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- Tasks: Conduct quality control tests and ensure compliance with industry standards.
- Company: Join Piramal Pharma Solutions, a leader in pharmaceutical development and manufacturing.
- Benefits: Full-time role with competitive pay and opportunities for growth.
- Other info: Dynamic work environment with a focus on continuous improvement.
- Why this job: Make a difference in healthcare by ensuring product quality and safety.
- Qualifications: Attention to detail and effective communication skills required.
The predicted salary is between 30000 - 40000 £ per year.
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients 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 like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
Job Description
To 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.
Key Roles/Responsibilities:
- Perform batch disposition and stability activities in a proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products and stability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFR part 11 Good Documentation Practices for Electronic Data.
- Perform stability study programme activities, storage of in process, and final products samples and retention sample management.
- System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department.
- Ownership and accountability of deviations, investigations and laboratory investigations and timely completion of these documents.
- Preparation and update of SOPs, instructions and protocols and other Quality Control documentation.
- Checking and reviewing of data in compliance with Data Integrity requirements.
- Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.
- Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration.
- Maintain Quality Control information systems.
- Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst.
- Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner.
- Attend internal and external scientific and technical meetings and conferences where appropriate.
- Carry out general maintenance and housekeeping of equipment and laboratories.
- Available to provide cover for other departments within the organisation as required.
- Available to undertake any other duties as requested by the QC Manager in accordance with Company requirements.
Competencies:
- Attention to detail
- Reliability
- Effective communication
- Understanding of scientific and technical processes
QC Analyst in Falkirk employer: Piramal Pharma Limited
Contact Detail:
Piramal Pharma Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst in Falkirk
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at Piramal Pharma Solutions. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your QC knowledge and the specific requirements of the role. We recommend practising common interview questions and having examples ready that showcase your attention to detail and problem-solving skills.
✨Tip Number 3
Don’t just wait for job postings! Keep an eye on our website and apply as soon as you see a QC Analyst position. The early bird gets the worm, and we love seeing proactive candidates!
✨Tip Number 4
Follow up after your interview with a thank-you email. It shows your enthusiasm for the role and keeps you fresh in the interviewer's mind. Plus, it’s a great chance to reiterate why you’re the perfect fit for the QC Analyst position!
We think you need these skills to ace QC Analyst in Falkirk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QC Analyst role. Highlight relevant experience and skills that match the job description, like your attention to detail and understanding of GMP practices.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control and how your background makes you a great fit for our team at Piramal Pharma Solutions.
Showcase Your Technical Skills: Don’t forget to mention any specific technical skills or experiences you have with QC equipment and processes. This will show us that you’re ready to hit the ground running!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and we can’t wait to see your application come through!
How to prepare for a job interview at Piramal Pharma Limited
✨Know Your QC Basics
Make sure you brush up on your knowledge of Quality Control processes and cGMP practices. Familiarise yourself with the specific tests and protocols mentioned in the job description, as this will show that you're serious about the role and understand what’s expected.
✨Prepare for Technical Questions
Expect to be asked about your experience with QC equipment and data integrity requirements. Be ready to discuss any relevant projects or situations where you had to troubleshoot issues or ensure compliance with regulations. This is your chance to showcase your problem-solving skills!
✨Showcase Your Attention to Detail
Since attention to detail is crucial for a QC Analyst, prepare examples from your past work where your meticulousness made a difference. Whether it was catching an error in documentation or ensuring accurate calibration of equipment, these stories will highlight your fit for the role.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the team dynamics, ongoing projects, or how they handle continuous improvement initiatives. This not only shows your interest but also helps you gauge if the company culture aligns with your values.