Quality Controller
at Medik8
Aylesbury HP22 5WJ, , United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 14 Feb, 2025 | Not Specified | 16 Nov, 2024 | N/A | Good communication skills | No | No |
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Description:
Medik8 is an award-winning skincare brand that is rapidly expanding across the globe.
Not only are our formulations crafted in our on-site facilities in the UK, our products are blended and packaged here, too.
Our Quality Team strives for excellence and continuous improvement. They ensure that all processes, from raw materials to finished goods, are in compliance with company and quality standards, and that compliance with GMP is maintained at all times.
In this role, you will foster a ‘quality-first culture’ by working within the quality team to ensure product meets and exceeds the high standards expected of our customers.
You will be based at our Innovation Centre in Aylesbury where we will have state-of-the-art skincare suited laboratory, modern manufacturing rooms and logistics site. This will be our hub where the best synergies can be created; where we can drive deeper research, boost innovation and maintain exceptional quality levels.
We don’t focus simply on what we do – we also care how we do it. Our values and the way we behave are extremely important to us. If you want to work in a fast paced operational environment where you will receive guidance and mentoring to develop your knowledge and skills then apply now!
The shift for this role is 2:30pm-11pm and is based on site 5 days a week.
ABOUT US
Medik8 is an established leader in the skincare arena, utilising our iconic CSA Philosophy to develop professional anti-aging solutions that ensure Beautiful Skin For Life.
After seeing incredible growth over the last few years, we became PE backed in 2021. This investment will allow us to expand even faster, to innovate the future and to take on the world with our award-winning products in all the categories.
WANT TO DO A LITTLE MORE RESEARCH BEFORE YOU APPLY?
Head over to our main careers page to find out more about the team and our values. You can also find out more about us on Linkedin, Glassdoor & Instagram.
At Medik8, we believe that diversity within our workplace drives innovation. We celebrate multiple backgrounds, cultures, approaches and points of view, and believe that when people feel respected and included, they can truly flourish. We’re committed to advancing equal opportunities and we’re dedicated to building a workforce as diverse as our consumer base, creating a multifaceted, equitable and inclusive culture and allowing all colleagues to bring their whole selves to work.
Our DE&I ethos also flows through our recruitment process. Studies have found that minority groupings tend to apply for roles only when they meet 100% of the role requirements, in comparison to non-minority grouping tend to apply when they meet only 60% of the role requirements (Hewlett Packard ). The requirements listed in our job descriptions are guidelines, not hard and fast rules, so if you think you meet 60+ of the role spec and are passionate, excited & feel like you have the potential to fulfil the rest - then we want to hear from you
Responsibilities:
- Performs QC inspections in Goods In, Bulks and in the manufacturing area to ensure quality standards are maintained.
- Provide Quality support for the operational teams.
- Deviation management - perform impact assessments for deviations, identify root cause and raise CAPAs. Facilitate investigations to prompt closures within timelines.
- Review batch documentation to ensure compliance with written instructions.
- Review and update SOPs/WIs, when required.
- Continually improves standards, monitors hygiene, quality and products safety issues on a daily basis.
- Identifies and reports any issues in accordance with company procedures and supports deviation/complaint investigations.
- Guarantees success of ad hoc projects to improve the smooth running of the production and logistics processes.
We would love to hear from you if you…
- Have experience in a similar role, in a GMP/ manufacturing environment.
- Have good organisational skills and a methodical approach to work.
- Take pride in your work, paying close attention to details.
- Have excellent written and verbal communication skills.
- Can work independently and with minimal supervision.
- Are confident in taking accountability for quality standards across the PM teams.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Aylesbury HP22 5WJ, United Kingdom