At a Glance
- Tasks: Ensure top-notch quality and compliance through testing and data analysis.
- Company: Join a leading pharmaceutical company dedicated to innovation and excellence.
- Benefits: Competitive pay, flexible hours, and opportunities for professional growth.
- Other info: Dynamic team environment with potential for contract extension.
- Why this job: Make a real difference in healthcare by ensuring product quality and safety.
- Qualifications: Degree in chemistry or related field with relevant QC experience.
The predicted salary is between 33750 - 41250 £ per year.
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization.
The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation.
This position enhances QC efficiency and effectiveness.
Key Responsibilities
- Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
- Support weekend lab operations and maintain training records.
- Assist in lab equipment and inventory maintenance, including reagent and sample prep.
- Review data timely and qualify as a data reviewer Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
- Contribute to updating controlled documents (SOPs, work instructions, test methods).
- Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration.
- Support regulatory submissions, inspection readiness, and audits.
- B. S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
- Experience in method transfer/implementation; understanding of method lifecycle management.
- Strong technical writing, data analysis, problem-solving, and organizational skills.
- Proficiency in Lab Ware LIMS, Excel, Word, and Power Point.
- Contract position with possible extension
- Location: Norton, MA, with occasional responsibilities at other locations.
- Weekend coverage is required.
- First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
- #J-18808-Ljbffr
Quality Control Analyst II employer: BioPharma Consulting JAD Group
As a Quality Control Analyst II at our Norton, MA location, you will join a dynamic team dedicated to upholding the highest standards of quality and compliance in the pharmaceutical industry. We pride ourselves on fostering a collaborative work culture that encourages continuous improvement and professional growth, offering opportunities for skill enhancement and career advancement. With a commitment to employee well-being, we provide flexible scheduling options and a supportive environment that values your contributions and promotes work-life balance.
Contact Details:
BioPharma Consulting JAD Group Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Analyst II
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like BioPharma Consulting JAD Group.
We think you need these skills to ace Quality Control Analyst II
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at BioPharma Consulting JAD Group.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at BioPharma Consulting JAD Group. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at BioPharma Consulting JAD Group
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with BioPharma Consulting JAD Group.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help BioPharma Consulting JAD Group achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
