Laboratory Technician, QC Finished Products

Laboratory Technician, QC Finished Products, Brighton

Client:

Custom Pharma Services

Location:

Brighton, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

e0142528d072

Job Views:

3

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Full time MoulsecoombRole overview

Laboratory Technician, Quality Control (One Year Fixed-Term Contract)

We are now looking for an additional experienced Technician to join us to work within our Finished Products Team on a one year contract. The role involves carrying out hands-on analyses (including HPLC and various wet chemistry techniques) of finished products to ensure regulatory requirements for the product are met; supporting the Finished Products Team Manager to achieve the appropriate throughput of samples for testing; output of consistently accurate data and reports to meet quality standards through conformance with up-to-date procedures, methods, internal SOP’s, Health & Safety and current principles of GMP/GLP.

Please note: Applicants must have the right to work in the UK without requiring sponsorship, we do not hold a sponsorship licence.

Work abroad

Please note: This position is not intended to fulfil the requirements of a student placement program.

Strictly no agencies please.

About Custom Pharma Services (CPS)

Custom Pharma Services is located in Brighton, UK since 1979 and is a full-service contract development and manufacturing organisation (CDMO) providing services tailored to your needs, no matter how niche or complex. Custom covers the full spectrum of activities from development through commercial manufacturing for both clinical and commercial use. Specialising in Oral Solid Dosage forms with the ability to handle highly potent drugs and poorly bioavailable compounds Custom really is your one stop resource. With direct access to highly skilled experts offering a partnership approach Custom Pharma Services truly has a molecule first mentality, managing all projects with the end in mind. Custom Can!

Custom is an Investors in People Silver accredited workplace where teamwork and support is encouraged, and where every individual is valued and supported to achieve their full potential because if you can, then Custom Can!

As a QC Technician in our Finished Products team you will be:

Participating in the timely analysis of intermediate and finished products

Participating in the generation of and ensuring the authorisation and output of consistently accurate data and analytical reports through conformance with current principles of GMP/GLP. Ensuring equipment is properly maintained, and calibrated, taking personal responsibility for one or more groups of equipment

Ensuring the QC laboratories are well organised, reagents/ standards are available and controlled

Applying expertise and a systematic approach to problem solving

Participating in achievement of site KPI's by completion of QC and customer objectives, and focussing on tasks linked to overall site performance

Improve the adherence to customer quality requirements by applying principles of GMP /GLP

Proposing new ideas in order to improve performance within own area of responsibility

Use of HPLC systems, including basic troubleshooting

When required, supporting the Raw Materials, Development and Stability Teams within the Laboratory, and Goods-In material handling processes

We would like to hear from you if your background, experience, and skills include:

A degree in chemistry or other closely related science discipline

A chemistry background and previous experience in finished products and/or stability testing with solid dose finished products is preferable. Or other pharmaceutical medicinal products will also be considered

Previous experience within a QC or development environment in the pharmaceutical industry or similar GMP environment

HPLC experience

Working knowledge of GMP and GLP

A familiarity with laboratory equipment/ techniques/ procedures and documentation systems

The ability to plan and prioritise workload

Competence in Microsoft Word and Excel i.e., Basic level

Attention to detail

The ability to follow written procedures with accuracy and efficiency

Able to work effectively with minimum supervision in a team or alone

Good verbal and written communication skills

Adaptable and flexible to meet changing priorities

Understanding of UK, EU and other specific analytical regulations for the pharmaceutical industry would be a bonus.

Our benefits package includes:

Group personal pension scheme

Life assurance at twice annual salary

Health Plan with Simply Health including access to a GP or Counselling Services 24/7, money back on prescriptions, optical, dental and physiotherapy

Ride to work scheme

Subsidised Gym Membership

Discount Shopping Portal

Employee Referral Scheme bonus of £1,000

Values based awards

Successful candidates will be required to complete a basic disclosure check.

Department Laboratory Contract type Fixed Term Contract Hours 38.75 Salary £28,047.59 Benefits CompetitiveShare this job LinkedinTwitterFacebookEmail

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Created on 26/04/2025 by TN United Kingdom