Senior quality analyst Work, Jobs in Newbridge, Edh (with Salaries)

QC Stability Analyst
NextPharma —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Free parking
- Health & wellbeing programme
Quick apply
10d
Specialist Quality Control
NextPharma GmbH —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Life insurance
9d
Senior Analyst
Eurofins UK BioPharma Services —Livingston
- Full-time
- Continuous improvement
- Communication skills
- Free parking
- Employee assistance programme
Quick apply
14d
HR Data and Reporting Analyst
The Progeny Group Limited —Edinburgh
- Hybrid work
- Data analysis skills
- Analysis skills
Quick apply
Programme Test Manager
Aegon —Edinburgh
- £52,720 - £79,080 a year
- Full-time
- Hybrid work
- Continuous improvement
- Team management
- Financial services
8d
Senior Business Analyst
University of Stirling —Stirling
- Full-time
- Analysis skills
- University
- Continuous improvement
12d
Programme Test Manager
Aegon UK —Edinburgh
- £52,720 - £79,080 a year
- Full-time
- Hybrid work
- Continuous improvement
- Team management
- Financial services
8d
Onsite Senior Technical Analyst, IT Infrastructure Services, Edinburgh
Deloitte —Edinburgh
- Hybrid work
- In-person
- Communication skills
Senior Lead Analyst
Royal London —Edinburgh
- Analysis skills
- Mentoring
- Training & development
- Annual leave
7d
Senior Test Engineer
Companies House —Edinburgh
- £41,509 - £52,509 a year
- Full-time
- Presentation skills
- Travel
- Leadership
- Annual leave
9d
ERP Business Analyst
MacTaggart Scott —Loanhead
- Full-time
- ERP systems
- Continuous improvement
- In-person
- Free parking
- Annual leave
Quick apply
Head of Prism Operations
Clearwater Analytics, LLC —Edinburgh
- £100,000 - £140,000 a year
- Computer Science
- Engineering
- Bachelor's degree
- Annual leave
Quick apply
2d
Senior Analyst, Project Administration Support, Asset Pricing Team, Audit and Assurance – 12 month FTC
Deloitte —Edinburgh
- Hybrid work
- No experience needed
- Communication skills
- Time management
Prism Team Lead
Clearwater Analytics, LLC —Edinburgh
- Computer literacy
- Writing skills
- SQL
Quick apply
13h
Cyber Security Business & Reporting Analyst
Computershare —Edinburgh
- Full-time
- Analysis skills
- Communication skills
- Work from home
Senior Infrastructure Engineer (Database Development)
Companies House —Edinburgh
- £41,509 - £52,509 a year
- Full-time
- Presentation skills
- Annual leave
9d
Senior Service Desk Analyst
Lane Clark & Peacock —Edinburgh
- Hybrid work
- Computer Science
- Windows
- Bachelor's degree
- Annual leave
- Employee discount
6d
Senior Business Analyst
Version 1 —Edinburgh
- Full-time
- Hybrid work
- Agile
- Communication skills
- Life insurance
Quick apply
BPA Manager (12 Months FTC)
Intergen —Edinburgh
- £68,000 - £72,000 a year
- Hybrid work
- Analysis skills
- In-person
- Sick pay
QC Team Leader (Technical Support)
Piramal Healthcare UK Limited —Grangemouth
- Quality control

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QC Stability Analyst

NextPharma -
Livingston

Quick apply

Job details

Permanent | Full-time
10 days ago

Benefits

Free parking
Health & wellbeing programme
Company pension
Company events
Private medical insurance
Paid volunteer time
Life insurance
Referral programme
Sick pay
On-site parking

Qualifications

Microsoft Word
Report writing
GLP
Report generation
Analytical chemistry
Computer literacy
Microsoft Office Suite
Numeracy
Quality control
Pharmaceutical industry setting experience
Communication skills
FDA regulations
Analytics

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 Stability Team Leader and will primarily be responsible for the conducting of stability analytical activitiesfor technical, clinical. and commercial products. There may also be a support function for QC, micro and analytical development departments. 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 on-going stability program for commercial, clinical and technical products. In addition support of quality control testing of both development and market finished products under GMP conditions

Key responsibilities and accountabilities:

1. Work as part of a team alongside quality control and micro departments

2. Actively involved in performing analytical activities for stability analysis of drug products

3. Must be technically competent in analytical activities (e.g. pharmacopoeail wet chemistry, HPLC, GC, Dissolution, KF) for stability testing of finished products. All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia

4. Writing of stability summaries, protocols and reports

5. Performing set down of new stability studies, receipt of stability samples being returned from storage facility and disposal of samples following reporting of analysis

6. Checking of data for stability, QC and micro departments

7. Ordering of lab supplies to ensure continued availability of materials for timely analysis

8. Comply with company health and safety procedures.

Person Profile: Quality Control Analyst (Stability)

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 is equally comfortable working independently.

Personal Situation

Flexible and able to work extended hours when required.

Must be eliglble to work in the UK.

Specific Job Skills:

Required:

· Relevant qualification, HNC/HND/Science Degree or Equivalent

· An understanding of drug development and stability processes

· Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards

· Must be skilled in analytical techniques eg HPLC, Dissolution, Gas Chromatography, KF 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.

· 2-3 years experience of working within a pharmaceutical or biotechnology industry

· Ability to work to key regulatory and compliance requirements

· Experience of quality control/Stability 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

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.

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
Company pension
Free parking
Health & wellbeing programme
Life insurance
On-site parking
Paid volunteer time
Private medical insurance
Referral programme
Sick pay

Experience:

HPLC: 1 year (required)

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

senior quality analyst jobs in newbridge, edh

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