Laboratory Technician, Quality Control

TieTalent; Brighton; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player is seeking a Laboratory Technician for a one-year fixed-term contract in Brighton. This role involves hands-on analysis of finished products, utilizing HPLC and wet chemistry techniques to ensure compliance with regulatory standards. You will play a vital role in supporting the Finished Products Team to achieve efficient sample throughput and deliver accurate data. Join a collaborative environment that values teamwork and individual potential, and contribute to quality control in a dynamic pharmaceutical setting.

Benefits

Pension Scheme

Life Assurance

Health Plan

Ride-to-Work Scheme

Subsidized Gym

Discount Shopping

Employee Referral Bonus

Values-Based Awards

Qualifications

• Degree in chemistry or related science discipline required.
• Experience in finished products and/or stability testing preferred.

Responsibilities

• Participate in the analysis of intermediate and finished products.
• Generate and ensure accuracy of analytical data and reports.
• Maintain and calibrate laboratory equipment.

Skills

HPLC

GMP

GLP

Analytical Skills

Problem-Solving

Communication Skills

Attention to Detail

Microsoft Word

Microsoft Excel

Education

Degree in Chemistry

Tools

Laboratory Equipment

Job description

About

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

We are seeking an experienced Technician to join our Finished Products Team on a one-year contract. The role involves hands-on analysis of finished products, including HPLC and wet chemistry techniques, to ensure compliance with regulatory standards. You will support the Team Manager to achieve efficient sample throughput, deliver accurate data and reports, and adhere to quality standards, SOPs, Health & Safety, and GMP/GLP principles.

About Custom Pharma Services (CPS)

Located in Brighton, UK, since 1979, Custom Pharma Services is a full-service contract development and manufacturing organisation (CDMO). We provide tailored services from development through commercial manufacturing, specializing in Oral Solid Dosage forms, handling highly potent drugs, and poorly bioavailable compounds. We pride ourselves on a molecule-first approach, working with highly skilled experts to manage projects with end goals in mind. Custom Pharma Services is an Investors in People Silver accredited workplace that values teamwork, support, and individual potential.

Role Responsibilities

1. Participate in the timely analysis of intermediate and finished products.
2. Generate and ensure the authorization and accuracy of analytical data and reports, conforming to GMP/GLP principles.
3. Maintain and calibrate equipment, taking responsibility for specific groups of equipment.
4. Organize laboratory resources, reagents, and standards.
5. Apply systematic problem-solving skills.
6. Contribute to site KPIs by completing QC and customer objectives.
7. Enhance compliance with customer quality requirements through GMP/GLP principles.
8. Propose ideas to improve area performance.
9. Operate HPLC systems, including troubleshooting.
10. Support other teams like Raw Materials, Development, and Stability, as needed.

Candidate Requirements

• Degree in chemistry or related science discipline.
• Experience in finished products and/or stability testing, preferably with solid dose products.
• Background in QC or development within the pharmaceutical GMP environment.
• HPLC experience.
• Knowledge of GMP and GLP.
• Familiarity with laboratory equipment, techniques, and documentation.
• Ability to plan, prioritize, and work independently or in a team.
• Proficiency in Microsoft Word and Excel.
• Attention to detail and accuracy in following procedures.
• Effective communication skills.
• Adaptability to changing priorities.
• Understanding of UK, EU, and other analytical regulations is a plus.

Benefits

Our benefits include pension scheme, life assurance, health plan, ride-to-work scheme, subsidized gym, discount shopping, employee referral bonus, and values-based awards.

Additional Information

Applicants must have the right to work in the UK without sponsorship. Successful candidates will undergo a basic disclosure check. This position is not a student placement. No agency applications accepted.

Location: Moulscoomb, Brighton
Contract: 1 Year FTC
Hours: Full-time, 38.75 hours/week
Salary: £(phone number removed)