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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 SOPs, instructions and protocols and other documentation.
- Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.
- Release, Stability, Development, technical transfer and validation.
- Troubleshooting.
- Deviation, change control and commitment tracking close out.
Key Competencies:
- Experience / expertise in cell‑based assay techniques
- Ability to follow instructions accurately
- Attention to detail
- Reliability and effective communication
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 (FTC) in Falkirk employer: Piramal
Contact Detail:
Piramal Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Bioassay Scientist (FTC) in Falkirk
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma industry, especially those who work in bioassays. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and understanding of cGMP practices. We recommend practising common interview questions related to method development and QC testing to show you're the right fit for the Bioassay Scientist role.
✨Tip Number 3
Showcase your problem-solving skills! Be ready to discuss how you've tackled challenges in previous roles, especially around troubleshooting and deviation tracking. This will highlight your ability to handle the responsibilities of the position.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our team at StudySmarter.
We think you need these skills to ace Bioassay Scientist (FTC) in Falkirk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Bioassay Scientist role. Highlight your analytical experience, especially in cell-based assay techniques, and any relevant GMP knowledge. We want to see how you fit into our team!
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 attention to detail and reliability – these are key for us!
Showcase Your Team Spirit: We love team players! In your application, share examples of how you've collaborated with others in previous roles. Whether it's training new staff or working on compliance projects, let us know how you contribute to a positive team environment.
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’s super easy – just follow the prompts and submit your materials!
How to prepare for a job interview at Piramal
✨Know Your Bioassays
Make sure you brush up on your knowledge of cell-based assay techniques and the latest trends in bioassay development. Be ready to discuss specific methods you've used and how they align with the company's focus on cGMP practices.
✨Showcase Your Attention to Detail
During the interview, highlight examples where your attention to detail made a difference in your previous roles. Discuss how you ensure compliance with Data Integrity requirements and how you maintain high standards in laboratory practices.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations, like troubleshooting a failed calibration or managing a deviation. Think through your past experiences and be ready to explain your thought process and actions clearly.
✨Demonstrate Team Spirit
Since collaboration is key in this role, be prepared to talk about how you've supported team members in the past. Share instances where you provided training or helped improve processes, showing that you're a team player who values collective success.
