At a Glance
- Tasks: Design and validate analytical procedures while managing exciting research projects.
- Company: Join a leading laboratory dedicated to patient-driven solutions.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Dynamic role with opportunities for growth and collaboration.
- Why this job: Make a real difference in clinical trials and impact patient care globally.
- Qualifications: BSc in a scientific field and 4 years of lab experience required.
The predicted salary is between 40000 - 50000 £ per year.
SUMMARY
The Research and Development Specialist is responsible for the design, development and validation of analytical procedures, including the study management of method development, validation and investigational studies, ensuring effective implementation.
RESPONSIBILITIES
- Develop validation plans, validation summary reports, stability summary reports, correlation plans and correlation summary reports to meet regulatory requirements.
- Provide supporting information to Scientific Affairs in the evaluation of appropriate testing and/or methodology.
- Liaise with technical staff on feasibility of testing for new study requirements.
- Provide pricing as needed to the Proposals team.
- Select appropriate test methods; research and identify suppliers of laboratory consumables and equipment options for new tests to support clinical trial opportunities.
- Facilitate assay development, conduct instrument validations and implement new testing to satisfy the needs of clinical trials protocols, clients and regulatory requirements.
- Be responsible for assay/panel pre‑validation and validation and correlation testing worldwide.
- Ensure all methods and validations comply with applicable regulatory guidelines, including GCP, GLP, GCLP and CAP.
- Investigate and take corrective action for assay troubleshooting and proficiency testing failures.
- Assess the impact of manufacturer/vendor communications and complete associated documentation.
- Provide study management and direction of laboratory teams for the implementation of analytical method validations.
- Offer consultation and technical support to clinical trials clients and operational staff.
- Manage communications (meetings, calls, audits, etc.) with clients and formulate required responses.
- Prepare SOPs for newly developed test procedures and relevant documentation as necessary.
- Document and own any quality documentation (Note to File, Quality Event, CAPA, deviation, change control) within required time frames.
- Participate in activities ensuring compliance with GCP guidelines and accreditation schemes (e. g., CAP).
- Prepare documentation for and participate in internal and external audits (client and regulatory).
- Comply with policies for the safe, secure and confidential processing and storage of patient/client data and other laboratory information.
- REQUIRED EXPERIENCES
- BSc (or equivalent) or higher in a relevant scientific subject.
- Minimum of 4 years’ experience within a laboratory environment.
- Proven experience with external client interactions and managing deliverables from a laboratory, scientific, or technical standpoint.
- Demonstrable experience managing validation activities within a laboratory setting (clinical laboratory experience highly preferred).
- Strong analytical, problem‑solving and communication skills.
- Highly organized with the ability to manage multiple projects simultaneously.
- Ability to interpret complex technical information and translate findings into clear recommendations.
PHYSICAL REQUIREMENTS
Work is sedentary, with occasional walking or standing.
Exerting up to 10 pounds of force occasionally.
Work involves sitting most of the time, but may include brief periods of walking or standing.
LEGAL DISCLOSURES AND RELATIONSHIP
Rochester Regional Health is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, age, disability, predisposing genetic characteristics, marital or familial status, military or veteran status, citizenship or immigration status, or any other characteristic protected by federal, state, or local law.
At ACM Global Laboratories, we understand that every project we work on, every task we complete impacts patients and their families.
Our dedication to being purposefully patient‑driven is reflected in the high‑quality work provided by our teams every day around the globe.
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Research & Development Specialist employer: 955 ACM UK
ACM Global Laboratories is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of the United Kingdom. With a strong commitment to employee growth, we provide ample opportunities for professional development and training, ensuring that our team members are equipped to excel in their roles. Our focus on quality and adherence to regulatory standards creates a meaningful environment where you can make a significant impact in the field of analytical R&D.
StudySmarter Expert Advice🤫
We think this is how you could land Research & Development Specialist
✨Get Involved in Local Research Communities
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We think you need these skills to ace Research & Development Specialist
Some tips for your application 🫡
Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show 955 ACM UK that you have the hands-on skills they need.
Tailor Your Technical Skills:Make sure to emphasise your technical skills, especially those relevant to the biotechnology sector. Include any software tools or programming languages you've used, like R or Python for data analysis, which could be key for this role at 955 ACM UK.
Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that 955 ACM UK does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.
Include Your Papers and Projects:If you've published any papers or contributed to significant projects, mention them! These documents can boost your application and provide tangible evidence of your expertise in the biotechnology field. Don’t forget to link to any relevant publications or project summaries—this can set you apart from other candidates.
How to prepare for a job interview at 955 ACM UK
✨Brush Up on Lab Techniques
Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at 955 ACM UK. You might even be asked to demonstrate your understanding of these processes.
✨Know Your Bioinformatics Tools
Get comfortable with bioinformatics tools that are commonly used in the industry, like BLAST or Bioconductor. These are key in biotechnology, and having hands-on experience or at least familiarity can set you apart. Prepare to discuss any relevant projects you've worked on, especially if they involved data analysis or genomic research.
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