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Production/Manufacturing Planner (cGMP – Pharmaceutical) JD819745

JD819745

DPS is looking for a proven Production Planner to work with a pharmaceutical client in the Boston, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. Previous CMO knowledge is also strongly preferred.

Category:
Engineer Planning / Coordination
Location:
Massachusetts
Years of Experience Req.:
5+
Date Posted:
15/08/2019
Days Remaining:
9
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

Production/Manufacturing Planner (cGMP – Pharmaceutical)               JD819745

Boston, MA

 

Summary:

 

DPS is looking for a proven Production Planner to work with a pharmaceutical client in the Boston, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. Previous CMO knowledge is also strongly preferred.

 

Responsibilities:

  • Responsible for assuring supporting all plant production and associated site planning activities as well as material planning, long-and-short term planning in support of commercial manufacturing facility.
  • Develop and maintain site process and long-range planning and capacity utiliz724132.02546ation tools.
  • Ensure the development, revision and accuracy of production plans; ensure key annual, monthly, and weekly production objectives are aligned throughout the organiz724132.02546ation.
  • Develop short- and long-range strategic production plans, resource utiliz724132.02546ation tools material forecasts, and rough-cut capacity; drive disciplined MRP approach within ERP system.
  • Partner with clients and program managers to ensure support of new product introductions including identification and sourcing of new materials, building of BOMs and routings, and development/revise SOPs.
  • Proactively identify, assess, and mitigate operational and organiz724132.02546ational risks; escalate key risks and issues.

 

Qualifications:

  • Bachelors of Science degree in related field.
  • 5+ years’ of GMP-related experience in biopharmaceutical or pharmaceutical manufacturing facilities.
  • Demonstrated ability to manage cross-functional teams and collaborate across client setting.
  • Strong analytical and problem solving skills and great attention to detail.
  • Excellent written and oral communication skills both internal and external.
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