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BioMarin Pharmaceutical Inc.

Sr. Project Manager 2

BioMarin Pharmaceutical Inc., Novato, California, United States, 94949


Who We Are

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.Sr Project Manager 2

SUMMARY

The role will act as a Project Manager within the

California Facilities and Engineering

group

in the Capital Project Delivery function

.

Assignment of projects will be limited to

CA

based projects.

RESPONSIBILITIES

Implement, and manage capital projects using

industry

best practices

and

BioMarin

business processes

.Manage the scope, deliverables, schedule, project team, and budget for capital expenditure (

CapEx

) projects.Participate in the development and evaluation of RFP and bidder/vendor analysis

for General contracting and engineering services

when design build

method

usedWorks directly with project controls to

p

repare and update project status, schedule

, resource,

and cost reports within Oracle based tools (OPPM & P6) for the use of numerous BMRN

departmentsIdentify Develop

and oversee internal

and external

project team(s) composed of various BMRN engineers, EHS&S, IT, manufacturing, maintenance,

and etc.

personnel.Ensure internal employees, consultants & contractors working on any construction related projects maintain compliance with all

GMP

requirements (including training)

,

EHS&S and security requirements, including completion and review of Job Hazard Assessments

and BioMarin policies.Evaluate, prepare, & submit

OPPM

project intake forms

once a pre-governance

screening has taken place and project will move forwa

rd

.Manage all governance

requirements utilizing the project lifecycle business process

and Capital Portfolio Management Guidelines.Works

with

project controls for

the generation of project cost accrual information, in service dates, financial long-range planning, & other financial and planning exercises.C

oordinate/support

engineering and automation design,

commissioning, qualification and

the

QA Validation groups

as app

ropriate.Proactively look for and recommend improvements in site processes and

procedures.Represent the

Capital Project Delivery group

with good communication and presentation skills.Provide monthly reporting on Projects to

Senior

Management as required.EXPERIENCE

Minimum 10

years of project management experience

preferably in the biotech or pharmac

eutical organizationPMP certificate highly desirable.Desired Skills:

Ability to work with

minimal direct

supervision: meet deadlines, prioritize assignments, provide recommendations and effectively communicate

updates.Experienced

with communicating with in supporting

Executive

Management as well as providing

direction support

for

multiple

projects

simultaneously.Must be very organized and possess strong verbal and written communications

skillsMust be proficient with Internet navigation, Microsoft Office (Outlook, Word, PowerPoint, Excel, Project, Teams,

Sharepoint

), Adobe AcrobatFamiliarity with Oracle Primavera P6Should be flexible to

working outside the core business hours (occasionally on short notice, and a limited basis) as

needed.Proven ability to manage multiple and fast-moving

priorities.Ability to work well in a fast-paced collaborative team environment within a rapidly evolving business

environment.Skilled at solving multi-dimensional problems with both quantitative and qualitative

variables.Ability to lead and influence others in support of company

objectives.Excellent decision making and cross functional team building skills.Solid understanding of GMP

, GLP

, and non-GMP

project requirementsAble to read and understand architectural and engineering plans and

specifications.Good understand of construction contract types,

delivery methods, and

construction management

processes.EDUCATION

BS degree from an accredited university in a construction or engineering related field.Could be a combination of AS degree and industry experience.EQUIPMENT

All equipment needed will be provided by

BioMarin.

CONTACTS

Project controlsProject Engineering both Automation and FUESite Engineering and AutomationCommiss

ioning and QualificationSite ValidationQuality ValidationAll User groups in business (TOPS, R&D,

Corporate)SHIFT DETAILS

Standard day shift

ONSITE, REMOTE

,

OR

FLEXIBLE

Flexible 3-5 days on site

or as needed to facilitate team meetings, contractor supervision and

site job walks.

TRAVEL REQUIRED

Travel less than 5%

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.

In the U.S., the salary range for this position is $ 128,000 to $ 192,000 per year, which factors in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. A discretionary bonus and/or long-term incentive units may be provided as part of the compensation package, in addition to the full range of medical, financial, and/or other benefits, dependent on the level and position offered.#J-18808-Ljbffr