QC Technical Project Manager

QC Technical Project Manager

Full-Time 50000 - 60000 £ / year (est.) No working from home possible
Blackfield Associates

At a Glance

  • Tasks: Lead technical projects in a QC lab, ensuring compliance and high-quality standards.
  • Company: Join a leading pharmaceutical manufacturer with a focus on innovation and quality.
  • Benefits: Competitive salary, career growth, and the chance to work with cutting-edge technology.
  • Other info: Dynamic role with opportunities for continuous improvement and professional development.
  • Why this job: Make a real impact in healthcare by ensuring the quality of life-saving medicines.
  • Qualifications: Degree in a scientific field and experience in QC systems and project management.

The predicted salary is between 50000 - 60000 £ per year.

Are you an experienced Quality Control professional with a passion for laboratory technology, compliance, and project leadership? We are recruiting for a QC Technical Project Manager to join a leading pharmaceutical manufacturing organisation, where you will play a pivotal role in driving technical projects, managing laboratory systems, and supporting the delivery of high-quality medicines.

The Role

Reporting to the Head of Quality Control, you will be responsible for managing all technical projects within the QC laboratory. This includes leading a team of technical specialists, overseeing laboratory electronic systems such as LIMS and CDS, introducing new technologies, managing equipment lifecycle plans, and ensuring compliance with GMP and Data Integrity requirements.

You will act as the technical lead for key laboratory initiatives, including new product introductions, analytical method transfers, system upgrades, validation activities, and global compliance programmes.

Key Responsibilities

  • Lead and develop a team of QC Technical Specialists, ensuring strong performance and resource planning.
  • Manage laboratory equipment and electronic systems to ensure compliance with GMP and Data Integrity requirements.
  • Deliver technical projects involving equipment procurement, qualification, validation, and implementation.
  • Maintain a long-term equipment replacement strategy to support future laboratory needs.
  • Lead new product introduction, method transfer, and compliance-related activities.
  • Oversee change controls, deviations, and validation activities associated with laboratory systems and equipment.
  • Collaborate with IT teams, external vendors, and cross-functional stakeholders to ensure systems remain effective and compliant.
  • Drive continuous improvement initiatives across QC operations and technology platforms.
  • Support audits, inspections, regulatory submissions, and responses to technical enquiries.
  • Champion data integrity and best practices across the laboratory environment.

About You

We are looking for a technically strong quality professional who combines project management expertise with a deep understanding of laboratory systems and pharmaceutical quality standards.

Essential Requirements

  • Degree in a scientific discipline or equivalent industry experience.
  • Strong knowledge of pharmaceutical QC equipment, laboratory systems, qualification, and validation activities.
  • Previous experience managing QC equipment and electronic systems within a regulated environment.
  • Experience working with laboratory software platforms such as LIMS and CDS.
  • Thorough understanding of GMP regulations and Data Integrity principles.
  • Proven ability to lead technical projects and deliver results to agreed timelines.
  • Strong communication and stakeholder management skills.
  • Ability to analyse complex technical information and communicate it clearly.

Key Competencies

  • Leadership and team development
  • Project and change management
  • Problem solving and decision making
  • Continuous improvement mindset
  • Strong organisational skills and attention to detail
  • Excellent verbal and written communication
  • Technical expertise combined with commercial awareness
  • Ability to work independently and influence stakeholders at all levels

QC Technical Project Manager employer: Blackfield Associates

At Blackfield Associates, we pride ourselves on being an exceptional employer, particularly for the role of Plant Quality Manager in Folkestone. Our commitment to fostering a collaborative work culture is complemented by robust employee growth opportunities and a focus on continuous improvement, ensuring that our team members thrive both personally and professionally. With a strong emphasis on quality and regulatory compliance, we offer a dynamic environment where your expertise will be valued and your contributions will directly impact our success.

Blackfield Associates

Contact Details:

Blackfield Associates Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land QC Technical Project Manager

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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Blackfield Associates.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Blackfield Associates. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Blackfield Associates is looking for. A tailored application can really make you stand out!

We think you need these skills to ace QC Technical Project Manager

Quality Control
Laboratory Technology
Project Leadership
GMP Compliance
Data Integrity
LIMS
CDS

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Blackfield Associates!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Blackfield Associates that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Blackfield Associates!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Blackfield Associates, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Blackfield Associates

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Blackfield Associates that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Blackfield Associates’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.