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- Tasks: Conduct analytical testing on therapeutic proteins to ensure quality and stability.
- Company: Join a leading global biopharmaceutical company focused on innovative healthcare solutions.
- Benefits: Enjoy a competitive salary, supportive team environment, and opportunities for professional growth.
- Why this job: Kickstart your career in biochemistry with hands-on experience in a dynamic lab setting.
- Qualifications: Bachelor's/Master's in Biochemistry or Chemistry; 1-2 years industry experience required.
- Other info: This role is perfect for recent graduates eager to make an impact in the biopharmaceutical field.
This is a great opportunity for a graduate in a biochemistry related degree looking for their first role in the industry. 1-2 years industry experience is required for this role.
To perform analytical testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines.
Key Responsibilities will include:
- Performs experimental work independently in accordance with SOPs on a variety of sample types e.g drug substance and drug product release and stability samples, in-process samples.
- Performs work in a safe, compliant manner, ensuring training profile is maintained and up to date at all times.
- Plans and completes assigned tasks within the required timeframe and escalates any issues/delays to the Group Leader and/or scientific lead as appropriate.
- Liaise with reviewers and study directors to close out technical review of assays.
- Interpret data against specifications and identify trends within data.
- Support, as needed, with the timely completion of investigations, deviations, CAPAs and change controls.
- Actively contributes to QC department general lab housekeeping, ensuring the laboratory is adequately stocked with reagents and consumables as needed and may support with the monitoring and maintenance of equipment e.g. IMS.
- Work collaboratively in a team to ensure business, regulatory and customer needs are met.
Candidate Requirements:
- Bachelors/Masters in Biochemistry or Chemistry.
- 1-2 year experience in the industry is essential.
- GMP experience is essential.
- Experience in Protein Biochemistry and Monoclonal Antibodies would be desirable.
- Experience with HPLC or ELISA would be desirable.
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Technologist
✨Tip Number 1
Make sure to brush up on your knowledge of HPLC and ELISA techniques, as these are specifically mentioned in the job description. Being able to discuss your hands-on experience with these methods during an interview will show that you're well-prepared and knowledgeable.
✨Tip Number 2
Familiarise yourself with GMP guidelines and how they apply to quality control in biopharmaceuticals. Understanding these regulations will not only help you in the role but also demonstrate your commitment to compliance during the interview process.
✨Tip Number 3
Network with professionals in the biochemistry field, especially those who work in QC roles. Engaging with industry contacts can provide insights into the company culture and expectations, which can be invaluable when preparing for interviews.
✨Tip Number 4
Prepare to discuss your problem-solving skills, particularly in relation to investigations and deviations. Be ready to share examples from your past experiences where you successfully identified trends or resolved issues, as this is a key responsibility of the role.
We think you need these skills to ace QC Technologist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your biochemistry or chemistry degree and any relevant experience, especially in GMP environments. Include specific examples of analytical techniques you've used, such as HPLC or ELISA.
Craft a Strong Cover Letter: Write a cover letter that connects your academic background and industry experience to the responsibilities of the QC Technologist role. Emphasise your familiarity with quality control processes and your ability to work safely and compliantly.
Highlight Relevant Skills: In your application, clearly outline your skills related to analytical testing and data interpretation. Mention any experience with therapeutic proteins and your ability to work collaboratively in a team setting.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A polished application reflects your attention to detail, which is crucial in a QC role.
How to prepare for a job interview at SRG
✨Know Your Techniques
Make sure you brush up on your knowledge of analytical techniques like HPLC, electrophoresis, and spectrophotometry. Be prepared to discuss how you've used these methods in your previous experience or during your studies.
✨Understand GMP Guidelines
Since GMP experience is essential for this role, ensure you understand the principles of Good Manufacturing Practice. Be ready to explain how you have adhered to these guidelines in past roles or projects.
✨Showcase Your Problem-Solving Skills
The role involves interpreting data and identifying trends, so be prepared to discuss specific examples where you've successfully tackled challenges or resolved issues in a lab setting.
✨Emphasise Team Collaboration
This position requires working collaboratively within a team. Think of examples from your past experiences where you contributed to a team project, highlighting your communication skills and ability to work towards common goals.
