At a Glance
- Tasks: Lead a QC team, manage lab practices, and ensure compliance in a pharmaceutical setting.
- Company: Dechra is a global leader in veterinary pharmaceuticals, dedicated to quality and innovation.
- Benefits: Enjoy a 36-hour work week, extra time off, training opportunities, and generous leave policies.
- Why this job: Join a supportive culture that values dedication, enjoyment, and personal growth while making a difference.
- Qualifications: Experience in a pharmaceutical lab and team management, with strong problem-solving and communication skills.
- Other info: Work on a 9-day fortnight schedule with shifts from 2pm to 10:30pm.
The predicted salary is between 42000 - 60000 £ per year.
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Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra.
Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.
Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2500 colleagues globally. From manufacturing to marketing, ( D )edication, ( E )njoyment, ( C )ourage, ( H )onesty, ( R )elationships and ( A )mbition are at the heart of our everyday operations and the way we do business.
The Opportunity
Reporting to the QC Manager and managing a team of Analysts and Senior Analysts, you shall enhance laboratory practices and promote a culture which is consistent with cGMP, cGLP and Health & Safety within a pharmaceutical laboratory environment.
Responsible for leading the Quality Control laboratory shift resources to achieve the required organisational throughput in a compliant and effective manner.
This role operates on a 9 day working fornight, with a shift pattern of 2pm – 10:30pm.
Role Responsibility
So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:
- Day to day management of the QC shift team, including: Staff performance and wellbeing, including routine 1-2-1s, target setting, and coaching individuals through any development needs. Coordinate resource priorities with Planning to achieve schedule adherence.
- Manage the throughput of inbound and outbound goods (primarily raw materials, intermediates and finished products) within the department.
- Support validation activities.
- Determination of KPIs that support delivery to service level agreements and achievement of objectives. Clear presentation of KPI data.
- Identification and management of risks.
- Preparation and scrutiny of reports (routine and ad-hoc), as required, to peers and senior management.
- Effective communication with other departments to facilitate the progression of QC activities.
- Lead investigations in to out of specification (OOS), out of trend (OOT) and a-typical results by applying technical knowledge and problem-solving skills.
- Ensure Quality Control activities are performed consistently, on time and in accordance with both company and legal requirements.
- Actively seek opportunities to optimise the performance of processes, people and other resources.
- Support the QC Manager with the hosting of departmental audits and inspections, including: Presenting the department and systems to an inspector. The compilation of responses. Ensure response commitments are fulfilled.
- Support the QC Manager in the delivery of departmental objectives and deputise, when required.
- Abide by and champion the company’s values (Dedication, Enjoyment, Courage, Honesty, Ambition) in all aspects of the role, including interaction with co-workers and third parties.
- In addition to the core responsibilities listed above, the jobholder may be required to perform other duties on an ad-hoc basis.
The Ideal Candidate
Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We’re particularly keen to hearfrom those who have/are:
- Experience of working within a pharmaceutical laboratory.
- Experience of leading and managing a team, with a focus on coaching/mentoring.
- Experience in chemical and instrumental techniques, such as; traditional wet chemistry, spectroscopy, chromatography, Karl Fischer, TOC, pH, etc.
- The ability to troubleshoot on the majority of the above / good problem-solving ability.
- Effective communication and influencing skills.
- Pragmatism.
- Computer literate with good attention to detail.
Package Description
- Average 36-hour working week (with a day off every other Friday!!)
- Lates, 14.00-2230
- Plenty of training and development opportunities
- 22.5 days annual leave + Bank holidays
- Option to buy a week\’s holiday each year
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QC Shift Manager - Lates employer: Dechra
Contact Detail:
Dechra Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Shift Manager - Lates
✨Tip Number 1
Familiarise yourself with Dechra's core values: Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition. During your interactions, whether in interviews or networking, demonstrate how your personal values align with theirs.
✨Tip Number 2
Highlight your experience in managing teams within a pharmaceutical laboratory setting. Be prepared to discuss specific examples of how you've coached and developed team members, as this is crucial for the QC Shift Manager role.
✨Tip Number 3
Brush up on your knowledge of chemical and instrumental techniques relevant to the role, such as chromatography and spectroscopy. Being able to speak confidently about these methods will set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your problem-solving skills and provide examples of how you've successfully handled out-of-specification results or other quality control challenges in the past. This will showcase your ability to lead investigations effectively.
We think you need these skills to ace QC Shift Manager - Lates
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the QC Shift Manager position at Dechra. Tailor your application to highlight relevant experience in managing teams and working within a pharmaceutical laboratory.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience with chemical and instrumental techniques, as well as any previous leadership roles. Use specific examples to demonstrate your problem-solving skills and ability to manage a team effectively.
Showcase Alignment with Company Values: Dechra values Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition. Make sure to weave these values into your application by providing examples of how you've embodied them in your previous roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in quality control.
How to prepare for a job interview at Dechra
✨Understand the Company Values
Before your interview, make sure you familiarise yourself with Dechra's core values: Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition. Be prepared to discuss how these values resonate with your own work ethic and experiences.
✨Showcase Your Leadership Skills
As a QC Shift Manager, you'll be leading a team. Prepare examples of how you've successfully managed teams in the past, focusing on coaching, mentoring, and performance management. Highlight any specific achievements that demonstrate your leadership capabilities.
✨Demonstrate Technical Knowledge
Brush up on your knowledge of chemical and instrumental techniques relevant to the role, such as chromatography and spectroscopy. Be ready to discuss how you've applied these techniques in previous roles and how you can troubleshoot issues that may arise.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities and decision-making skills. Think of scenarios where you've had to manage risks or lead investigations into out-of-specification results, and be ready to explain your thought process and outcomes.