Specialist Analytical Development

NextPharma; City of Edinburgh; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Edinburgh is seeking a Development Analyst to conduct analysis and development in a GMP regulated environment. The candidate will play a key role in method development and validation, requiring strong analytical skills and experience in HPLC and Gas Chromatography. This role offers a competitive salary and benefits package.

Benefits

Private Medical Insurance

Health Cash Plan

Contributory pension scheme

Life Insurance

Qualifications

• Relevant qualification in a science-related field.
• Demonstrated technical competence in analytical activities.
• Experience with GMP/GLP environments.

Responsibilities

• Conduct analysis to support formulation development.
• Perform method development, validation, and transfer.
• Write development and validation protocols and reports.

Skills

HPLC

Gas Chromatography

Dissolution

Analytical Techniques

Problem Solving

Education

HNC/HND/Science Degree or Equivalent

Tools

Chromeleon software

MS Office

Job description

Overview

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,500 employees in Germany, France, Finland, Norway and the UK. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.

Job Purpose

Development analyst: To conduct analysis, technical stability studies, development, validation and transfer of analytical methods. The role will be responsible for providing technical expertise at both a theoretical and practical level. The ideal candidate will therefore have a pharmaceutical analysis background and have gained experience within a cGMP, FDA and MHRA regulated environment.

Key Responsibilities And Accountabilities

• Work as part of a team alongside other analytical departments.
• Actively involved in performing analytical activities to determine fitness for purpose of finished products.
• Conduct analysis to support formulation development.
• Perform method development, validation and transfer analysis of analytical methods for Liquid Fill hard capsules.
• Technically competent in analytical activities (e.g., method development and validation, HPLC, GC, Karl Fischer and Dissolution) with validation activities performed under current cGMP and ICH Q2.
• Writing of development and validation protocols and reports.
• Checking of analytical data.
• Supporting good internal and external relationships and communication.
• Comply with company health and safety procedures.

Person Profile: Development Analyst

Personality

• Results oriented with a positive outlook and clear focus on high quality output.
• Solid planning and organizational ability; reliable, tolerant and dependable.
• Enjoy working in a stimulating environment; comfortable dealing with peers and customers.
• Goal-oriented: able to work under pressure and meet deadlines; excellent communication/presentation skills.
• Able to get on with others and be a team player, but equally comfortable working independently.

Personal Situation

Flexible and able to work extended hours when required.

Required

• Relevant qualification, HNC/HND/Science Degree or Equivalent.
• An understanding of drug development and manufacturing processes.
• Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards.
• Must be skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and Karl Fischer techniques.
• Experience of the technical and practical skills involved in stability studies, method development, transfer and validation.
• Able to communicate well with others, both laboratory and non-laboratory based.
• Able to work with minimal supervision.
• Good understanding of working within cGMP/GLP environment.

Desired

• Experience of working within a fast paced pharmaceutical or biotechnology industry.
• Minimum 3 years previous relevant experience in similar environment.
• Ability to work to key regulatory and compliance requirements.
• Experience of Chromeleon software.
• Experience of chemical analysis within a pharmaceutical environment (with formulations of drug products for pre-clinical and clinical trials).
• Experience of data reporting and data checking to GMP standards.
• Able to work with minimal supervision and provide guidance to junior analytical analysts.
• Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.
• Able to communicate well via written media with specific emphasis on report writing.

Computer Skills

Must be competent in the use of MS Office, particularly Excel and Word, e-mail and internet.

Literacy and Numeracy

Must be competent in writing reports both for internal use and for customers. Must be competent in the interpretation of analytical data.

Business Presentation Skills

Must be an excellent face-to-face and telephone communicator.

Notes

Please note – we are unable to offer Visa Sponsorship for this role.

Remuneration Package

• Basic Salary: £DOE
• Private Medical Insurance
• Health Cash Plan
• Contributory pension scheme
• Life Insurance