Supervisor ELISA & RIDS Manufacturing
Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation?
Do you want to make a difference?
If the answer is ‘yes’ then you’re just the kind of person we’re looking for!
We have a fantastic new opportunity for a Supervisor to work in or busy ELISA & RIDS Manufacturing department. The successful candidate will be in involved in:
- Ensuring that all manufacture and in-process testing within the department is performed and documented as required by the company quality, regulatory and legal requirements.
- Ensuring that all paperwork is completed correctly, ensuring the accurate transfer of data and calculations.
- Ensuring that all equipment used within the department is maintained & calibrated in accordance to the relevant SOP
- Providing support and guidance to technicians on matters of quality assurance, manufacturing & in-process testing, and to take appropriate action where errors are identified (with the support of their line manager, where required).
- Training members of staff in the tasks carried out within the department
- Addressing any CAPA’s and NCR’s assigned to the department and ensure effective completion of the various gates within the required timeframes
- To have an understanding and plan the capacity of their area of responsibility (including resource and equipment)
Ensure that issues are raised and escalated appropriately, with technical issues referred to the investigation team.
- Identifying problems / issues as they arise and be able to communicate these to appropriate members of staff and to suggest potential solutions and improvements.
- Line management responsibility for designated technicians.
- Scheduling the workload within your area of responsibility.
- Completing records and worksheets fully, clearly and legibly, at the time work is completed.
Essential:
- A relevant Scientific degree (or equivalent in work experience)
- Laboratory experience
- Previous experience of working within a quality management system
- Previous experience of using an ERP system
- Excellent communication skills (both written and verbal)
- Microsoft Office experience
- To be well organised/good time management with the ability to work work to deadlines
- The ability to multitask and prioritize
- Good analytical skills
- Excellent attention to detail
- To be flexible to the needs of the business
Desirable:
- Experience in a supervisory role
Working for us:
Founded in 1986 by a group of former researchers based at the University of Birmingham, Binding Site is today recognised as a market leader in the development of products for the investigation of a range of disorders involving immunodeficiency.
The Company is built on the success of its people and values them as its key asset. Integral to Binding Site is creating a diverse and inclusive culture which welcomes and creates diversity of thought, action, and innovation where all 1,200 colleagues can truly thrive. Support and continuous education is reinforced through partnerships with organisations such as Stonewall.
With a strong focus on building a sustainable future for its workforce and local communities, Binding Site has high aspirations for continuous improvement and ensuring their people contribute to their future vision. In addition, Binding Site has recently been recognised at the 2021 Birmingham Post Business Awards, winning both “Company of the Year” and “International Trade and Export” Awards.
Working at Binding Site means being part of a global, award-winning community that delivers innovative solutions with shared ideas and a collective dedication to improving patient lives, worldwide.
Location: Birmingham
Hours: 40 hrs
Benefits:
Competitive Salary
25 days paid holiday plus bank holidays
Pension- 6% contribution
Life Assurance
Medicash- Health Benefit