Head of Gmp Analysis - Cwmbran, United Kingdom - AptarGroup, Inc.

AptarGroup, Inc.
AptarGroup, Inc.
Verified Company
Cwmbran, United Kingdom

1 week ago

Tom O´Connor

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Tom O´Connor

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Description

Date:
Mar 15, 2023


Location:
Cwmbran, Wales, GB, NP44 3WY


Company:
Aptar Group


Job Opportunity - Head of GMP Analysis

Who we are

At Aptar, we use insights, design, engineering and science to create innovative packaging technologies that build brand value for our customers, and, in turn, make a meaningful difference in the lives, looks, health and homes of people around the world.


Every day, Aptar creates "a-ha moments" for its customers and their consumers and patients by continually bringing innovations to market that convert non-dispensing packaging into breakthrough product-dispensing systems, including those that give people more effective ways to put on their favourite fragrance, kids the opportunity to pour ketchup without making a mess and patients connected technologies that help them more easily adhere to treatment.


We have manufacturing facilities in North America, Europe, Asia and South America and over 14,000 dedicated employees in some 20 countries.


You should work here because we:

  • Attract and develop high performing people.
  • Promote a diverse and inclusive work environment.
  • Allow for failure by allowing people to make mistakes through an open and trusting environment.
  • Invest in the development of employees through local, regional and global career opportunities.
  • Contribute to the communities where we reside.

What's new with Aptar
We have an exciting position open at Nanopharm, which is an

Aptar Pharma Company:
Head of GMP Analysis, reporting to our Chief Operations Officer.

This is how your journey begins:

Role Overview

  • To lead and manage the GMP Analysis Pharmaceutical Development Unit (PDU) groups at Nanopharm.
  • The GMP Analysis group is tasked with:
  • Completing work packages for customers/sponsors to cGMP standard
  • Ensuring high quality/integrity of the data and reports, including regulatory submission documents
  • Conducting studies either intended for regulatory submission, in vitro bioequivalence studies (e.g. SmartTrack) or clinical product release testing.
  • To lead, manage and oversee the delivery of the GMP Analysis revenue generation, portfolio of work for our customers, internally and externally, efficiently and effectively.
  • To support and oversee the organisation and planning of the daytoday project activities with the use of the most effective equipment and resources dependent on customer requirements.
  • To support the Chief Operations Officer (COO) with ensuring the Nanopharm organisation achieve its commercial goals for the GMP Analysis function, adhering to all industry rules/regulations and legislation, whilst developing robust policies/governance and supporting our team members in every aspect of their work.
  • Support the COO with establishing and delivering a vision, business strategy and associated GMP Analysis departmental goals over several years timeframe.
  • Overseeing the GMP Analysis groups technical operations of the organisation and taking necessary decisions/changes to meet business goals/objectives. Working with the COO to establish robust forecasts and plans to ensure the delivery of commercial expectations.
  • Collaborate with other departments, including Project Management, Quality and Operations to define, prioritise and progress projects.
  • Manage and control the operational budgets to ensure that the company has all the resources required to meet its objectives within agreed financial parameters and to maintain the financial strength of the company.
  • Work with the COO to establish the organisations operational processes and lead continuous improvement of them, enhancing profitability, efficiency, customer service and staff health/safety/wellbeing.
  • Empowering the GMP Analysis team with the leadership and resources they need to successfully complete operations initiatives.
  • To lead Nanopharm forward as a member of the Senior Leadership Team (SLT).
  • To enhance the capabilities and reputation of Nanopharm continuously.
  • To ensure compliance with HS&ES (Health & Safety and Environmental Sustainability), HR (Human Resources), Quality and Financial regulations, policies and procedures at Nanopharm, for you and your team.

Live our Values
Ensure you are an advocate and role model for exemplary performance aligned to the Aptar / Nanopharm Values in everything you do:

  • We Respect and Trust People-
  • We belive in the value of each individual-
  • We challenge ourselves to take initiative and develop our full potential-
  • We promote teamwork and cooperation at all levels-
  • We strive for relationships that are based on openness, honesty and feedback-
  • We act ethically and responsibly, holding ourselves accountable to all stakeholdersJob Details / Responsibilities
  • Job descriptions cover approximately 85% of a role and are not an exhaustive list of responsibilities and duties. You are expected to carry out other activities that are within reasonable scope of the role._
Health Safety & the Enviro

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