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CMC Project Manager

Job in Huron, Beadle County, South Dakota, 57350, USA
Listing for: Scientific Search
Full Time position Listed on 2026-11-05
Job specializations:
Salary/Wage Range or Industry Benchmark: 83000 - 124000 USD Yearly USD 83000.00 124000.00 YEAR

Job Description & How to Apply Below

CMC Project Manager - Contract

Location: Remote
Duration: 3-6 months

An innovative, rapidly growing biotechnology company is seeking an experienced CMC Project Manager
. This position will support technical teams and manage associated projects both in house and at CDMO's. The successful candidate will have a strong understanding of the functional operations of Chemistry, Manufacturing, and Controls with a focus on antibodies and proteins in general.

Responsibilities
  • Develop and maintain integrated project plans, timelines, and milestones trackers
  • Coordinate project activities across Technical Operations, Process Development, Analytical Development, Quality, Regulatory, Supply Chain, and Manufacturing teams
  • Monitor financial approval cadence closely and coordinate budget management within teams
  • Coordinate CMC team meetings coordinating with CMC leads, including assembly of agendas and meeting minutes
  • Ensure effective cross-function and cross-project communications in and out of internal development teams
  • Support technical leads with vendor management but not limited to contract review and negotiation, timeline management, and quarterly business review meetings.
  • Collaborate with finance to forecast and manage the budget and quarterly accrual for all tech ops activities
  • Support tech ops with Request for Proposal, contracts, POs and invoice approvals.
Requirements
  • B.S. degree is required in Science, Engineering or related field with at least 10+ years relevant industry experience in biopharma
  • A minimum of 3-5+ years project management experience as designated project manager or PM responsibilities as part of a technical role
  • Working knowledge of small molecules and biologics process development, analytical development, GMP manufacturing and quality control testing
  • PMP certification is a plus
  • Ability to accommodate flexible working hours to support business relationships in different time zones
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