Stability analyst Work, Jobs in Livingston, Wln (with Salaries)

QC Analyst
NextPharma —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Free parking
- Health & wellbeing programme
Quick apply
QC Stability Analyst
NextPharma —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Free parking
- Health & wellbeing programme
Quick apply
5d
QC Technician (Analytical)
Valneva —Livingston
- £28,000 - £32,000 a year
- Weekend availability
- Laboratory experience
- Quality control
- Employee assistance programme
- Gym membership
Quick apply
Specialist Quality Control
NextPharma GmbH —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Quality control
- Life insurance
5d
Senior Business Analyst
Version 1 —Edinburgh
- Full-time
- Hybrid work
- Agile
- Communication skills
- Life insurance
Quick apply
Financial Risk Analyst
X-Orsystem —Edinburgh
- £82,000 a year
- Full-time
- In-person
- Banking
- Sick pay
Quick apply
3d
QC Team Leader (Technical Support)
Piramal Healthcare UK Limited —Grangemouth
- Quality control
11d
Senior Finance Analyst
Aegon —Edinburgh
- £47,680 - £71,520 a year
- Full-time
- Hybrid work
- Presentation skills
- Accounting
- Budgeting
9d
Senior Appian Development Consultant
Valtech Group —Edinburgh
- Mentoring
- Communication skills
Senior Finance Analyst
Aegon UK —Edinburgh
- £47,680 - £71,520 a year
- Full-time
- Hybrid work
- Presentation skills
- Accounting
- Budgeting
9d

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QC Analyst
NextPharma —Livingston
Literacy and Numeracy:* Must be competent in writing reports both for internal use and for customers. Actively involved in performing analytical activities to…
Quick apply
QC Stability Analyst
NextPharma —Livingston
Literacy and Numeracy:* Must be competent in writing reports both for internal use and for customers. Actively involved in performing analytical activities for…
Quick apply
5d

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stability analyst jobs near livingston, wln

QC Analyst

NextPharma -
Livingston

Quick apply

Job details

Permanent | Full-time

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 Word
Report writing
GLP
Report generation
Analytical chemistry
Computer literacy
Quality control within general manufacturing industry
Microsoft Office Suite
Numeracy
Quality control
Pharmaceutical industry setting experience
Instrumentation calibration
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 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

stability analyst jobs in livingston, wln

QC Analyst

QC Stability Analyst

QC Technician (Analytical)

Specialist Quality Control

Senior Business Analyst

Financial Risk Analyst

QC Team Leader (Technical Support)

Senior Finance Analyst

Senior Appian Development Consultant

Senior Finance Analyst

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