Manager, Downstream Operations

at  Thermo Fisher Scientific

Carlsbad, CA 92008, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate07 Feb, 2025USD 154700 Annual08 Nov, 20242 year(s) or aboveLeadership Skills,Documentation,Progression,Excel,Process Engineering,Addition,Equipment Maintenance,Manufacturing,Microsoft Word,Outlook,FinanceNoNo
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Description:

EDUCATION

  • Bachelor’s degree required, advanced degree such as an MBA is a plus.

EXPERIENCE

  • 3+ years of progression in manufacturing leadership roles of growing responsibility, with a preference for experience in reagent consumables manufacturing settings requiring high reliance on effective equipment maintenance and capital planning.
  • 2+ years of experience in ISO or cGMP-regulated manufacturing environment.
  • Solid ERP system knowledge and an understanding of cost accounting/standard manufacturing financials.

KNOWLEDGE, SKILLS, ABILITIES

  • Must demonstrate strong leadership abilities with capability to use diverse resources, respond quickly, understand impact of changes and decisions, facilitate agreement, build collaborative relationships and understand customer needs
  • Knowledge of process engineering, standardization and documentation and strong organizational and leadership skills, with proven track record to successfully plan, implement and coordinate programs to achieve business objectives.
  • Possesses a continuous process improvement approach with the ability to effectively lead and manage change.
  • Is energized working in a fast-paced environment.
  • Consistent, diligent and accurate in carrying out responsibilities.
  • Is curious, inquisitive, innovative, never satisfied with the status quo.
  • Possesses a solid working knowledge of other business functions such as Logistics, Finance, Engineering, Planning, EH&S, facilities, in addition to Manufacturing and Quality.
  • Proficient in PC applications, including Microsoft Word, Excel, and Outlook.
    This position does not offer relocation benefits.

Responsibilities:

  • Promotes and facilitates the safest working environment for all employees and ensures all team members work safely with equipment, chemicals, and hazardous materials.
  • Follows all ISO & Regulatory Compliance standards.
  • Effectively leads manufacturing scientists and other people leaders to produce high quality reagent buffers, protein formulations, and electrophoresis gels.
  • Ensures proper staffing and training for each manufacturing team to meet compliance requirements and customer demand efficiently.
  • Drives Practical Process Improvements (PPI) with a high level of team member involvement and engagement.
  • Supports career development plans and performs team performance evaluations.
  • Effectively communicates barriers or issues and obtains needed support for resolution.
  • Accountable for ensuring system data integrity for manufacturing data elements (BOM, Routing, ACQ, Lead Times).
  • Handles expenses to meet budgets and financial objectives and proactively seeks opportunities to drive improvement of the operating results.
  • Works with team members and planning/purchasing teams to develop and implement a manufacturing schedule to meet customer demands.
  • Participates in internal and external audits, responds to audit observations, and identifies and implements appropriate corrective and preventive actions.
  • Acts as a liaison with Product Managers/Business Leaders and members of other operations departments and sites.
  • Performs other duties and cross-training as assigned


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

MBA

Proficient

1

Carlsbad, CA 92008, USA