Analytical Development Scientist

Piramal Group; Falkirk; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading company in pharmaceutical science seeks an Analytical Development Scientist in Falkirk. The role includes ensuring compliance with GMP standards, engaging in project deliveries, providing team support, and maintaining high-quality operations. Candidates should demonstrate effective communication and problem-solving skills within a collaborative environment.

Responsibilities

• Perform assigned work ensuring efficient use of time to complete objectives.
• Provide training to QC groups and maintain laboratory areas.
• Ensure timely project deliverables and support method development.

Job description

Social network you want to login/join with:

Analytical Development Scientist, Falkirk

Client:

Piramal Group

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

4b924e31989c

Job Views:

2

Posted:

29.06.2025

Expiry Date:

13.08.2025

Job Description:

Key Roles/Responsibilities:

Departmental Operations:

• Perform assigned work as agreed with the project lead and/or Analytical Development Manager, ensuring efficient use of time to complete objectives.
• Maintain laboratory areas, ensuring procedures meet client, regulatory GMP, and safety requirements.
• Provide training and troubleshooting support to production and stability Quality Control groups.
• Support QC activities as required.
• Engage in compliance and improvement projects.
• Provide cover for other Analytical Development Scientists as needed.
• Use resources economically, proposing measures for cost reduction and waste minimization.
• Identify opportunities for improved working methods to enhance efficiency, safety, and GMP performance.
• Support training of new staff members.

Project Delivery:

• Ensure timely completion of project deliverables.
• Lead project aspects as appropriate.
• Plan and execute work to meet project timelines and customer requirements.
• Support method development, transfer, qualification, and validation activities.
• Assist in the introduction of analytical methods into QC, production, and stability groups.
• Plan workload with team members to meet deadlines.
• Support QC activities if needed.
• Communicate professionally with clients.

Quality:

• Close out deviations, change controls, and commitments promptly.
• Uphold cGMP and ESH standards, seeking continual improvement.
• Record work accurately in official notebooks and compile reports.
• Follow protocols and procedures diligently.
• Ensure raw data and interpretations are accurate.
• Teamwork: Work cooperatively with others.
• Communication: Keep relevant parties informed.
• Organisation: Plan and prioritize effectively.
• Customer Awareness: Focus on satisfying internal and external customers.
• Attention to Detail: Ensure work and information are complete and precise.
• Problem Solving: Assess situations accurately and derive positive outcomes.