Chemist Work, Jobs in Dalmeny, Edh (with Salaries)

QC Analyst
NextPharma —Livingston
- Full-time
- Microsoft Office
- Quality control
- In-person
- Free parking
- Health & wellbeing programme
Quick apply
1d
Scientist-Analytical Research & Development
Veranova L P —Edinburgh
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
- Annual leave
- Life insurance
Quick apply
Pharmaceutical Solid State and Crystallization Scientist
PhysChem Solutions Ltd —Penicuik
- £28,000 - £40,000 a year
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
Quick apply
14d
Specialist Analytical Development
NextPharma GmbH —Livingston
- Full-time
- Microsoft Office
- Analysis skills
- Continuous improvement
- Life insurance
12d
Scientist Formulation Development
NextPharma GmbH —Livingston
- Full-time
- Doctoral degree
- English
- Microsoft Office
MDI Analytical Chemist
Orbia Fluor & Energy Materials —Thornton
- Full-time
- Computer literacy
- Bachelor's degree
13d
Senior Analytical Scientist
Impact Solutions —Livingston
- £35,000 - £40,000 a year
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
- Free parking
Quick apply
Development Analyst (Experienced)
NextPharma —Livingston
- Full-time
- Microsoft Office
- Analysis skills
- Continuous improvement
- Free parking
- Health & wellbeing programme
Quick apply
Scientific Associate, Chromatographic Bioanalysis
Charles River Laboratories —Tranent
- £27,951.22 a year
- Full-time
- Sales
- Bachelor's degree
- Free parking
- Employee discount
Postdoctoral Research Associate
University of Edinburgh —Edinburgh
- Full-time
- Doctoral degree
- English
- Annual leave
- Employee discount
Research Associate in Nanoscale Electrodeposition for Gas Sensing
University of Edinburgh —Edinburgh
- Full-time
- Doctoral degree
- Engineering
- Laboratory experience
- Annual leave
- Employee discount
6d
Senior Development Scientist - Environmental & Heavy Metal Sensing
Integrated Graphene —Stirling
- £44,500 - £53,150 a year
- Full-time
- Doctoral degree
- Master's degree
- Relocation assistance
- Annual leave
Quick apply
7d
Chemistry Analyst
Eurofins UK —Livingston
- Full-time
- Communication skills
Quick apply
11d

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QC Analyst

NextPharma -
Livingston

Quick apply

Job details

Permanent | Full-time
1 day ago

Benefits

Free parking
Health & wellbeing programme
Cycle to work scheme
Company pension
Company events
Private medical insurance
Life insurance
Referral programme
Sick pay
On-site parking

Qualifications

Microsoft Office
Quality control
Communication skills
FDA regulations

Full job description

NextPharma is a leading European pharmaceutical CDMO focused on attractive technology niches.

Since its foundation in 1989, the Livingston site has evolved into a global player in the development and application of both traditional and novel drug encapsulation technologies that are supported by modern and commercial scale manufacturing facilities. .

Our Vision:

Our vision is to be the leading and most trusted, reliable and innovative Europe-based CDMO by upholding the highest industry standards and exceeding customer expectations, while driving strong, sustainable growth for the company.

This role reports to the Quality Control Team Leader and will primarily be responsible for the conducting analytical activities, QC testing and release of materials, packaging components and finished products. 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.

Job Purpose:

To support the production of both development and market finished products under GMP conditions in all areas of quality control and calibration.

Key responsibilities and accountabilities:

1. Work as part of a team alongside Production and other analytical departments including development and stability.

2. Actively involved in performing analytical activities to determine fitness for purpose of starting materials, intermediate and finished products

3. Technically competent in analytical activities (e.g., pharmacopeial wet chemistry, HPLC, GC, Dissolution) for QC testing of raw materials, packaging components and finished products. All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia

4. Perform sampling of starting materials, packaging components and finished products

5. Perform cleaning verification analysis to assure suitability of Production equipment for subsequent use

6. Support calibration of key analytical equipment and measuring devices used in or on production equipment

7. Comply with company health and safety procedures.

Personality:

Results oriented with a positive outlook and clear focus on high quality output: Solid planning and organizational ability; Reliable, tolerant, and dependable: Comfortable dealing with senior managers and customers: Enjoy working in a fast, stimulating environment. 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.

Specific Job Skills:

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

· Skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and wet chemistry techniques

· Able to communicate well with others, both laboratory and non-laboratory based

· Able to work with minimal supervision.

· Good understanding of quality control, SOP and GMP adherence

Desired:

· Have a broad knowledge with and experience of working within a cGMP/GLP environment.

· Experience of working within a pharmaceutical or biotechnology industry

· Ability to work to key regulatory and compliance requirements

· Experience of quality control within a pharmaceutical environment

· Experience of Chromeleon software

· Experience of data reporting and checking data within a QC environment

· Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.

Computer skills: Must be competent in the use of MS Office, particularly Excel and Word,
e-mail and internet. Previous use of chromatographic acquisition software is desired but not essential.

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.

Remuneration Package:

Basic Salary: £DOE

Private Medical Insurance

Health Cash Plan

Contributory pension scheme

Please note: Only candidates with continuing Right to Work in the UK will be considered.

NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.

Benefits:

Company events
Cycle to work scheme
Free parking
Health & wellbeing programme
Life insurance
On-site parking
Private medical insurance
Referral programme
Sick pay

Work Location: In person

Quick apply

Refine Your Search

chemist jobs in dalmeny, edh

QC Analyst

Scientist-Analytical Research & Development

Pharmaceutical Solid State and Crystallization Scientist

Specialist Analytical Development

Scientist Formulation Development

MDI Analytical Chemist

Senior Analytical Scientist

Development Analyst (Experienced)

Scientific Associate, Chromatographic Bioanalysis

Postdoctoral Research Associate

Research Associate in Nanoscale Electrodeposition for Gas Sensing

Senior Development Scientist - Environmental & Heavy Metal Sensing

Chemistry Analyst

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