Senior

Function Therapeutic area Seniority Country

Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.