Associate, Quality Systems

UK GBR; Croydon; On-site; GBP 35,000 - 45,000; Full time

Job summary

A healthcare company located in Croydon, UK, is seeking a Quality Systems Associate to manage the documentation control process ensuring compliance with regulatory requirements. The ideal candidate has at least 2 years of experience in the pharmaceutical industry and a Bachelor's degree in a relevant field. The role offers opportunities for professional development and emphasizes a healthy work-life balance.

Benefits

Competitive total compensation package

Professional development opportunities

Commitment to work-life balance

Qualifications

• At least 2 years of experience in the pharmaceutical or medical device industry.
• Experience working in a Quality function.
• High level of proficiency in IT systems and data analysis.

Responsibilities

• Manage the UKI Documentation Control process in compliance with requirements.
• Provide training support for documentation control.
• Support audits with necessary documentation.

Skills

Quality management

Data analysis

Documentation control

Change control

Regulatory compliance

Education

Bachelor's degree in Pharmacy or relevant scientific discipline

Job description

This is where your work makes a difference.

At Baxter we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today tomorrow and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together our community is driven by a culture of courage trust and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations and we hold each other accountable for delivering exceptional results.

Here you will find more than just a jobyou will find purpose and pride.

The Quality Systems Associate will provide Quality Systems support to UK and Ireland Compounding organization to ensure that all sites maintain a compliant efficient Quality Management System (QMS) in accordance with local regulatory requirements for Good Manufacturing Practice and Baxter Global QMS requirements and to manage and act as SME for the Documentation Control process.

Reports into the UK Compounding Quality System Manager.

Essential Duties And Responsibilities:

• Responsible for the effective management of the UKI Documentation Control process in compliance with Global and local Regulatory requirements by quality data monitoring and analysis
• Coordinate the content review of the Global Quality Documents in draft stage and the implementation assessment of Global Quality Documents issued with SMEs.
• Execute documentation reviews as required
• Act as Subject Matter Expert for the Documentation Control process (TcU author and Change Specialist 3) & archiving
• Provides Training support as an SME in documentation control and archiving
• Support the trending monitoring and reporting of NCR / CAPA / CQI / CPI in TW8 to facilitate Quality Management Review (QMR).
• Support Internal Corporate external Regulatory and Customer audits through provision of requested documentation records and information in a timely manner
• Other duties in support of Compounding Quality Systems as required including support to Regional / Global Compounding

Experience and Qualifications

• Eligibility required : Resident and eligible to work in the UK on a full-time basis.
• English minimum equivalent to RQF Grade 2 EQF Grade 3 or SCQF Grade 5
• At least 2 years experience in the pharmaceutical or medical device industry.
• Experience working in a Quality function
• Experience of Baxter systems and processes.
• Bachelors degree or higher in Pharmacy or other relevant scientific discipline such as chemistry
• Experience in implementing and maintaining quality systems in a regulated environment including document control change control nonconformance management validation.
• High level of proficiency in IT systems and data analysis and visualization applications
• Experience with other IT systems is advantageous.

What are some of the benefits of working at Baxter

• Competitive total compensation package
• Professional development opportunities
• High importance placed on work life balance
• Commitment to growing and developing an inclusive and diverse workforce

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability / handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If because of a medical condition or disability you need a reasonable accommodation for any part of the application or interview process please click on the link here and let us know the nature of your request along with your contact information.

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Employment Type: Full-Time

Experience: years

Vacancy: 1