Bioassay Scientist

Piramal Pharma Ltd


Date: 7 hours ago
City: Falkirk, Scotland
Contract type: Full time
Job Description

Key Roles/Responsibilities: Roles/Responsibilities:

Departmental Operations

  • Perform assigned work as agreed with the project lead and/or Analytical Development Manager. Ensure efficient use of time to complete the assigned objectives
  • Maintain laboratory areas, ensuring procedures are complied with to meet client, regulatory GMP and safety requirements.
  • Provide training and troubleshooting support to production and stability Quality Control groups.
  • Provide QC support (if required.)
  • Engage in specified compliance and improvement projects.
  • Provide cover for other Analytical Development Scientists as required.
  • 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.
  • Identify opportunities for improved methods of working to enhance efficiency, cost control and safety/GMP performance.
  • Support training of new members of staff to the company / department.

Project Delivery

  • Responsible for ensuring that assigned project deliverables are fully completed on time.
  • Lead aspects of projects as appropriate and in agreement with the Analytical Development Manager.
  • Plan and carry out work, as agreed with the project lead, to ensure effective project progression in line with customer requirements.
  • Support method development, technical transfer, qualification and validation activities.
  • Provide analytical development project support, ensuring compliant introduction into QC, production and stability groups – have involvement in decisions on scheduling of development, technical transfer and validation in conjunction with other technical staff.
  • Workload planning with other staff to ensure required timelines are met.
  • Provide QC support if required.
  • Client communication as required, in a professional manner.

Quality

  • Ensure timely close out of deviations, change controls and commitment tracking.
  • Uphold cGMP principles and ESH standards, continually seek opportunities to improve and enhance standards, and encourage other staff to do likewise.
  • Record all laboratory work in standard official notebooks and compile results and observations for incorporation into technical reports. Adhere to the relevant procedures.
  • Follow all appropriate protocols and procedures as required for the work undertaken.
  • Ensure accuracy of raw data and analytical interpretations

Key Competencies

  • Teamwork -As a team member, the ability and desire to work cooperatively with others on a team
  • Communication - The ability to ensure that information is passed on to others who should be kept informed.
  • Organisation – The ability to efficiently plan and prioritise across a range of timeframes, making efficient use of time.
  • Customer Awareness - The ability to demonstrate concern for satisfying one’s external and/or internal customers.
  • Attention to Detail - Ensuring that one’s own and others’ work and information are complete and accurate
  • Problem Solving – The ability to accurately assess a situation and derive a positive outcome.

Qualifications

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.
Post a CV

See more jobs in Falkirk