Undergraduate Process Development Scientist at SGS

, Scotland, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

07 Jun, 26

Salary

24789.0

Posted On

09 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Development, Scale-Up, GMP, Formulation Development, Validation, Clinical Trial Supply, Troubleshooting, Scientific Reasoning, Teamwork, Data Analysis, Accurate Weighing, Process Calculations, Written Communication, Verbal Communication, Data Integrity

Industry

Professional Services

Description

Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognised as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability. Health & Nutrition Life Science- SGS’s Life Sciences services support the pharmaceutical, biotech, and healthcare sectors with expert testing, clinical research, auditing, and certification—ensuring product safety, quality, and regulatory compliance from development to market Job Description Role: Undergraduate Process Development Scientist Job Type: 12 months temporary contract Location: Deeside Hours: 37.5 hours, Monday to Friday Salary: £21,500- £24,789 (salary dependent on minimum wage for age group) Industry: Life Science Join SGS Quay Pharma as an Industrial Placement Process Development Scientist and gain hands‑on experience supporting pharmaceutical manufacturing process development, scale‑up, and clinical supply activities within a GMP‑focused environment. Carrying out experimental and process development work, documenting all activities to high GMP standards. Supporting the development, transfer, and scale‑up of manufacturing processes for liquids, solid dose, and live‑biotherapeutic products. Using a range of processing equipment to build robust, scalable pharmaceutical processes. Assisting with formulation development, production manufacturing, validation activities, and clinical trial supply—including packing and labelling support. Helping troubleshoot process and equipment challenges using scientific reasoning and teamwork. Communicating progress and working collaboratively to meet project timelines. Qualifications GCSE English Language (4/C+) and Maths (4/C+). Enrolled on a science degree (e.g., Chemistry, Pharmaceutical Sciences, Chemical/Biochemical Engineering or related), with completed laboratory modules. Essential Skills & Knowledge Understanding of pharmaceutical process development principles, including scale‑up and basic validation concepts. Confident with practical lab and pilot‑scale techniques: solution prep, accurate weighing, process calculations. Developing problem‑solving skills with enthusiasm for learning new process equipment and technologies. Competent in MS Excel for data analysis and process monitoring. Clear and confident written and verbal communicator with a strong commitment to quality and data integrity. Additional Information At SGS, we believe in rewarding our employees for their hard work and commitment. As part of our team, you would be eligible for: Generous Annual Leave allowance, plus bank holidays Retailer Discounts Health & Wellbeing initiatives Discounted Gym Membership SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, colour, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. APPLY NOW for full consideration, if you are selected for an interview, or further consideration, we will be in touch with you directly.

Responsibilities

The role involves supporting pharmaceutical manufacturing process development, scale-up, and clinical supply activities by carrying out experimental work and documenting all activities to high GMP standards. This includes supporting the development and transfer of manufacturing processes for various product forms and assisting with validation and clinical trial supply tasks.