Senior Analyst

TN United Kingdom; Loughborough; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading company in Pharma Services is seeking a qualified professional to join their team in Loughborough. The role involves analytical work to GMP standards, with opportunities for personal and professional development. Candidates should have significant experience in drug product development and method validation. An attractive benefits package is offered, including a competitive salary and annual bonus.

Benefits

Competitive Salary

Annual Bonus

Employer Pension Contributions

34 Days Paid Annual Leave

Healthcare Benefits

Qualifications

• Significant experience in GMP drug product development laboratory.
• Experience in developing/validating methods for drug products.

Responsibilities

• Monitor progress of analytical work to GMP requirements.
• Ensure project schedules are met efficiently and accurately.

Skills

Analytical Techniques

GMP Requirements

Method Development

Education

B.Sc. in Chemistry

M.Sc./PhD in Chemistry

Tools

Empower

LC-MS

Job description

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Hours: 37.5 hours per week. Flexible working hours. Monday to Friday.

Ref No: HRJOB10656

Business Unit: Pharma Services

Location: Loughborough, Leicestershire, UL

Open To: Internal and external candidates

The Role

Working as part of the Pharma Services team based in our Charnwood site in Loughborough, you will be responsible for carrying out and monitoring the progress of Analytical work to GMP requirements, to ensure that project schedules are met and that the work is carried out efficiently and accurately.

As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group.

· B.Sc. (or equivalent) in Chemistry or a Life Science subject with a significant chemistry component.

· Significant experience working in a GMP drug product development laboratory.

· Significant experience of analysing development drug products.

· Significant experience of developing/validating methods for development drug products using a variety of analytical techniques including Dissolution, HPLC.

· Significant Experience of Stability Testing for drug products including assay/related substances, dissolution analysis

(The following criteria may be applied if a large pool of applicants exist)

· M.Sc./PhD (or equivalent in a Chemistry or Life Science with a significant chemistry component

· Experience in supervising or line managing a team of analysts.

· Experience of using Empower chromatography data capture system

· Experience in the use of LC-MS systems

· Experience of GMP raw material testing for API, excipients and packaging components

· Experience of conducting cleaning validations and verifications.

Reward

For the successful candidate, we offer an attractive benefits package which includes a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more.

Closing Date: Sunday 1st June 2025 at 1700 hours

RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited, and no fee will be payable. Thank you for your cooperation