11 days old

Potency Quality Analyst

Pfizer
Grangeville, ID 83530
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Closing date for applications: 15th June 2021



Are you an experienced Potency Quality Analyst looking for your next step within a state-of-the-art manufacturing plant? If so, Pfizer Grange Castle has a permanent, full-time opportunity for you!



Pfizer Grange Castle manufacturing site, one of the largest integrated biopharmaceutical plants in the world is seeking a number of contract and permanent QC analysts.



The Quality department is an expanding and diverse team currently comprised of ~500 people, over 12 different areas each with a multitude of high performing teams across both QA and QC. You will contribute to the safe operations of QC Laboratories, support QC testing, transfers and projects for both established and upcoming new products in Pfizer Grange Castle and facilitate and assist with laboratory investigations.



**What We Offer?**



Permanent position with Competitive Salary and Shift Allowance plus Bonus Schemes, Healthcare for you & your family, Pension & Share Scheme, Long term Income Protection, Life Assurance, Option to buy Additional Annual Leave days.



Grange Caste is close to the M50 and offers free parking and subsidized canteen onsite.



**Our Culture**



Our Culture in Grange Castle is hugely important to us. We recognize that people are the cornerstone of Pfizer's success. We embrace career development & colleague engagement. As a team, together we run our business, so your input and expertise are essential to our success!



We run regular EXPOs onsite such as Kids 2 Work Day, Day in the Life and Health and Wellbeing initiates. We have a Site Culture Team and a varied Sports and Social Club.



Our safety is at the heart of everything we do. We strive to be free of injuries and incidents because we care about everyone here



Our culture is founded on the pillars of Equity, Joy, Courage and Excellence



**About the Role**



**QC Analyst,Potency**



+ Contribute to the operation of QC Laboratories

+ Follow and assist in the creation, review and maintenance of SOP's for cGMP lab test procedures and systems

+ Facilitate and assist with laboratory investigations

+ Facilitate and assist with corrective action tasks

+ Ensure safe operations, attention to detail and good documentation skills according to cGMP

+ PerformroutinePotency/Cell Culture Tasks including but not limited to:



+ Performing cell-based assays such as cell proliferation and apoptosis assays to support release and stability testing.

+ Performing In Vitro Relative Antigenicity Assays to support release and stability testing.

+ Preparation and Qualification of Critical Reagents.



+ Review of lab testing results.

+ Media preparation and reagent qualification

+ Establish and Maintenance of Cell Line folders

+ Cell Banking and Qualification

+ Cell Revival

+ Cell Passaging of both adherent and suspension cell lines

+ Cell Counting

+ Waste inactivation



+ Assist in the running of thePotency/cell culture lab including weekly ROTA preparation, inventory checks, expiry checks, logbook review, waste maintenance and consumables and stock checks

+ Support the management of contract lab testing.

+ Support and assist in the introduction of new Cell Lines

+ Support the creation of new LIMS builds for new Cell Lines/Assays

+ Ensure supply of cells and other critical reagents to external labs as required

+ Assist in the maintenance and development of training programs and perform training of other analysts

+ Maintain established 5S process and assist in the 5S audits and related activities

+ Support and assist the continuous improvement projects and all related CI activities

+ Perform and assist in additional duties as directed by the Supervisor.

+ Report and document any non-conformances to the Supervisor.



**Education/Experience:**



+ **Minimum of 3 years' experience necessary in a QC Potency position.**

+ **Shift work may be required for this role**



How to apply



Make a difference today, all suitable candidates should apply though the link with CV provided by COB 15th April 2021. We are looking forward to hearing from you!

In order to be considered for this position you need to be legally eligible to work in Ireland.

Due to high volume of applications we will be contacting successful candidates only.



+ Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.



\#LI-PFE



**Additional Information**



+ In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.

+ Please note there is no relocation support available for this position



**How to apply**



+ Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you!



Purpose



**Breakthroughs that change patients' lives** ... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.



Digital Transformation Strategy



One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.



Equal Employment Opportunity



We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.



Quality Assurance and Control



\#LI-PFE
Posted: 2021-06-02 Expires: 2021-07-05
Sponsored by:
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Potency Quality Analyst

Pfizer
Grangeville, ID 83530

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