Research associate Work, Jobs in Tongham, Sry (with Salaries)

Associate Scientist, Analytical
MedPharm —Guildford
- Full-time
- Computer literacy
- Laboratory experience
- Microsoft Office
Quick apply
6d
Research Associate
Kingston University —Kingston upon Thames
- £39,407 - £43,835 a year
- Call to connect
- Doctoral degree
- Master's degree
- University
12d
Assistant Forensic technician
University of Surrey —Guildford
- £14,016 - £16,040 a year
- Part-time
- Hybrid work
- University
- Relocation assistance
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
6d
Postdoctoral Research Associate (PDRA)
Kew Gardens —Kew Gardens
- £39,243 - £42,153 a year
- Full-time
- Remote
- Doctoral degree
- Presentation skills
- Scripting
- Annual leave
- Employee assistance programme
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
9d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
12d
Senior Study Start Up Associate
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
8d
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- University
9d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- No degree
- Travel
1d
Associate Security & Privacy Researcher
NPL —Teddington
- Java
- Analysis skills
- C++
Associate Ecologist/Associate Director
AtkinsRéalis —Epsom
- Full-time
- Hybrid work
- Project management
- IT
CRA II, client-dedicated (fixed-term)
Fortrea —Maidenhead
- Full-time
- Travel
- Organisational skills
- Communication skills
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
9d
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Principal Biostatistician
Ergomed —Guildford
- Full-time
- Remote
- English
- Microsoft Office
- Master's degree
Quick apply
7h
Associate Director - Ecology
AECOM —Basingstoke
- Full-time
- Hybrid work

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research associate jobs near tongham, sry

Associate Scientist, Analytical

MedPharm -
Guildford

Quick apply

Job details

Full-time
6 days ago

Qualifications

Computer literacy
Laboratory experience
Microsoft Office
Quality assurance
Bachelor's degree
Organisational skills
Communication skills
FDA regulations
Time management

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.

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research associate jobs in tongham, sry

Associate Scientist, Analytical