At a Glance
- Tasks: Manage and maintain pharmaceutical master data with precision in a GMP environment.
- Company: Join a global leader in pharmaceutical manufacturing.
- Benefits: Competitive hourly rate, potential for contract extension, and career growth opportunities.
- Other info: Exciting opportunity with referral incentives and a supportive team culture.
- Why this job: Make a real impact on data integrity and compliance in the pharmaceutical industry.
- Qualifications: Degree in relevant field and 0-3 years of experience preferred.
Pharmaceutical Master Data Specialist – West Lothian, Scotland Opportunity: Do you currently work in a pharmaceutical or a related industry as a Master Data Specialist? Have you used JD Edwards or TrackWise? Are you detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance? If yes then this is the role for you. My client a global pharmaceutical manufacturing company are looking for a Master Data Specialist on a 12 months contract to join their team. You will be responsible for independently executing established Master Data Management processes in a GMP environment. This role focuses on maintaining data accuracy, adhering to established data standards and SOPs, and completing routine master data requests across supported systems. Duties and responsibilities include: * Generating and approving standard Item Masters, Item Branches, and Item Revisions within JD Edwards under established procedures. * Generating and approving Location Masters and Location Master Revisions within JD Edwards under established procedures. * Generating and approving Client Codes and Study Codes within Prisym under established procedures. * Generating and approving Customer and Equipment Setup. * Raising required Change Controls in Global TrackWise to support approved data revisions under established procedures. * Performing assigned master data activities with attention to accuracy, completeness, and required turnaround times. * Analysing and interpreting company and client documentation to determine correct data setup. * Applying established data standards, guidelines, and SOPs in a GMP setting. This is a 12 months contract role based in West Lothian, Scotland which will be reviewed for a possible extension or go permanent dependent on the candidate and business performance. The PAYE rate is between £13.58 - £15.60 per hour. Skills: To apply for the Pharmaceutical Master Data Specialist role you will have the following skills: * Bsc in Biology, Chemistry, Pharmacy, Business, Supply Chain Management, or equivalent professional experience. APICS certification preferred. * 0-3 years of relevant clinical supply, master data, project support, pharmaceutical, biotech, or equivalent business experience preferred. * Detail-oriented and organized with a strong emphasis on data integrity, quality, and compliance. * Computer literate, with experience using spreadsheets, word processing programs, and business system tools. * Willingness to travel preferred. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role
Pharmaceutical Master Data Specialist in Dunfermline employer: Quality Start
Join a dynamic team where your role as a Production Planner and Sales Operations Planner will be pivotal in ensuring the seamless delivery of customer orders. Our company fosters a collaborative work culture that prioritises employee growth, offering training and development opportunities to enhance your skills. Located in a vibrant area, we provide competitive pay and a supportive environment that values innovation and teamwork.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmaceutical Master Data Specialist in Dunfermline
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Quality Start. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Quality Start.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Quality Start. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Quality Start is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Pharmaceutical Master Data Specialist in Dunfermline
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Quality Start!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Quality Start that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Quality Start!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Quality Start, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Quality Start
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Quality Start that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Quality Start’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
