Pharmaceutical Work, Jobs in Newry, Dow (with Salaries)

Formulations Analyst
Norbrook Laboratories —Newry
- Full-time
- Laboratory experience
- Microsoft Office
- Quality control
- Free parking
- Annual leave
Quick apply
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Almac Group —Craigavon
- Full-time
- Bachelor's degree
- Communication skills
Formulation Development Group Leader
Almac Group —Craigavon
- Full-time
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Study Director (Process Validations)
Norbrook Laboratories —Newry
- Full-time
- Supervising experience
- Project management
- Free parking
- Health & wellbeing programme
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Production Technician - Graduate Opportunities
Almac Group —Craigavon
- Full-time
Technical Graduate Opportunities
Almac Group —Craigavon
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Marketing Associate – Digital Media
Almac Group —Craigavon
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Senior Crystallisation Process Development Chemist
Almac Group —Craigavon
- Full-time
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Sales Development Representative
EPAM Systems, Inc. —Newry
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- Customer service
- Employee assistance programme
- Referral programme
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Santen —Newcastle
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Maintenance Engineer
Almac Group —Craigavon
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Formulations Analyst

Norbrook Laboratories -
Newry

Quick apply

Job details

Permanent | Full-time

Benefits

Free parking
Annual leave
Company pension
Canteen
Employee assistance programme
Sick pay
On-site parking

Qualifications

Scientific research
Laboratory experience
Microsoft Office
Biochemistry
Quality control
Communication skills

Full job description

Job summary

Applications are invited for the position of Formulations Analyst, based within R&D Formulations, Pharmaceutical Development, reporting to the Section Head of Formulations Analytical.

The purpose of this position is to perform physicochemical evaluation and compositional analysis of Norbrook development and reference products in accordance to SOPs and relevant standards

Main Tasks/Activities

Development and optimisation of chemical and physical analytical methods to support early stage and late-stage formulation development of new and existing products.
Ensure developing trends and risks within projects are identified to allow timely investigation where necessary to help ensure product viability
Generate, interpret, and trend data for critical quality attributes (CQAs) to support formulation optimisation and decision making.
Maintain accurate records and prepare reports for both group and R&D management to include reverse engineering, pre-formulation, method validation, product specification justification and pharmaceutical development reports.
Develop an understanding and ownership of projects, ensuring developing trends and risks are identified to allow timely investigation where necessary to help ensure product viability.
Assist in the training of Laboratory personnel in analytical techniques and SOP compliance.
To carry out validation, calibration and cleaning of equipment as required.
To characterise reference standards.
To assist in the preparation of Standard Operating Procedures and Methods.
To ensure adequate stocks of consumables are available as required.
Maintain clean and safe working environment within the laboratories, following all COSHH and other Health and Safety requirements.
To carry out any miscellaneous investigations or other activities as requested by management.

Essential Criteria:
Applicants must therefore demonstrate the following essential criteria on their application form in order to be considered:

Third level qualification in Chemistry or a related subject.
Minimum 2 years' experience within a chemistry analytical laboratory including HPLC/UHPLC and Dissolution techniques.
Excellent oral and written communication skills.
Good organisation skills and the ability to prioritise and show flexibility to meet the demands of a busy laboratory.
Proficiency in use of Microsoft Office program suite.
Demonstrated ability to work well within a team.
Proactive approach towards problem solving.

Desirable Criteria:
Due to the nature of the role preference will be given to applicants demonstrating the following desirable criteria:

Previous experience assessing dissolution profiles (f2).
Previous experience of specification setting/justification.
Design and execution of product development studies according to regulatory guidance.
A good understanding of cGMP/GLP.
Experience in formulation development and stability studies.

Duration: Full Time, Permanent
Location: Newry

Additional Information:
This role will be based in a site that produces and handles penicillin, and as such, this role would not be suitable for those that have a penicillin allergy.

Benefits:
Free life assurance
Company pension scheme
Healthcare cash plan
32 days annual leave
Wedding leave
Company sick pay
Employee well-being initiatives
Employee assistance programme
On-site free parking
Subsidised canteen facilities
WeCare programme – supporting the local community
Employee perks scheme
Employee recognition scheme
Career development opportunities

To Apply Please forward your CV via the APPLY Now button below.

Benefits:

Canteen
Company pension
Free parking
On-site parking

Work Location: In person

Quick apply

Refine Your Search

pharmaceutical jobs in newry, dow

Formulations Analyst

Pharmaceutical Development - Graduate Opportunities

Formulation Development Group Leader

Study Director (Process Validations)

Production Technician - Graduate Opportunities

Technical Graduate Opportunities

Marketing Associate – Digital Media

Senior Crystallisation Process Development Chemist

Sales Development Representative

Ophthalmology Account Manager - Scotland & North East

Maintenance Engineer

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