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- Tasks: Supervise and execute quality control tests for pharmaceutical products.
- Company: Piramal Pharma Solutions, a leader in drug development and manufacturing.
- Benefits: Inclusive workplace, career growth, and commitment to ethical practices.
- Why this job: Join a dynamic team making a real impact in healthcare.
- Qualifications: Experience in quality control and strong analytical skills.
- Other info: Collaborative environment with opportunities for continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board.
BUSINESS: Piramal Pharma Solutions
DEPARTMENT: Quality Control
LOCATION: Grangemouth
Job Overview
To supervise and execute defined and trained Quality Control department tests for the release of raw materials, in process products, bulk drug substance, final products and stability products according to defined procedures and protocols and according with best cGMP work practices, Quality standards and metrics.
Reporting Structure
Reports to QC Team Leader (Clinical ADC)
Key Roles/Responsibilities
- Execute analytical procedures for testing of raw materials, in process products, bulk drug substance, final products and stability products according to defined by SOP's, and protocols and ensure that the QC team is in compliance with the same.
- Apply best cGMP work-practices and techniques to test and release raw materials, in process products, bulk drug substance, final products and stability products within specification.
- Ensure that all QC analysts are appropriately trained and competent in the procedures they are conducting, and are in compliance with best cGMP working practices at all times.
- Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data provided by the QC Analysts.
- Immediately escalate and report any deviations to materials, facilities, processes or procedures to the QC Manager.
- Be accountable for the analytical laboratories being clean, tidy and well organized and in a state of continuous inspection readiness.
- Conduct all activities in the most careful and safe manner and in full compliance with ESH requirements.
- Ensure that at any time equipment, facilities and materials used in the area of responsibility comply with defined standards.
- Issue, manage and close-out deviations, change controls, OOS or SST investigations and CAPA's in a timely fashion.
- Identify areas for continuous improvement and escalate those to the QC Manager.
- Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team-setting.
- Support installation, qualification and periodic review of equipment.
- Support the transfer of new methods and techniques into Quality Control.
- To undertake any other duties as requested by the line manager in accordance with company requirements.
About Us
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
Equal employment opportunity
Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.
About the Team
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited's investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.
Senior QC Analyst in Falkirk employer: Piramal Group
Contact Detail:
Piramal Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Analyst in Falkirk
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that Senior QC Analyst role.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with your own. We want you to show them that you’re not just a fit for the role, but also for the team at Piramal Pharma Solutions.
✨Tip Number 3
Practice common interview questions and have your own questions ready. This shows you’re genuinely interested in the position and the company. We recommend focusing on how you can contribute to their quality control processes and continuous improvement initiatives.
✨Tip Number 4
Don’t forget to follow up after your interview! A simple thank-you email can go a long way in keeping you top of mind. We believe this small gesture can demonstrate your enthusiasm for the role and your professionalism.
We think you need these skills to ace Senior QC Analyst in Falkirk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior QC Analyst role. Highlight relevant experience and skills that match the job description, especially around cGMP practices and analytical procedures.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for our team. Share specific examples of your past work in quality control and how you’ve contributed to compliance and continuous improvement.
Showcase Your Team Spirit: We love a collaborative environment! Mention any experiences where you’ve worked well in a team, especially in training others or leading projects. It’s all about showing us you can contribute to our supportive culture.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Piramal Group
✨Know Your cGMP Standards
Make sure you brush up on current Good Manufacturing Practices (cGMP) before your interview. Being able to discuss how you've applied these standards in your previous roles will show that you're not just familiar with the regulations, but that you can implement them effectively.
✨Demonstrate Analytical Skills
Prepare to talk about specific analytical procedures you've executed in the past. Bring examples of how you’ve tested raw materials or final products, and be ready to explain the outcomes and any challenges you faced during those processes.
✨Showcase Team Leadership
As a Senior QC Analyst, you'll likely be supervising others. Think of instances where you've trained or mentored team members. Highlight your ability to foster a collaborative environment and ensure compliance with protocols, as this will resonate well with the hiring team.
✨Be Ready for Problem-Solving Questions
Expect questions about how you handle deviations or out-of-specification results. Prepare a couple of scenarios where you identified issues, escalated them appropriately, and contributed to corrective actions. This will demonstrate your proactive approach to quality control.
