Quality Control (QC) Analyst

Veranova Edinburgh, Scotland, United Kingdom

Who We Are:
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview:
An exciting opportunity has arisen for a Quality Control (QC) Analyst to join our team on a permanent basis in our Quality Control Department. The job holder will be required to perform analysis in support of Production, Quality, and Development activities in the manufacture of pharmaceuticals and fine chemicals.

Core Responsibilities:

• Conduct Development Department, Out of Specification, Process Validation, Method Validation and other miscellaneous analysis, as requested by the Head of Quality Control, Group Leader or nominated deputy, according to the written procedures of the company, pharmacopoeia and regulatory requirements.
• Liaise with Development Department staff when conducting development sample analysis and method validations.
• Report any out of specification or anomalous result to a supervisor and document any deviations from written analytical procedures.
• Assist in the investigation of out of specification or anomalous results.
• Operate documented systems to ensure that duties are performed to, and maintain GMP standards.
• Perform and document routine calibration and general laboratory duties as directed by the Head of Quality Control, Group Leader or nominated deputy.
• Assist in the preparation of method validation protocols and reports, Development reports, SOP's, specifications and analytical methods as requested by the Head of Quality Control, Group Leader or nominated deputy.
• Assist in the provision of induction training to new members of the department.
• Perform duties in a safe and efficient manner.
• Any other duties as reasonably requested.

Qualifications:

• Degree in Chemistry or closely related subject.
• Analytical experience in QC or laboratory support environment working in cGMP.
• Excellent analytical, written, and verbal communication skills.
• Good attention-to-detail, good judgment, and problem solving.
• Accountability for your work and good observational skills.
• Accuracy, integrity, honesty and reliability.
• Ability to be flexible to meet the needs of the department and wider business.

Our Commitment:

• Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.
• Financial Wellness: The company provides an industry-leading compensation package, and this position is eligible for an annual performance bonus in accordance with the terms of the applicable bonus plan. You will also receive excellent pension contributions with the option of making contributions via salary sacrifice and access to discounts from major online and high street stores.
• Health & Wellbeing: As well as being entitled to 25 days’ annual leave plus recognised Scottish public holidays, our colleagues are also eligible to participate in benefits such as our Health Shield Cash Plan, Cycle2Work Scheme, life insurance, income protection, and GP Anytime.
• Professional Development: Opportunities for continuous growth and development through resources such as LinkedIn Learning, functional career pathways, and individual Personal Development Plans to map out your future with us.

How to Apply:
At Veranova, we are eager to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit www.veranova.com to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise.

We value a diverse range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed.

If you are a member of the Armed Forces, first responder, or are in the process of transitioning from the Armed Forces to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.

For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to talentacquisition@veranova.com in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability.

Additional Information:
Under UK legislation, we are required to ensure that all employees have the legal right to work in the UK, both at the time of offer and throughout their employment. Please note that we are not able to provide sponsorship for this role, so applicants must have the necessary right to work in place independently.

Veranova is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.

Seniority level

Entry level

Employment type

Full-time

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing