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Qa asst - pharma

Cpl Healthcare
€60,000 - €80,000 a year
Posted: 10 May
Offer description

Job Description

* Provide key support to the QA function within Stability Management, Material Management/Supply Chain and QA support.
* Co-ordination of the Stability Program- Management including study activations, equipment monitoring, stability study approval, activation and receipt of stability study samples and stability unit trend reviews.
* Responsible for the Packaging /preparation of the Product in the Laboratory.
* Responsible for quality-related matters specific to area of responsibility, including any Deviations and associated Investigations
* Generation of Certificates of Analysis/ Conformance to support shipping requirements.
* QA review of laboratory notebooks and logs.
* Assist with reconciliation of laboratory notebooks as required.
* Carry out day to day activities in compliance with site safety policy and procedure.Promote and encourage safe practices and promptly report any safety concerns.
* Provide back up for specific QA Assistant activities as required
* Work effectively within the QA function to deliver on objectives

Key Responsibilities:

* Site stability program co-ordination.
* Co-ordinate with labs to ensure stability sample pulls are performed within outlined pull window and align this with the lab.
* Participating member of a New Product Introduction team of the product’s stability requirements, e.g., stability cabinet/storage capacity, stability simulator, stability specification and time-point requirements.
* Study management for Stability program lots, study timepoint pulls, completion of Stability Studies.Flag the batch, Register the Parent lot and complete Study Activation, Receiving Stability Parent Samples.
* Development of Study Lot Details and creation of Graphics on Darwin Stability Program.
* Study completion and notification to management for final approval
* Monitoring stability units –alarm response, review of temperature/ humidity trends to ensure alarm response/ deviation are complete.
* Materials Management/Supply Chain
* Creation of Certificates of Analysis and Certificates of Compliance for weekly Shipping using various systems and reports, working with Shipping schedule.
* Supporting QA team to ensure Non-Routine Certificate of Analysis are maintained
* Perform COA compliance checks for Consumables and raw materials.

Requirements:

* Hons BSc, MSc, Chemistry, Engineering, Quality, or related discipline, with a minimum of 2 years relevant experience.
* Excellent communication skills in English
* System experience is an advantage: Veeva Vault, Trackwise, Darwin, SuccessFactors, MS Word, Excel, Teams

Feel free to reach out to fatema.aziz@covalensolutions.com for a discussion on this role.

#CplCovalen

#CovalenCpl

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#Cork #Pharma #IrelandPharmaJobs #QAPharma #Pharmajobs #Covalenjobs

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