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- Tasks: Develop and validate bioassay methods while ensuring compliance with GMP standards.
- Company: Leading Pharma Solutions company focused on innovation and quality.
- Benefits: Competitive salary, professional development, and a collaborative work environment.
- Why this job: Join a dynamic team making a real impact in pharmaceutical development.
- Qualifications: BSc in a scientific discipline and 2 years of analytical experience required.
- Other info: Opportunity for career growth and involvement in exciting projects.
The predicted salary is between 36000 - 60000 £ per year.
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 any 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 of 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.
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 Pharma Ltd
Contact Detail:
Piramal Pharma Ltd 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 professionals in the bioassay field on LinkedIn or at industry events. A friendly chat can lead to opportunities 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 want you to showcase your expertise and how it aligns with the role!
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer’s mind and show your enthusiasm for the position.
✨Tip Number 4
Apply through our website for the best chance of landing that job! We love seeing candidates who take the initiative to connect directly with us.
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 is tailored to the Bioassay Scientist role. Highlight your experience in method development, QC testing, and any relevant GMP knowledge. 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 bioassays and how your background makes you a great fit for our team. Keep it concise but engaging – we love a good story!
Showcase Your Attention to Detail: In the world of bioassays, attention to detail is key. Make sure to mention specific examples from your past work where your meticulous nature made a difference. We appreciate candidates who understand the importance of accuracy!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining the StudySmarter family!
How to prepare for a job interview at Piramal Pharma Ltd
✨Know Your Bioassays
Make sure you brush up on your knowledge of cell-based assay techniques and the specific methods relevant to the role. Be prepared to discuss your previous experience with method development and validation, as well as any challenges you've faced in QC testing.
✨Understand cGMP Standards
Familiarise yourself with current Good Manufacturing Practices (cGMP) and how they apply to bioassay work. Be ready to explain how you've implemented these standards in past roles and how you ensure compliance in your daily tasks.
✨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 meticulous record-keeping in your previous positions. Highlight any specific instances where your attention to detail made a significant impact.
✨Be Ready for Team Dynamics
This position involves collaboration with various teams, so think about how you've worked effectively within a team in the past. Prepare to discuss your communication skills and how you've supported colleagues in training or troubleshooting scenarios.
