Enable job alerts via email!

Analytical Chemist

Kindeva Drug Delivery

Loughborough

On-site

GBP 30,000 - 40,000

Full time

3 days ago
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Start fresh or import an existing resume

Job summary

A leading company in the pharmaceutical sector is seeking a professional for their Loughborough site to join their team for the testing and development of inhalation products. The role requires a degree in a relevant scientific discipline and experience in pharmaceutical testing, focusing on compliance with GMP regulations and working collaboratively in a dynamic environment.

Benefits

Attractive compensation package
Company pension scheme (up to 10% employer contribution)
25 days holiday per year
Company sick pay
Employee Assistance Program
Flexible working hours
Free on-site parking
Cycle to work scheme
Discount and cashback at many retailers
Employee referral scheme

Qualifications

  • Experience in pharmaceutical product testing is preferable.
  • Method development and validation of analytical methods is desirable.
  • Good understanding of GMP and GLP.

Responsibilities

  • Carry out analytical testing compliant with GMP regulations.
  • Produce laboratory investigation reports.
  • Input to protocol design for robust data outcomes.

Skills

Understanding of GMP
Analytical Chemistry
Testing of pressurised metered dose inhalers

Education

Degree in relevant scientific discipline

Tools

HPLC
GC
MS
UPLC
UV

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

Role Overview

The Kindeva Drug Delivery Ltd. site in Loughborough manufactures and packages pharmaceutical and medical products in various forms.

This role will be working as part of a team responsible for the testing and development of new inhalation pharmaceutical products as part of a successful CDMO organisation.

Key Responsibilities Include, But Are Not Limited To

  • Carry out analytical testing compliant with GMP regulations, delivering to plan on time and in full.
  • Input to protocol design to deliver robust data and outcomes whilst working in a fast, flexible environment, with a strong focus on right first time.
  • Produce laboratory investigation reports (preliminary) and/or quality incident reports.
  • Represent the department as and when required. Including the potential to interact with internal and external customers and regulators.
  • Promote a “safety first” culture and environment.
  • Raise and report any safety incident as required.
  • Complete Corrective Action Preventative Action (CAPA) closures on time in full.

Skills & Experience

  • Experience in pharmaceutical product testing is preferable.
  • Testing of pressurised metered dose inhalers is preferable.
  • Degree qualified (or higher) in a relevant scientific discipline with practical laboratory elements.
  • Method development and validation of analytical methods is desirable.
  • Good understanding of GMP and GLP.
  • Knowledge of Analytical Chemistry and its practical application.
  • Working knowledge of Analytical instrumentation, preferably GC, MS, UPLC and UV. HPLC knowledge is essential.
  • Understanding of basic statistics and experimental design is desirable.
  • Computer literate, familiar with Microsoft Word and Excel.

Key Capabilities

  • Good organisational, interpersonal, and time management skills.
  • Enthusiastic, flexible, conscientious and proactive in approach.
  • To work efficiently with supervision or unsupervised as required.
  • Take a positive approach to own training and development.
  • Good decision-making and problem-solving skills.
  • Strong verbal and numerical aptitude skills.
  • Good communication skills.
  • Strong team player with the ability to work independently.

What We Offer

  • Attractive compensation package.
  • Company pension scheme (up to 10% employer contribution).
  • 25 days holiday per year (plus bank holidays) plus service days after 5 years
  • Company sick pay.
  • Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family.
  • Life assurance of four times life cover salary.
  • Flexible working hours.
  • Wellness programmes.
  • Employee recognition program.
  • Employee development.
  • Free on-site parking.
  • Discount and cashback at many retailers.
  • Cycle to work scheme.
  • Flu vaccinations.
  • Employee referral scheme.

Additional Information

Working Hours: 37.5hrs per week

Location: Charnwood Campus, Loughborough

All applicants must be eligible to work in the UK.

We believe our people make the difference at Kindeva Drug Delivery, we look for skilled, passionate, and driven professionals to come and work with us to help us excel in manufacturing technologies and processes, which bring lifesaving products to patients worldwide.

Apply Now

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.