Job Overview
Cpl in partnership with SK pharmteco are seeking to recruit a Quality Control Team Lead to join the QC Department based in Swords, Co.
Dublin on a permanent basis.
About Us
SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland.
We are part of SK Inc., a Korea company with revenues of $99 billion in ****.
Our mission is to 'produce and deliver life-changing therapies that improve patient outcomes and save lives'.
The SK pharmteco Small Molecule, Europe facility located in Swords, Co Dublin, Ireland has led the way in the development, scale-up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years.
With a talented workforce, exceptional technical capabilities and facilities we have made some of the world's most important medicines and continue to do so.
Further information on SK pharmteco can be found at .
Current Need
The Quality Team at the Swords Campus are looking to recruit a Quality Control Team Lead (API) to join the QC Department reporting to the QC Manager.
Position Description
Reporting to the QC Manager, the successful candidate is responsible for stability analysis and Intermediate/API release testing requirements of the site.
They will ensure that this testing is carried out in compliance with local procedures and regulatory requirements.
They will manage a team of senior chemists and analysts and will be responsible for scheduling the work of that team.
The QC Team leader must work to ensure the manufacturing and shipping timelines are adhered to.
Working as part of a Lean Lab team-based structure, the QC Team Lead should have the following attributes:
Ability to lead and motivate people
Openness to change, receptive to new ideas
Strong technical background in chemistry, particularly analytical chemistry
A methodical approach when investigating issues
Knowledge of FDA and European GMP's, particularly pertaining to laboratory operations.
Knowledge / appreciation of other site operations such as QA, R&D, Materials, manufacturing
A BSc in Analytical Science, Chemistry or a related discipline is required.
A minimum of 3 years' experience in analytical chemistry is required.
The desired candidate should be highly motivated, have strong leadership skills, with proven success of leading in a team environment with flexibility to react to changing business needs.
Other Benefits
Excellent opportunities for career enhancement and personal development.
Annual bonus linked to business results.
A well-established further education program.
Employment Type
Full-time (Permanent)
Job Function
Quality Assurance – Pharmaceutical Manufacturing
Industries
Pharmaceutical Manufacturing
EEO Statement
This employer is an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity or age, disability, veteran status or any other basis protected by law.
Application Deadline
Applications are reviewed on a rolling basis until the position is filled.
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