Scientist method validation Work, Jobs in Fleet, Ham (with Salaries)

Associate Scientist, Analytical
MedPharm —Guildford
- Full-time
- Computer literacy
- Laboratory experience
- Bachelor's degree
Quick apply
QC Scientist - Method Validation
Lonza —Slough
- Full-time
- Organisational skills
Scientist, Analytical
MedPharm —Guildford
- Full-time
- Computer literacy
- Laboratory experience
- Bachelor's degree
Quick apply
1d
Senior Scientist II
Mondelēz International —Reading
- Full-time
- Doctoral degree
- English
- No degree
- Employee assistance programme
- Employee discount
8d
Higher Scientist - Climate & Earth Observation (CEO)
NPL —Teddington
- Doctoral degree
- Master's degree
- Analysis skills
1d
BioAssay Scientist
Eurofins UK PSS —Slough
- Full-time
- Continuous improvement
- Organisational skills
- Computer skills
- Free parking
- Employee assistance programme
Quick apply
Head of Patient Science, Instrument Development & Thought Leadership
IQVIA —Reading
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Team management
- Work from home
Lab Automation Scientist
Lonza —Slough
- Full-time
- Doctoral degree
- Master's degree
- Scripting
BioAssay Project Management Scientist
Eurofins UK PSS —Slough
- Full-time
- Continuous improvement
- Mentoring
- Training & development
- Free parking
- Annual leave
Quick apply
12d
Project Manager
Mondelēz International —Reading
- Full-time
- Doctoral degree
- Computer literacy
- English
- Employee assistance programme
- Employee discount
7d
Senior Postdoctoral Scientist
Pirbright Institute —Pirbright
- £50,500 - £53,000 a year
- Full-time
- Doctoral degree
- Research
- Travel
- Free parking
- Annual leave
Quick apply
12d

Related jobs to explore

Based on your search for scientist method validation

Associate Scientist, Analytical
MedPharm —Guildford
This role requires strong technical and organizational skills, attention to detail, and a commitment to scientific excellence in a fast-paced, collaborative R&D…
Quick apply
QC Scientist - Method Validation
Lonza —Slough
Support troubleshooting activities and contribute to out-of-specification (OOS) and laboratory investigations. This is a fully site‑based role.

I want to receive the latest job alerts for scientist method validation in fleet, ham

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Associate Scientist, Analytical

MedPharm -
Guildford

Quick apply

Job details

Full-time

Qualifications

GLP
Analytical chemistry
Computer literacy
Laboratory experience
Internal department liaison
Microsoft Office Suite
Bachelor's degree
Continuous improvement
Organisational skills
Computer skills
Research & development
Communication skills
FDA regulations
Time management
Analytics
COSHH compliance

Full job description

General Information

Title: Associate Scientist

Department: Analytical

Site: Guildford

Reporting To: Team Leader

Position Summary
The Associate Scientist (Analytical) plays a key role in supporting research and development studies by performing analytical testing of pharmaceutical compound, drug substance and drug product. This role is integral to the development of new drug formulations, ensuring accurate data generation to guide formulation design and process development. Working under the supervision of team leaders and senior scientists, the associate scientist is responsible for executing analysis through HPLC and GC in compliance with internal protocols and industry standards. The position involves HPLC method development and optimisation to support early and late-stage pharmaceutical development. This role requires strong technical and organizational skills, attention to detail, and a commitment to scientific excellence in a fast-paced, collaborative R&D environment.

Essential Functions

Responsible for executing a variety of analytical techniques such as HPLC and GC to support the development of pharmaceutical drug products as well as assist in the day-to-day running of the laboratory in compliance with MedPharm’s QMS.
Performing pre-defined experiments according to internal standard operating procedures (SOP) (e.g. forced degradation of substance and product, saturated solubility, excipient compatibility and formulation stability).
Support analytical method development and validation in accordance with ICH and FDA guidelines.
Accurately document all experiments and results and have a good understanding and demonstration of good laboratory practice (GLP), data integrity and quality.
Analyze data using Empower and interpret results to support formulation development, stability studies and product release.
Take an active responsibility for your analytical work with respect to quality and compliance, particularly in the support of the analytical team.
To assist the progression of the study by collaborating with other departments, with oversight from your supervisor where appropriate. To attend meetings and contribute when appropriate.
To aid in the department’s method development and continuous improvement strategies
Adhere to Health and Safety and COSHH regulations and read relevant safety data sheets and risk assessments prior to undertaking work.
To maintain your training file (physical and MasterControl based) and to not use any equipment or handle any chemicals without following the appropriate health and safety guidance.
To undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment
To conduct yourself in concordance with the MedPharm Ethos, professionalism and confidentiality.

Key Relationships (examples: Depts or Individual positions that this position will be working closely with):

R&D Laboratory staff
Analytical Team Leaders
FD, PD and PT Study Managers
Project Management team
QC team
Quality Assurance team

Education and Experience

Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline.
Familiarity with common analytical equipment and instrumentation (e.g. analytical balance, pH meter, HPLC, GC)

Knowledge, Skills, and Abilities

Computer literate and knowledgeable in Microsoft Office Applications
Effective oral and written communication
Good observation skills and ability to document accurately
Strong ability to work in teams and collaboration
Good time management and organizational skills
Good knowledge and practical experience in analytical laboratory

Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.

Example:

Occasionally required to lift up to 20kg
Requires standing for extended periods
May be exposed to loud noise levels
May be exposed to hot or cold temperatures

Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.

8ROYQe5Ry1

Quick apply

Refine Your Search

scientist method validation jobs in fleet, ham

Associate Scientist, Analytical

QC Scientist - Method Validation

Scientist, Analytical

Senior Scientist II

Higher Scientist - Climate & Earth Observation (CEO)

BioAssay Scientist

Head of Patient Science, Instrument Development & Thought Leadership

Lab Automation Scientist

BioAssay Project Management Scientist

Project Manager

Senior Postdoctoral Scientist

Related jobs to explore

I want to receive the latest job alerts for scientist method validation in fleet, ham

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected