Manufacturing Team Leader
Job Description
About us
Bristol Laboratories Ltd is one of the leading and fastest growing pharmaceutical companies in the United Kingdom engaged in the development, manufacturing, marketing and distribution of generic medicines, as well as formulation brands. We have state-of-the art manufacturing facilities in Luton & Peterlee.
As a result of continued growth and expansion, we have an excellent opportunity to appoint Manufacturing -Team Leaders.
About the Role:
We are looking for Team Leaders who hold degree/diploma in Pharmaceutical Science & have recently graduated. We are keen to hire candidates who are looking to start their career with a challenging profile.. This role will be based on a rolling contract to begin with and potential to become permanent in future. The role will involve meticulous planning and execution of various activities within the manufacturing department. The role will also involve working with other departments to meet production targets while meeting the MHRA and cGMP compliance standards.
Key Responsibilities
- Manage & organize production personnel to meet agreed production schedules and targets.
- Assist Manager in conducting department trainings and other routine activity.
- Check, review and verify all documentation & process are in accordance with SOP/MBR in Manufacturing prior to operation and during operatio from raw material stage to finished product stage.
- Check line clearance of machines as per SOP.
- Carry out calibration of scales/balances and all other equipment at the required intervals as per the SOP’s/schedule.
- Preparation and regular review of SOP relating to the area of responsibility assigned.
- Observe standards of safety, quality and conduct with respect to yourself, colleagues and product.
- Use material handling equipment and manual handling techniques for movement of materials and equipment.
- Follow S.O.P. and B.M.R instructions for all operation / cleaning activities in the area.
- Review of batch record.
- Initiate CCP and CAPA in QAMS as and when required and maintain documentation as per cGMP in manufacturing area.
- Report out of specification product if any and any incidents, deviations or accidents to the department head.
- Follow the Good documentation practice and current Good manufacturing practice
- Carry out any other job in any other area/department as assigned by the department head.
About You:
- A minimum Science education with specialising in Pharmaceutical Science
- As a person, you have excellent communication and interpersonal skills, able to liaise with stakeholders at all levels and navigate cultural differences with ease.
- With strong organisation and administration skills, you make good decisions, have a strong eye for detail and can prioritise a busy workload to meet deadlines.
Reward:
- In return, we offer a competitive salary and rewards package.( Holidays, Free Parking, Occasional Opportunity to travel to different locations, attend seminars and meet industry experts)
- A fantastic training & development opportunity for someone seeking to enhance their learning in a challenging and fast-paced environment.
- Opportunity to grow further in your career by interacting and engaging with stakeholders at all levels.