Job Description

Immediate need for a talented Technical Leader, MSAT CMC Development/ Project Manager. This is a 26+months contract opportunity with long-term potential and is located in Cambridge, MA (Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID:25-84033

Pay Range: $60 - $65/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Manager Intakes: core business hours, onsite 3 times a week/flexible, track progress of project, review data, write reports, review reports, provide feedback on technical and scientific aspects of the project, looking for someone with small molecules exp not vaccines, not antibodies, not biologics, need to have technical experience with small mol.
• Someone who can work independently and within team, small team but they are very cohesive and work together well.
• BS/MS in chemistry, pharmacy or science with strong experience in Pharmaceutical development, specifically oral dosage form for small molecules, technical operations and /or manufacturing.
• MBA a plus. Travel reimbursed - not expecting much travel but here and there might be a tiny bit, Not expecting it to be 20%. Maybe a team meeting or two in Morristown if the big wigs are in town.
• Like to haves: 1. Veeva is a plus 2. Regulatory applications/documents 3. French speaking would be a benefit.
• Executes 2nd generation program technical strategies to the MSAT Technical Product Team, focused on pharmaceutical development of oral dosage forms for small molecules.
• Implements product control strategies.
• Provides technical support to manufacturing sites for significant deviations and drives process and product life cycle management improvements for process robustness and yields.
• Select appropriate QbD strategies, process parameter risk assessments, application of prior knowledge.
• Drafts product- and process specific technical reports to support life-cycle management activities.
• Supports MSAT Program Directors and CMC Leaders with planning, coordinating and following activities for the various types of projects outlined above, organizing meetings and preparing project updates for project teams and M&S management. Specific duties and responsibilities include, but not limited to:
• Creating project scope documents to gain sponsor and management approval.
• Creating and maintaining detailed timelines and project plans with input from Program Directors / CMC Leaders.
• Organizing meetings with project teams for status update and action item follow up to ensure adherence to timelines.
• Organizing meetings with sponsors (R&D, GBU, M&S Teams) to communicate project updates.
• Conducting risk assessments for project activities and outlining contingency plans.
• Creates and maintains detailed project plans with gating / milestones.
• Prepares summaries of proposals from CMOs/CROs for projects and presents to management for review.
• Obtains the necessary technical information to support projects at internal Client sites or CMO/CROs.
• Assists with reviewing and finalizing technical documents such as protocols, reports and regulatory dossier content.
• Assists with reviewing contracts (such as CDSs, MSAs, Quality Agreements) and quotations to support CMC development projects, Industrial technical projects and internal Industrial Development programs.

Key Requirements and Technology Experience:

• Key Skills: Small Molecule, Project Management, data review, dosage .
• BS/MS in chemistry, pharmacy or science with strong experience in Pharmaceutical development, specifically oral dosage form for small molecules, technical operations and /or manufacturing. MBA a plus.
• Proficiency in MS Office
• Knowledge of project management software
• Solid writing and presentation skills
• Excellent organizational and communication skills.
• At least 7+ years’ experience in technical project management, relevant pharmaceutical development, technical operations and/or manufacturing of various drug product dosage forms for small molecules.
• Must have prior experience as a project manager of technical projects with demonstrated ability to facilitate multi-disciplined teams.
• Experience with international project teams a plus.
• Quality and/or Regulatory background also highly desirable.
• Knowledge of French language (speak, read and/or write) a plus.
• Open to travel up to ~20% of the time.
• Job based in Cambridge, MA, with on-site presence in compliance with Client policy.

Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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