Covingham, Swindon, Wiltshire
14 days ago
Senior Project Manager

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join an outstanding role at Thermo Fisher Scientific Inc. in Swindon, leading innovative projects for a healthier, cleaner, and safer world.

Responsibilities

Lead a core project team for transfer of new, PDS transfer, or internal commercial products.Act as the client's key point of contact for all technical matters through the Technology Transfer process, alongside the allocated Business Manager.Define process scope by supporting the Business Manager and applying internal resources for new client projects during the bidding stage or upon project award.Coordinate and manage projects by defining and agreeing on internal team resources, briefing the team against project scope, and realizing project plans with clear progress monitoring.Lead the customer communications related to Technology Transfer to new clients.Maintain client contact on technical issues and coordinate internal responses with relevant resources.Manage technical information received from clients, collating and disseminating it to the internal team using internal templates.Lead internal and client project teams to reach achievements, recognizing resource needs or delays and bringing up to site management as needed.Scope fiscal requirements related to projects, liaising with internal resources and Business Manager to ensure client agreement and payment.Ensure compliance with GMP requirements, company rules, policies, and procedures.

Eh&s

Understand emergency procedures and align with safe systems of work.Ensure compliance with environment, health and safety policies, rules, signage, and instructions.Ensure timely reporting and investigation of all accidents, near misses, and breaches of rules.

Minimum Requirements/Qualifications

Relevant BSc or equivalent experience with demonstrable experience in the pharmaceutical industry, preferably in the fill/finish operational environment.Strong project management background in production engineering, validation, or quality, with a solid understanding of manufactured dosage forms.Preferred client-facing experience.Strong interpersonal abilities.Dynamic, self-motivated, and proactive approach to challenging assignments.Strong project ownership ethic with a "can do" attitude.Ability to work within and deliver critical timelines.Ability to motivate, communicate, and lead cross-functional teams to deliver project timelines.Outstanding communication skills, both written and oral, with the self-confidence to convince others to buy into proposals and plans.

Join us and make a tangible impact in a world-class organization that values your expertise and ambition. Successfully implement projects and compete with the best in the industry as you help us achieve our mission!

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