About this opportunity

Who We Are BioMarin is a leading, global rare disease biotechnology company focused on delivering medicines for people living with genetically defined conditions. Founded in 1997, the San Rafael, California-based company has a proven track record of innovation, with multiple commercial therapies and a strong clinical and preclinical pipeline. Using a distinctive approach to drug discovery and development, BioMarin seeks to unleash the full potential of genetic science by pursuing category-defining medicines that have a profound impact on patients.. About Technical Operations 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 Shanbally, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution.GEO Operations ManagerAs part of BioMarin’s TOPS group, Global External Operation (GEO) has responsibility for managing all external manufacturing operations and performance at Contract Manufacturing Organizations (CMOs).The GEO Operations Manager is responsible for managing day-to-day activities at one or more CMOs. Operations may include drug product operations (biologics and/or small molecules) and/or finished-goods packaging. Both clinical and commercial activities are in scope for each area, as requiredThe role also supports operational readiness for new CMOs or new processing steps at an existing CMO. The successful candidate will partner with SMEs (both internally and with externally), as needed, to ensure quality product is delivered on time and in full.Key Responsibilities:<ul><li>Execute with the CMO the production plan to deliver an uninterrupted supply of clinical & commercial product</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Manage the CMO meeting schedule in conjunction with your cross functional colleagues to ensure an engaging and collaborative environment.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Identify any supply constraints and negotiate/resolve with the CMO any issues to meet the supply plan.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Manage escalations and communications within the process team/GEO site from an operations perspective. </li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Collaborate with a cross functional team to ensure uninterrupted supply of product. This will involve both process team and non-process team colleagues.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Perform root cause analysis or equivalent to understand issues and implement corrective actions as appropriate.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Manage material movement between CMO sites with various internal partners.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Attend at CMO to monitor production campaigns and develop an in-depth knowledge of the manufacturing process and systems at the CMO.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Manage and maintain with cross functional team a visual metric/dashboard to provide an oversight of the GEO business.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Coordinate as required BioMarin activities in the evaluation of process changes, change requests and deviations to ensure timely resolution without impacting on supply.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Act as the focus and conduit for communications between the CMO and with members of BioMarin manufacturing group and other departments to meet the supply plan.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Lead and/or participate in technology transfers, new product launches, validation activities with the CMO and internal cross functional teams including Process Development, Regulatory Affairs and Quality departments </li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Contribute to the development of formal systems and procedures for the selection of CMO</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Initiate and implement necessary control systems within budget and to reduce cost of goods</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">With the Corporate Compliance and Quality departments, ensure that the CMO is compliant with cGMPs.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Support contracts and negotiations with CMO in collaboration with the procurement and EPM teams.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Represent assigned product, CMO and GEO Ops team at appropriate meetings, e.g. VPT, VST.</li></ul><div style="line-height: 112.0%;"> Additional ORP focused responsibilities, (as required): </div><ul style="margin-top: 0.0px;"><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Establish and maintain GEO’s processes and project templates for ORP management. </li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Carry out Operations Gap Analysis of new CMOs and establish and lead subsequent mitigation plans. </li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Ensure smooth transition of Operations activities from PPQ/Launch Phase into the Commercial Process Team.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Lead site exit projects as required for GEO. </li></ul><div style="line-height: 112.0%;"> </div><div>EXPERIENCE & Skills:</div><div style="margin-bottom: 8.0pt;line-height: 112.0%;">Minimum requirement of 5 years leadership experience in Operations, Supply Chain or Quality.</div><ul style="margin-top: 0.0px;"><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">BS/BA degree; life sciences, business, or supply chain management </li></ul><div style="line-height: 112.0%;">Required skills needed to accomplish the responsibilities/essential functions include:</div><div style="line-height: 112.0%;"></div><ul style="margin-top: 0.0px;"><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Will have an excellent understanding of the processes/unit operations.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Demonstrated ability in leading/managing cross functional, multi-disciplinary teams.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Ability to guide and support cross functional teams in the resolution of short-term issues and sustained performance for long-term goals.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Proven track records in effective decision making.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">A high level of initiative, influencing, coaching as well as excellent organizational skills.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Experienced in working and managing in a regulated GXP environment.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Strong stakeholder and relationship management experience.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Experience with CAPA, FMEA, RCA tools in a highly regulated manufacturing environment is desired.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Excellent organizational, written and verbal communication, commercial acumen.</li><li style="font-family: sans-serif , arial , helvetica;font-size: 11.0pt;">Experience in supply planning or inventory management.</li></ul> 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.

Job details

Seniority

Manager

Function

Manufacturing & CMC

Therapeutic area

Not listed

Location

United States

Employment type

Fulltime-Regular

How this role compares

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

We currently track 452 comparable Manager Manufacturing & CMC roles across 73 biopharma companies.

452Comparable roles tracked

433Currently active

73Companies hiring similar roles

31Countries represented

Salary context

141 of 452 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting

Lowest disclosed · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)

Highest disclosed · Regional Manager - Megasys · Merck KGaA $220,000/yr – $250,000/yr

Peer group range $0 – $235,000 (median $157,000)

Where these roles are based

Top locations among the 452 comparable roles

United States272

India55

Netherlands16

Ireland16

United Kingdom11

Japan10

+ 25 more countries

Seniority mix

452 of 452 peers have a known seniority level

Manager247

Associate131

Associate Director74

Therapeutic area mix

3 of 452 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease2

Vaccines & Infectious Disease1

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.

Merck West Point, Pennsylvania, United States of America Manager