(CW) Manufacturing Associate (Temporary/Contract)

BioMarin Pharmaceutical Inc
  • Novato, CA
    30+ days ago

    Job Description

    b' (CW) Manufacturing Associate (Temporary/Contract) | BioMarin Corporate \t \t \t \t \t \t \t \t \t \t \t \t \t \t \t \t

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    Novato

    BioMarin Pharmaceutical

    (CW) Manufacturing Associate (Temporary/Contract)

    Location: Novato, United States

    Workstyle: Onsite Only

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    Who We Are

    BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.

    Guided by our purpose to develop medicines that make a profound impact on peopleâ€s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.

    Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.

    CONTRACT ROLE SHIFT Schedule: The schedule will be from 6:00 pm to 7:00 am, with the first week covering Wednesday to Saturday, and the following week rotating to Wednesday to Friday. This means the schedule alternates each week between four and three nights.

    Duties

    PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.).

    TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents.

    QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).

    BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics.

    WORK ENVIRONMENT/PHYSICAL DEMANDS

    • Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.

    • Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.

    • May require work around loud equipment. • The use of personal protective equipment will be required.

    • Requires various shift based work and off hours.

    Skills

    • Strong communication skillsâ€"verbal and written

    • Ability to work in a team environment which includes good conflict resolution and collaboration

    • Displays good initiative to identify areas for improvement and implement solutions

    Education

    • Bachelorâ€s degree in science related area or engineering
    • Associateâ€s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry Reason for Request: Comments for Suppliers:

    BioMarinâ€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 BioMarinâ€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.

    PASTE JOB POSTING TEXT HERE

    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.

    Apply

    Recruitment Fraud Alert Notice

    Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent BioMarin in recruitment activities. We have an established recruitment process which is required for all posted positions by BioMarin prior to issuing an offer of employment. This BioMarin process requires formal interviews conducted live with personnel representing BioMarin and never requires payments or fees from job applicants. BioMarin does not conduct interviews via texting tools such as RingCentral.

    In the event you receive a suspicious email message about recruiting on behalf of BioMarin, unless it's from a BioMarin authorized recruiting partner, do not provide any personal information or pay any fees. Qualified and interested candidates should apply to current openings directly through this BioMarin website. BioMarin accepts no responsibility for any costs or charges incurred as a result of fraudulent activity.

    If you have lost money or provided your personal identifying information, please contact your bank and report the matter to the FBI via www.ic3.gov. We would also suggest you notify your local police department and monitor your credit.

    For more information on how to recognize and report phishing scams visit: https://consumer.ftc.gov/articles/how-recognize-and-avoid-phishing-scams or https://consumer.ftc.gov/consumer-alerts/2023/01/looking-job-scammers-might-be-looking-you

    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.

    If you have a disability and believe you need a reasonable accommodation in order to search for a job opening or apply for a position, email Applicant_accommodations@bmrn.com with your request.

    This email address is not for general employment inquiries or correspondence. We will only respond to those requests that are related to the accessibility of the online application system due to a disability.

    BioMarin Pharmaceutical does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. We handle all recruiting through our Talent Acquisition team â€" please do not contact hiring managers directly. Agencies who wish to offer their services to BioMarin Pharmaceutical may contact us at talentacquisition@bmrn.com.

    Applicants, please do not use this email address to submit resumes â€" if you do so, you will be redirected to apply through the website.

    Click here to review "EEO Is The Law" poster. Click here to review the Pay Transparency Nondiscrimination Statement. Click here to review the Notification of Employee Rights under Federal Labor Laws.

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    Numbers & Facts

    LocationNovato, CA

    Skills

    • Adverse Eventsunmatched
    • Biotech and Pharmaceuticalunmatched
    • Business Skillsunmatched
    • Business Solutionsunmatched
    • Business Supportunmatched
    • Cell Culturesunmatched
    • Change Requests/Ordersunmatched
    • Clinical Trialunmatched
    • Column Chromatographyunmatched
    • Communication Skillsunmatched
    • Conflict Resolutionunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Diseaseunmatched
    • ERP (Enterprise Resource Planning)unmatched
    • Facebookunmatched
    • Geneticsunmatched
    • LinkedInunmatched
    • Manufacturingunmatched
    • Manufacturing/Industrial Processesunmatched
    • Medical Productsunmatched
    • Medical Recordsunmatched
    • Medicineunmatched
    • Metricsunmatched
    • Needs Assessmentunmatched
    • Operations Processesunmatched
    • Physical Demandsunmatched
    • Process Improvementunmatched
    • Protein Purificationunmatched
    • Publicationsunmatched
    • Quality Assuranceunmatched
    • Quality Controlunmatched
    • RADIUS (Remote Authentication Dial-In User Service)unmatched
    • Regulationsunmatched
    • Supply Chainunmatched
    • Team Playerunmatched
    • Technical Operationsunmatched
    • Technical Writingunmatched

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