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- Tasks: Assist the Quality Operations team with documentation review and packaging processes.
- Company: Join Thermo Fisher Scientific, a leader in scientific innovation and impactful work.
- Benefits: Enjoy a full-time role with opportunities for growth and development in a global organisation.
- Why this job: Make a difference by supporting vital health and safety initiatives while building your career.
- Qualifications: A-levels or equivalent in relevant subjects; experience in pharmaceutical GMP is essential.
- Other info: Flexible roles available within the Operational Quality team based on business needs.
The predicted salary is between 28800 - 48000 £ per year.
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Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Quality Operations – Associate
At Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture
dedicated to working the right way, for the right reasons – with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.
Position Summary:
This position is responsible for assisting the Quality Operations team with the timely review of documentation and sub functions relating to Clinical or Commercial packaging of pharmaceutical dosage forms in accordance with relevant schedules and agreed timelines working to both Client Specific and internal procedures.
In addition, this role is flexible into additional role(s) within the Operational Quality team. Individuals must complete training and show the capability, competence, experience, and expertise in another Operational Quality related role.
Responsibilities:
- Pre-approval of Clinical/Commercial packaging orders and associated documents
- Post-production review of Clinical/Commercial batch records
- Complete Quality review of Clinical/Commercial supporting documentation
- Resolution of client observations on batch records following post-production review
- Assist with archiving of Clinical/Commercial batch records
- Support external customer related discussions on explaining internal processes for onboarding/audit related activities
- Flex and perform other Operational Quality role(s) based on business need
- Perform other related additional duties as requested by the Quality Operations – Team Leader
Education/Qualifications:
- Essential: A-level or equivalent in relevant subjects
- Essential: Experience in pharmaceutical GMP
- Desirable: Degree level or equivalent in relevant subjects
Experience:
- Desirable: Solid understanding and proven experience with GxP pharmaceutical packaging activitie
Knowledge, Skills, Abilities:
- Essential: High degree of accuracy, concentration, verbal and written communication
- Essential: Cooperation with inter/intra department teams to overcome challenges and provide support to other colleagues
- Essential: Ability to prioritise own workload to deliver personal and team objectives within set timeframes
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Quality Assurance, Product Management, and Engineering
-
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Quality Operations - Associate employer: Thermo Fisher Scientific
Contact Detail:
Thermo Fisher Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Operations - Associate
✨Tip Number 1
Familiarise yourself with the specific quality standards and regulations in the pharmaceutical industry, particularly GMP. This knowledge will not only help you understand the role better but also demonstrate your commitment to quality during any discussions.
✨Tip Number 2
Network with current or former employees of Thermo Fisher Scientific on platforms like LinkedIn. Engaging with them can provide valuable insights into the company culture and expectations, which can be beneficial during interviews.
✨Tip Number 3
Prepare to discuss your experience with documentation and batch records in detail. Be ready to share specific examples of how you've ensured accuracy and compliance in previous roles, as this is crucial for the Quality Operations position.
✨Tip Number 4
Showcase your ability to work collaboratively by preparing examples of how you've successfully worked within teams to overcome challenges. Highlighting your teamwork skills will resonate well with the company's emphasis on cooperation.
We think you need these skills to ace Quality Operations - Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Quality Operations - Associate position at Thermo Fisher Scientific. Understand the responsibilities and qualifications required, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasise any experience you have in pharmaceutical GMP or related fields. Mention specific tasks you've performed that align with the responsibilities listed in the job description.
Showcase Your Skills: Make sure to highlight your skills in accuracy, communication, and teamwork. Provide examples of how you've successfully collaborated with others or managed your workload to meet deadlines in previous roles.
Craft a Strong Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also expresses your passion for the role and the company. Explain why you want to work at Thermo Fisher Scientific and how you can contribute to their mission.
How to prepare for a job interview at Thermo Fisher Scientific
✨Understand the Role
Make sure you thoroughly read the job description and understand the responsibilities of a Quality Operations Associate. Be prepared to discuss how your skills and experiences align with the specific tasks mentioned, such as documentation review and client interactions.
✨Showcase Your Attention to Detail
Since this role requires a high degree of accuracy, be ready to provide examples from your past experiences where your attention to detail made a significant impact. This could include instances where you identified errors or improved processes.
✨Prepare for Technical Questions
Brush up on your knowledge of pharmaceutical GMP and GxP practices. Expect technical questions related to these areas, and be ready to explain how you've applied this knowledge in previous roles or projects.
✨Demonstrate Team Collaboration Skills
The role involves cooperation with various teams, so be prepared to discuss how you've successfully worked in team settings. Share specific examples of how you overcame challenges together and supported your colleagues.
