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- Tasks: Develop and validate bioassay methods while ensuring compliance with industry standards.
- Company: Leading pharmaceutical solutions provider focused on innovation and quality.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: BSc in a scientific discipline and 2 years of analytical experience required.
- Other info: Collaborative environment with a focus on continuous improvement and career development.
The predicted salary is between 36000 - 60000 £ per year.
Business: Pharma Solutions
Department: Analytical Development
Location: Grangemouth
Reporting Structure: Reports to Bioassay Team Manager
Role Overview
Scientist responsible for the method development, qualification/validation, technical transfer, stability and QC release testing within the Bio-Assay team.
Key Responsibilities
- Establish own day to day priorities. General guidance and long-term objectives are provided by the Bio-Assay Senior team.
- Provide project support for routine Bio-Assay QC and stability testing, method development, technical transfer and validation activities according to defined SOPs and protocols and in compliance with best cGMP working practices and techniques.
- Check and review data in compliance with Data Integrity requirements.
- Maintain laboratory areas, ensuring procedures are complied with to meet client, regulatory, GMP and safety requirements. Be accountable for the bioassay laboratories being clean, tidy and well-organised and in a state of continuous inspection readiness.
- Execute calibration of equipment and instruments, informing relevant personnel in a timely manner of any failure of calibration. Carry out general maintenance and housekeeping of equipment. Ensure that at any time equipment, facilities and materials used in the area of responsibility comply with defined standards.
- Provide training and troubleshooting support to Development and Quality Control groups as required.
- Engage in specified compliance and improvement projects.
- Workload planning with other staff to ensure required timelines are met.
- Provide cover for other Bio-Assay Scientists as required.
- Have ownership and ensure timely close out of deviations, investigations, change controls and commitment tracking. Immediately escalate and report deviations to materials, facilities, processes or procedures to Bio-assay and QC management.
- Assist Bio-Assay team in the implementation of measures and targets: Ensure economic use of labour, materials, energy and services, proposing and implementing measures for cost reduction and waste minimisation to meet the department and site targets.
- Support and provide training of new members of staff to the company/department.
- Apply best cGMP work-practices and techniques to manage the testing and release bulk drug substance, final products and stability products within specification and in accordance with Data Integrity requirements, Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data.
- Uphold cGMP principles and ESH standards in his/her area of responsibility, continually seek opportunities to improve and enhance standards, and encourage other staff to do likewise.
- Provide Bio-assay project support, have involvement in decisions on scheduling of release, stability, development, technical transfer and validation in conjunction with other technical staff.
- Identify opportunities for improved methods of working to enhance efficiency, cost control and safety/GMP performance.
- Assist in the introduction of new equipment by supporting IQ/OQ/PQ and comparison studies where applicable.
- Be the system owners of Bio-Assay equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Bio-Assay department.
- Write and update of SOPs, instructions and protocols and other documentation.
- Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.
Essential Qualifications:
- BSc in a relevant Scientific discipline or equivalent.
Essential Experience:
- A minimum of 2 years analytical experience, with a sound working knowledge of GMP & SHE standards and safety matters together with highly developed interpersonal and team building skills.
Bioassay Scientist in Falkirk employer: Piramal Group
Contact Detail:
Piramal Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Bioassay Scientist in Falkirk
✨Tip Number 1
Network like a pro! Reach out to professionals in the bioassay field on LinkedIn or at industry events. A friendly chat can lead to job opportunities that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by practising common questions related to bioassay techniques and GMP standards. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 3
Showcase your skills! Bring examples of your previous work, like reports or presentations, to interviews. This will help you stand out and demonstrate your expertise in method development and validation.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are genuinely interested in joining our team.
We think you need these skills to ace Bioassay Scientist in Falkirk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Bioassay Scientist role. Highlight your experience with cell-based assay techniques and any relevant analytical work you've done. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background aligns with our needs. Don’t forget to mention your understanding of GMP standards and your commitment to quality.
Showcase Your Attention to Detail: In the bioassay field, attention to detail is crucial. Use specific examples in your application that demonstrate your ability to follow protocols accurately and maintain data integrity. We love candidates who can show us they care about the little things!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining the StudySmarter team!
How to prepare for a job interview at Piramal Group
✨Know Your Bioassays
Make sure you brush up on your knowledge of cell-based assay techniques and the specific methodologies relevant to the role. Be prepared to discuss your previous experience with method development and validation, as well as any troubleshooting you've done in the lab.
✨Understand cGMP Standards
Familiarise yourself with current Good Manufacturing Practices (cGMP) and how they apply to bioassay testing. Be ready to explain how you've adhered to these standards in your past roles and how you would ensure compliance in this new position.
✨Showcase Your Attention to Detail
Since this role requires a high level of accuracy, be prepared to provide examples of how you've maintained data integrity and ensured quality in your previous work. Highlight any experiences where your attention to detail made a significant impact on project outcomes.
✨Be a Team Player
This position involves collaboration with various teams, so demonstrate your interpersonal skills. Share examples of how you've successfully worked within a team, provided training, or supported colleagues in achieving common goals. This will show that you're not just a great scientist, but also a valuable team member.
