Process technician job description (contract) - Dublin

Lawrence Harvey

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Job ID :


Company Type :

Staffing Firms

Industry :


Education Level :


Address 1 :

Western Europe,--Dublin,Dublin,

Key Skills :

Process technician, Dublin, contract, gmp, sop, sops

Salary :


Date Posted :

23 Jul, 2017

Company Name :

Lawrence Harvey

Location1 :


Job Category :

Pharma Manufacturing Jobs

Experience :


Job Type:


Travel Amount:



Job Purpose

* Your role will be in one of the Shift Operating Units where you will be directly involved in the manufacture of one of products, ensuring that they meet all specifications for safety, potency, and efficacy.
* You will work within the guidelines of cGMP to ensure conformance with all regulatory requirements and site SOPs, while assisting in the improvement of all current processes through our Continuous Improvement Program.

Job Responsibilities:

* Responsible for execution of all tasks associated with the preparation for and production of products in cGMP environment ensuring full attention to detail and excellent documentation skills.
* Assist in maintaining a safe, cGMP compliant work environment at all times
* Responsible for completion of tasks according to SOPs and batch records (paper and electronic).
* Perform initial troubleshooting of issues identified during routine operations.
* Assist with the investigation of and operations deviations through QTS system, engaging with all relevant personnel and functions as appropriate.
* Assist where necessary with the training of colleagues in SOPs, process execution and equipment operation.
* Provide input into the creation and maintenance of area SOPs and batch records.
* Seek opportunities for Continuous Improvement.
* Use Lean Tools as part of daily operations (Standard Work, 5S, Method 1, 2 etc) to optimize efficiency and drive the culture of Continuous Improvement and Zero Defects
* Where necessary assist in any in Facility and Equipment start up and Validation activities. Provide input on equipment installation, start-up, operation and troubleshooting to support introduction of new products into sustaining operations.

Essential Education/Experience

To be successful in this role you will require:

* Working knowledge of production operations with a strong focus on attention to detail and compliance to all regulatory standards
* An ability to work independently, and as a member of a team in a dynamic, fast-paced environment that requires flexibility and initiative.
* 1 years' minimum experience in a biopharmaceutical, pharmaceutical, food, dispensing-warehousing cGMP manufacturing or regulated environment, or equivalent.


Certificate, Diploma, Degree, Trade qualification or equivalent is essential

Company Name:

Lawrence Harvey


150 Leadenhall Street,London


Staffing Firms


United Kingdom





100 - 499


Pharmaceutical Recruitment



Phone No. :

0203 327 3072

Lawrence Harvey Life Sciences has exceptional relationships with the top talent and leading organisations in the Pharmaceutical and Medical Devices industry across the UK, USA, DACH region and the rest of Europe. Our consultants are experts within their specific areas and have a deep understanding of the full Life Sciences developmental cycle. As a client with a challenging role or a candidate with a niche specialism, you will receive a consultative service from people who truly understand the expectations and requirements of your industry. In an ever developing industry, an in-depth technical understanding and knowledge adds significant value and is imperative to ensuring our consultants are always up to speed, positioning ourselves perfectly to offer advice, analysis and support to our clients and candidates. We partner with leading pharmaceutical, medical device, generics, biotechnology, clinical research, R&D, manufacturing, regulatory affairs, CRO’s, CMO’s and medical communications organisations and have acquired an enviable and unrivalled reputation for delivering on niche, hard to fill and challenging positions. Our Specialisms within Life Sciences: Pharmaceuticals Medical Devices Regulatory Affairs Quality Assurance Quality Control Engineering Medical Affairs / Medical Information Qualified Persons Drug safety & Pharmacovigilance Biostatistics Clinical SAS Medical Writing Account Management & Business Development

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