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Quality control team lead

Dublin
Cpl Solutions
Quality controller
Posted: 13 December
Offer description

Senior Talent Specialist with Cpl TEG - Life Sciences
Cpl in partnership with SK pharmteco are hiring
QC Team Lead - Active Pharmaceutical Ingredients
on a permanent contract to join the team in the Swords Campus, North Dublin.
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 Korean 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.
Current Need:
The Quality Team at the Swords Campus is 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
Requirements:
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 in leading in a team environment and flexibility to react to changing business needs
Benefits include:
Excellent opportunities for career enhancement and personal development
Competitive base salary
Annual bonus linked to business results
A well-established further education program
Pension scheme
Private Healthcare
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Manufacturing
Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Cpl by 2x
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