Quality Assurance Officer (Operations)

Quality Assurance Officer (Operations)

Temporary 29500 - 32000 £ / year (est.) No working from home possible
Acorn by Synergie

At a Glance

  • Tasks: Support batch release activities and investigate quality issues during the late shift.
  • Company: Acorn by Synergie recruits for a leading manufacturer in the pharmaceutical sector.
  • Benefits: Competitive salary of £29,500 - £32,000 plus additional shift premium.
  • Other info: Fixed-Term Contract (Maternity Cover) from 2 pm to 10 pm, Monday to Friday.
  • Why this job: Immediate opportunity to impact product quality in a regulated environment.
  • Qualifications: Minimum 2 years' experience in Quality Assurance within regulated manufacturing.

The predicted salary is between 29500 - 32000 £ per year.

Acorn by Synergie is recruiting on behalf of a leading manufacturer within the pharmaceutical and nutritional health sector for an experienced Quality Assurance Officer to join their Quality team on a maternity cover contract.

This is an excellent opportunity for a quality professional looking to play a key role in maintaining product quality, regulatory compliance and continuous improvement within a highly regulated manufacturing environment.

As the primary Quality representative on shift, you will work closely with Production, Operations and Technical teams to ensure products are manufactured to the highest quality standards. You will be responsible for supporting batch release activities, investigating quality issues, maintaining compliance with GMP requirements and driving a strong culture of quality across the site.

This role would suit someone with previous experience in pharmaceutical, nutraceutical, food manufacturing or other regulated production environments who enjoys problem-solving, collaboration and making a tangible impact on product quality and customer satisfaction.

Key Duties
  • Act as the main Quality point of contact during the late shift, providing guidance and support to production teams.
  • Ensure manufacturing processes and production areas remain compliant with GMP and relevant industry regulations.
  • Conduct batch record reviews and support timely product release activities.
  • Perform final product inspections in accordance with approved procedures and quality standards.
  • Investigate deviations, complaints and non-conformances, identifying root causes and supporting corrective actions.
  • Monitor and support CAPA activities to ensure effective resolution of quality issues.
  • Maintain accurate quality documentation and quality system records.
  • Support internal audits and contribute to external audit readiness.
  • Assist with KPI reporting, quality trend analysis and continuous improvement initiatives.
  • Support training and development of new team members.
  • Promote a strong quality culture and drive compliance across all operational activities.
Requirements
  • Minimum of 2 years' experience within a Quality Assurance, Quality Control or Quality Systems role.
  • Experience working in a regulated manufacturing environment such as pharmaceutical, nutraceutical, food, feed or FMCG.
  • Strong understanding of GMP principles and quality management systems.
  • Experience investigating deviations, complaints or non-conformances.
  • Excellent organisational skills and attention to detail.
Desirable
  • Degree or equivalent qualification in a STEM-related discipline.
  • Knowledge of ISO, FEMAS, pharmaceutical, food safety or related quality standards.
  • Internal auditing experience.
  • Experience supporting continuous improvement projects.
What We Offer
  • Competitive salary of £29,500 - £32,000 depending on experience.
  • Additional shift premium for late working hours.
  • Opportunity to join a respected and growing manufacturer.
  • Exposure to a highly regulated and quality-driven environment.
  • Collaborative team culture with opportunities to broaden your quality expertise.
  • Immediate opportunity to make a significant impact within the business.

Quality Assurance Officer (Operations) employer: Acorn by Synergie

Join a respected manufacturer in South Petherton, offering competitive salaries and a collaborative team culture. You'll work in a highly regulated environment, contributing to quality assurance in the pharmaceutical and nutritional health sector.

Acorn by Synergie

Contact Details:

Acorn by Synergie Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Assurance Officer (Operations)

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 Acorn by Synergie.

We think you need these skills to ace Quality Assurance Officer (Operations)

Quality Assurance
GMP Compliance
Batch Record Review
Product Inspection
Deviation Investigation
Root Cause Analysis
CAPA Management

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 Acorn by Synergie.

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 Acorn by Synergie. 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 Acorn by Synergie

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 Acorn by Synergie.

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 Acorn by Synergie 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.