At a Glance
- Tasks: Join us as a QA Associate, ensuring top-notch quality in health products daily.
- Company: Cencora Alloga UK is a leading global pharmaceutical solutions company dedicated to healthier futures.
- Benefits: Enjoy a full-time role with competitive salary and opportunities for personal growth.
- Why this job: Make a real impact in health while working in a supportive and innovative environment.
- Qualifications: A-level education preferred; 3 years in validation within GDP or GMP is a plus.
- Other info: Flexible work approach and strong attention to detail are essential for success.
The predicted salary is between 24000 - 36000 £ per year.
QA Associate – Validation (Alloga UK) page is loaded
QA Associate – Validation (Alloga UK)
Apply locations South Normanton, United Kingdom time type Full time posted on Posted 8 Days Ago job requisition id R259754
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
Job Details
Are you a detail-oriented professional with a passion for quality assurance?
Cencora Alloga UK, is looking for a dedicated QA Associate – Validation to join our team. In this role, you will be instrumental in supporting our compliance with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) regulations. Your focus will be on ensuring that all work is executed safely, efficiently, and to the highest quality standards set by our company, clients, and regulatory bodies.
Location: South Normanton, Derbyshire, UK
Salary: £28,986.96
Working Hours: Monday to Friday, 9:00 AM – 5:00 PM
Company: Cencora Alloga UK
Key Responsibilities:
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Over-arching Principles of Working:
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Report all accidents and near misses immediately to the Health & Safety Manager.
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Conduct QA activities according to company procedures and client instructions.
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Document all QA activities accurately.
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Validation Responsibilities:
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Develop and maintain the site Validation Master Plan (sVMP).
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Create validation and qualification protocols.
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Execute qualification and validation activities in line with the sVMP.
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Conduct qualification and validation of quality-critical assets following applicable change controls.
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Accurately record all qualification and validation activities and report weekly performance measures.
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Compliance Responsibilities:
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Stay updated on relevant regulations.
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Ensure QA activities comply with defined procedures and client instructions while maintaining appropriate records.
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Record, investigate, and communicate quality incidents, client/customer complaints, and deviations.
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Ensure timely completion of corrective actions.
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Manage quality documents to ensure they are approved, controlled, and reviewed correctly.
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Prepare for and participate in audits, providing supporting data for quality decisions.
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Additional Responsibilities:
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Review daily and monthly temperature trending.
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Participate in client and regulatory audits.
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Maintain records of QA activity and complete key performance indicators (KPIs) relevant to the role.
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Archive paperwork and manage the removal of TMDs for destruction.
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Conduct periodic internal compliance inspections to identify improvement opportunities.
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Competencies:
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Effective communication at all levels within Cencora Alloga UK and with clients.
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Ability to influence through rational arguments and compromise when necessary.
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Maintain composure under pressure and focus on problem resolution.
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Build and maintain harmonious working relationships with clients and colleagues.
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Demonstrate initiative, ownership, and task completion.
Personal Attributes:
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Flexible approach to work with strong planning and prioritisation skills.
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Confident, enthusiastic, respectful, and exhibits integrity.
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Willingness to learn from mistakes and make sound decisions.
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Drive for success and self-development, with a conscientious attitude toward performance improvement.
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Excellent attention to detail.
Knowledge, Skills, and Experience Required:
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Ideally educated to A-level or equivalent.
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3 years\’ experience in a validation role within a GDP or GMP environment would be highly desirable
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Understanding of GDP and GMP regulations, as well as ISO 9001.
What Cencora offers
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.
Full time
Affiliated Companies
Affiliated Companies: Alliance Healthcare Management Services Limited
Equal Employment Opportunity
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com . We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned
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About Us
Cencora is a leading global pharmaceutical solutions company that is committed to improving the lives of people and animals everywhere. We connect manufacturers, providers, and patients to ensure that anyone can get the therapies they need, where and when they need them.
We’re a purpose-driven organization, where all of our team members around the world are united in our responsibility to create healthier futures. We work together every day to help our partners bring their innovations to patients worldwide, creating unparalleled access and impact at the center of health.
Job Scams
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1.) Research the Company: Thoroughly research any company before applying or sharing personal information, check their website, read reviews, and verify their legitimacy.
2.) Be Wary of Unrealistic Promises: Exercise caution If a job posting offers high salaries and minimal qualifications. Legitimate jobs will have realistic expectations and provide detailed job requirements. Jobs at Cencora can be found on Cencora.com/careers
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QA Associate - Validation (Alloga UK) employer: AmerisourceBergen
Contact Detail:
AmerisourceBergen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Associate - Validation (Alloga UK)
✨Tip Number 1
Familiarise yourself with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) regulations. Understanding these standards will not only help you in the interview but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in QA roles. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios related to quality assurance and validation. Think of examples from your past experience where you successfully handled compliance issues or improved processes.
✨Tip Number 4
Showcase your attention to detail during any interactions with the company. Whether it's through your communication or how you follow up after applying, demonstrating this trait can set you apart as a strong candidate for the QA Associate role.
We think you need these skills to ace QA Associate - Validation (Alloga UK)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the QA Associate - Validation position. Tailor your application to highlight relevant experience in quality assurance, particularly in GDP and GMP environments.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous roles or projects that demonstrate your experience with validation processes, compliance with regulations, and attention to detail. Use specific examples to illustrate your skills.
Craft a Strong Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also conveys your passion for quality assurance and your desire to contribute to Cencora's mission of creating healthier futures. Make it personal and engaging.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a QA role.
How to prepare for a job interview at AmerisourceBergen
✨Understand GDP and GMP Regulations
Make sure you have a solid grasp of Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) regulations. Be prepared to discuss how these principles apply to the role and provide examples from your past experience.
✨Showcase Your Attention to Detail
As a QA Associate, attention to detail is crucial. During the interview, highlight specific instances where your meticulous nature helped prevent errors or improved processes in previous roles.
✨Prepare for Compliance Questions
Expect questions related to compliance and quality assurance activities. Familiarise yourself with common compliance challenges and be ready to discuss how you would handle them, demonstrating your problem-solving skills.
✨Demonstrate Effective Communication Skills
Effective communication is key in this role. Be prepared to discuss how you've successfully communicated with team members and clients in the past, especially in high-pressure situations or during audits.