QC Supervisor
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| Job Type | ContractorFixed Term |
| Area | Sligo, Ireland |
| Sector | ManagementLaboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002869 |
| Job Views | 727 |
- Description
- Team Horizon is seeking a QC Supervisor for our client based in Sligo. As the new Quality Laboratory Supervisor, you will be responsible for ensuring that all raw materials, in-process, finished product, stability and contract testing and is carried out per schedule and records are maintained to appropriate requirements.
As part of this role, you will ensure that technical and systems excellence is maintained in the laboratory by ensuring own skills are maintained, by coaching and training analysts to ensure right first time behaviour and by implementing improved working practices in terms of efficiency, compliance and Right First Time.
You take full responsibility for an assigned segment of the QC operation for example, Raw Materials & Drug Product Analysis or In-process & API.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Ensure Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements.
Understand Regulations and business processes required to maintain Laboratory Data Integrity.
Ensuring timely completion of all laboratory analysis assigned.
Ensuring that analysts working in the assigned cell or team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance.
Improving the overall efficiency and velocity within the assigned team.
Identifying and implementing improvements in analytical practices such as poke yokes.
Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements.
Identifying weaknesses in laboratory performance and working with the laboratory manager to rectify.
Resolving analytical OOS issues as they arise in a timely manner both through practical work and through Soltraqs.
Acting as designee for the Laboratory Manager as assigned
Ensuring 6S excellence is maintained across the Laboratory.
Instilling a quality culture of Zero, Believe it, Achieve it amongst the QC laboratory team
Ensuring that all laboratory test equipment is utilised and maintained correctly.
Executing and / or supporting projects as assigned by the laboratory manager
And any other duties required
What you need to apply:
3rd Level Qualification in na relevant Science discipline
Minimum 4 years analytical experience in the pharmaceutical industry
Proven track record in an analytical role. Must be expert in HPLC, GC,LCMS, GCMS, Automatic titration, Identification techniques.
Strong knowledge on regulatory requirements.
Proficient in using analytical equipment in the QC lab.
Involvement in product transfers / method transfer experience preferred
Good interpersonal and communication skills essential for working across multi-functional teams
