Senior Manufacturing Scientist - Aseptic
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Position Overview & Specifications
Senior Manufacturing Scientist - Aspetic
Company Overview
Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients.
As a growing and successful business, we employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA.
Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.
The Role
Quotient Sciences are expanding rapidly, with a clear commitment to drug substance development and manufacture and have recently announced a $8m investment in a new kilo lab facility which will be fully operational in 2022.
Due to increasing demand and investment in new isolator technologies, we are currently recruiting for a Senior Manufacturing Scientist to dispense, manufacture and package clinical products in accordance with GMP requirements and company procedures.
This role will be focussed on aseptic manufacturing so knowledge of isolator technology, good aseptic technique and operation within cleanrooms would be a distinct advantage.
The Candidate
The key tasks and responsibilities of the position are:
- Help coordinate and participate in the manufacture and packaging of oral and intravenous clinical products, with a focus on aseptic manufacturing. Prepare and complete documentation associated with the manufacture and supply of clinical products.
- Dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use and maintain GMP stocks as required.
- Participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment. Help manage the manufacturing equipment maintenance, calibration and servicing programme.
- Ensure appropriate communication of manufacturing activities to the Project Lead
- Help plan and conduct process development studies or the manufacture of non-clinical batches in the development of clinical formulations or the transfer of developed formulations into the GMP facility.
- Participate in the upkeep of the GMP material inventory including ordering, goods receipt, storage and stock control, liaising as appropriate with the Quality Control and microbiology teams and Purchasing officer.
- Line manage a small team of Manufacturing Scientists.
- Work with due regards to health and safety of self and others.
- Work flexibly across the site to meet business needs.
The successful candidate will have
- BSc of equivalent in a relevant scientific discipline.
- Two to three years experience in the manufacture of clinical formulations and working in a GMP regulated facility/manner and some knowledge of the drug development process.
- Good written and oral communication skills.
- Flexible approach to new work challenges.
Other skills and experience required:
- Good written/oral communication skills
- A high level of personal integrity and commitment
- Flexible approach to new work challenges
Company benefits:
In return, you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.
Our commitment to Diversity & Inclusion
Quotient Sciences business are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient family by remaining committed to the development of our culture, equality, mindset, diversity & inclusions in the workplace.
As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. All applicants welcome.
Candidate Selection & Onboarding Process
Application & Resume Screening
Submit your tailored CV/Resume directly to the talent acquisition portal.
Technical & Competency Interviews
Virtual interviews with the hiring manager and multidisciplinary team.
Formal Offer & Benefits Negotiation
Written agreement outlining compensation, equity, retirement vesting, and relocation allowances.
Onboarding & Corporate Integration
Equipment provisioning, team orientation, and commencement of duties.
United Kingdom Right to Work & Skilled Worker Visa Guide
Employment in the United Kingdom requires legal Right to Work verified under the Home Office Points-Based Immigration System:
Sponsoring employers must hold an active Home Office A-rated Sponsor License and assign a valid Certificate of Sponsorship (CoS). Role must meet the general minimum salary threshold (£38,700) or occupation going rate.
Continuous employment under Skilled Worker status establishes eligibility for Indefinite Leave to Remain (ILR) after 5 continuous years, leading to British Citizenship.
Candidate Preparation Blueprint: Biotech & Pharmaceuticals
Based on transatlantic hiring benchmarks for Senior Manufacturing Scientist - Aseptic roles across Quotient Sciences's corporate sector, successful applicants typically excel across three core dimensions:
Demonstrated portfolio evidence, architecture/system design case studies, or validated professional certifications directly applicable to Biotech & Pharmaceuticals.
STAR method competency responses highlighting cross-functional leadership, conflict resolution, and delivering measurable enterprise ROI under tight timelines.
Total compensation expectation aligned within the benchmarked £21,770 - £23,354 bracket, including retirement vesting and health parity.
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