Quality Control Supervisor - Label Control/Distribution (Job Share)
Part-time, Permanent Who We Are
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients. Skills and Attributes
Supervisory experience Knowledge of GMP Quality Control Description
The Role As the QC Supervisor, your primary responsibility is to manage and develop a team to ensure the effective and timely delivery of Quality Control (QC) activities. You will be accountable for ensuring GMP compliance, meeting customer expectations, and adhering to regulatory demands. In your role, you must maintain a regular presence on the floor managing personnel, fostering a positive working environment, monitoring team performance, and ensuring documentation is complete, auditable, and in compliance with cGMP. Additionally, you will act as the quality representative/subject matter expert on assigned projects, report any serious breaches in GMP compliance, assist management in the preparation and delivery of data for customer/supplier teleconferences, and fulfill any necessary administrative duties associated with the role. You will support, coach, and mentor team members and ensure training records are up to date. Your technical duties include reviewing and approving GMP documentation, supporting investigations and root cause analysis, ensuring follow-up actions assigned to you or your direct reports are actioned, actively considering opportunities for business improvement, and engaging with global counterparts to gain agreement. In summary, the QC Supervisor role requires a highly organized, collaborative, and detail-oriented individual with strong communication, people-management, and technical abilities to deliver high-quality QC activities. Key Requirements
Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full-time employment in the UK Level 5/HND qualification OR significant relevant supervisory experience Previous experience working to specified Quality standards/guidelines Degree level (or equivalent) qualification within a Life Science discipline Experience within a supervisory role Experience in a Pharmaceutical/GXP environment Further Information
This position is based on 40 hours per week. These hours will be split between you and your job share partner. Your minimum hours of work will be 20 hours average per week as part of the Job Share arrangement. Your working pattern will be based on permanent evening shift: Week 1
– Monday & Tuesday – 15:00 – 23:30 Week 2
– Monday, Tuesday & Friday – 15:00 – 23:30 Please note that you will be required to cover the role of your job share partner during periods of illness, holidays, or other absence (both planned and unplanned). Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date
We will no longer be accepting applications after 5pm on
07 January 2025 . RECRUITMENT AGENCIES PLEASE NOTE:
Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation. Almac Group is an Equal Opportunity Employer.
#J-18808-Ljbffr
Part-time, Permanent Who We Are
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients. Skills and Attributes
Supervisory experience Knowledge of GMP Quality Control Description
The Role As the QC Supervisor, your primary responsibility is to manage and develop a team to ensure the effective and timely delivery of Quality Control (QC) activities. You will be accountable for ensuring GMP compliance, meeting customer expectations, and adhering to regulatory demands. In your role, you must maintain a regular presence on the floor managing personnel, fostering a positive working environment, monitoring team performance, and ensuring documentation is complete, auditable, and in compliance with cGMP. Additionally, you will act as the quality representative/subject matter expert on assigned projects, report any serious breaches in GMP compliance, assist management in the preparation and delivery of data for customer/supplier teleconferences, and fulfill any necessary administrative duties associated with the role. You will support, coach, and mentor team members and ensure training records are up to date. Your technical duties include reviewing and approving GMP documentation, supporting investigations and root cause analysis, ensuring follow-up actions assigned to you or your direct reports are actioned, actively considering opportunities for business improvement, and engaging with global counterparts to gain agreement. In summary, the QC Supervisor role requires a highly organized, collaborative, and detail-oriented individual with strong communication, people-management, and technical abilities to deliver high-quality QC activities. Key Requirements
Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full-time employment in the UK Level 5/HND qualification OR significant relevant supervisory experience Previous experience working to specified Quality standards/guidelines Degree level (or equivalent) qualification within a Life Science discipline Experience within a supervisory role Experience in a Pharmaceutical/GXP environment Further Information
This position is based on 40 hours per week. These hours will be split between you and your job share partner. Your minimum hours of work will be 20 hours average per week as part of the Job Share arrangement. Your working pattern will be based on permanent evening shift: Week 1
– Monday & Tuesday – 15:00 – 23:30 Week 2
– Monday, Tuesday & Friday – 15:00 – 23:30 Please note that you will be required to cover the role of your job share partner during periods of illness, holidays, or other absence (both planned and unplanned). Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date
We will no longer be accepting applications after 5pm on
07 January 2025 . RECRUITMENT AGENCIES PLEASE NOTE:
Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation. Almac Group is an Equal Opportunity Employer.
#J-18808-Ljbffr
