At a Glance
- Tasks: Support regulatory submissions and collaborate with teams to meet deadlines.
- Company: Join a leading global pharmaceutical organisation with a focus on innovation.
- Benefits: Competitive pay, hybrid working, and full training provided.
- Other info: Great opportunity for growth in a dynamic and regulated environment.
- Why this job: Kickstart your career in pharmaceutical regulatory affairs with hands-on experience.
- Qualifications: Strong attention to detail, organisational skills, and a proactive attitude.
The predicted salary is between 19.23 - 19.23 £ per hour.
Duration: 12 Months
Location: Sandwich, Kent
Working Hours: 37 Hours per Week
Onsite Requirements: Hybrid Working - Minimum 2.5 Days per Week Onsite
Engagement Type: PAYE or Umbrella Contract
Day Rate / Hourly Rate: PAYE £19.23 per Hour
Legal Right to Work: Applicants must have the legal right to work in the UK. Sponsorship is not available for this position.
Atrium Global is supporting a leading global pharmaceutical organisation in the search for a Regulatory Publishing Coordinator. This is an excellent opportunity for someone looking to develop a career within pharmaceutical regulatory affairs and publishing. Full training will be provided.
We are seeking a highly organised and detail-oriented individual to support the delivery of regulatory submissions to health authorities across global markets. This entry-level opportunity offers exposure to pharmaceutical regulatory publishing processes, systems, and documentation within a highly regulated environment. The successful candidate will work closely with experienced team members to ensure submissions are delivered accurately and on time, whilst supporting the implementation of new digital solutions and maintaining key documentation.
Responsibilities:
- Support regulatory publishing activities to ensure timely and accurate submission delivery.
- Collaborate with internal teams to meet portfolio deadlines and objectives.
- Assist with the implementation of new digital publishing solutions and processes.
- Support business testing and validation activities to ensure compliance and system functionality.
- Maintain and update documentation, training materials, and process records.
- Contribute to continuous improvement initiatives across publishing operations.
- Ensure adherence to quality, compliance, and regulatory requirements.
Requirements:
- Strong attention to detail and accuracy.
- Excellent organisational and time management skills.
- Strong written and verbal communication skills.
- Comfortable working with documentation, systems, and databases.
- Ability to manage multiple tasks and deadlines.
- Proactive attitude with a willingness to learn.
- Interest in pharmaceuticals, healthcare, life sciences, or regulatory affairs.
- Proficient with Microsoft Office applications.
Nice to Have:
- Previous experience within administration, document control, compliance, quality, healthcare, life sciences, or regulated environments.
- Knowledge of pharmaceutical regulatory publishing.
- Awareness of eCTD/CTD submissions, Veeva Vault RIM, Lorenz eValidator, or similar systems.
Regulatory Technical Coordinator in Maidstone employer: Atrium (EMEA)
Atrium Global is an exceptional employer, offering a supportive and collaborative work environment in Sandwich, Kent, where employees can thrive in the dynamic field of pharmaceutical regulatory affairs. With a strong emphasis on employee development, Atrium provides comprehensive training and growth opportunities, ensuring that team members are well-equipped to contribute to innovative digital solutions and compliance initiatives. The hybrid working model promotes a healthy work-life balance, making it an attractive choice for those seeking meaningful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Technical Coordinator in Maidstone
✨Dive into Pharma Networks
Join online communities like PharmaForum or LinkedIn groups dedicated to pharma professionals. Engaging in discussions will not only boost your visibility but can also lead to valuable connections who might tip you off about entry-level gigs, like the one at Atrium (EMEA).
✨Volunteer for Industry Events
Look out for local pharmaceutical conferences or seminars—these are goldmines for making connections and learning what's trending in the industry. Volunteering can also give you a foot in the door and informal chats with recruiters or current employees from companies like Atrium (EMEA).
✨Utilise University Career Services
If you’re still in uni or even recently graduated, tap into your university’s career services. They often have connections with companies looking for bright new interns, especially in pharma—don’t miss out on those resources.
✨Show Off Your Passion and Knowledge
Craft a stellar online presence that reflects your enthusiasm for the pharmaceutical industry—write articles or share insights on platforms relevant to the field. When applying for an entry-level position at Atrium (EMEA), you’ll stand out with demonstrated knowledge on current industry trends.
We think you need these skills to ace Regulatory Technical Coordinator in Maidstone
Some tips for your application 🫡
Show Off Your Science Skills:In the pharmaceutical industry, it's essential to flaunt your scientific knowledge. Make sure to highlight any relevant coursework or projects from your studies that showcase your understanding of drug development or pharmacology in your CV. If you've handled lab work or research projects, mention those too!
Highlight Relevant Certifications:If you’ve got any certifications related to the pharmaceutical field—think Good Clinical Practice (GCP) or any lab safety training—be sure to include those in your application. These can set you apart and show that you’re serious about entering the industry.
Craft a Compelling Cover Letter:Your cover letter is your chance to express your passion for the pharmaceutical industry and your enthusiasm for the role at Atrium (EMEA). Share your motivation for wanting to work in this field and any relevant experiences that set the stage for your entry-level career.
Tailor Your CV for Entry-Level:As you’re applying for an entry-level role, focus on transferable skills that show your potential—like teamwork, effective communication, or analytical thinking. Make sure to keep your CV clear and concise, drawing on your education and any internships, even if they weren't in pharma, to illustrate your readiness for the job!
How to prepare for a job interview at Atrium (EMEA)
✨Know Your Pharma Basics
Brush up on the key concepts and processes within the pharmaceutical industry. Being able to discuss drug development, regulatory processes, or clinical trials can really impress those at Atrium (EMEA) since it shows we have a foundational understanding of the field.
✨Highlight Relevant Coursework and Projects
This is your chance to shine a light on any relevant studies or projects from uni that directly relate to the role. Talk about case studies, lab work, or any experience with pharmaceutical tools or software; this will showcase our hands-on learning and readiness to jump into the role at Atrium (EMEA).
✨Prepare for Technical Questions
Expect some technical questions related to pharmacology, biochemistry, or even basic lab techniques. It's crucial we can talk through methodologies or explain processes confidently; practice might involve reviewing common concepts or having a friend quiz us on them.
✨Show Enthusiasm for Learning
As it's an entry-level role, displaying a thirst for knowledge can set us apart. Talk about how we keep up with industry trends or how we've engaged with pharmaceutical news or journals; enthusiasm can really seal the deal with the hiring team at Atrium (EMEA).
