Process Technician Senior Coordinator (Fixed Term Contract / Site Based - Kent Science Park)

Jazz Pharmaceuticals; Sittingbourne; On-site; GBP 27,000 - 35,000; Full time

Job summary

Jazz Pharmaceuticals is seeking a Process Technician Senior Coordinator based in Sittingbourne, Kent. The successful candidate will oversee the processing of refined extracts while adhering to Health and Safety and cGMP standards. Responsibilities include managing manufacturing documentation, training new employees, and improving manufacturing processes. Candidates should have at least 2 years' experience in a regulated production environment and a good understanding of Microsoft Office. This position offers an opportunity to contribute to the growth of the department and ensure quality standards are met.

Qualifications

• Minimum of 2 years’ experience in a regulated production environment, preferably pharmaceutical/chemical or food industry.
• Ability to demonstrate excellent attention to detail.

Responsibilities

• Ensure compliance with health, safety, and cGMP standards.
• Aid in manufacturing processes by authoring and updating SOPs and documentation.
• Train and coach new employees on BDS manufacturing processes.
• Contribute to process improvements for efficiency and cost reduction.

Skills

Experience in regulated production environment

Good numeracy skills

Effective communication

Proficiency in Microsoft Excel and Word

Attention to detail

Ability to work independently and in a team

Positive relationship building

Problem-solving attitude

Capacity to assist colleagues

Education

Qualifications in the pharmaceutical industry (e.g., NVQs)

Job description

Please note this is a site based position in Kent Science Park.

The Process Technician Senior Coordinator is responsible for processing refined extract and its intermediates using a series of well-defined and documented manufacturing processes/procedures whilst being in compliance with Health and Safety (H&S) and current Good Manufacturing Practices (cGMP) requirements.

Essential Functions/Responsibilities

• Carries out their work in a way that will not adversely affect their own or others’ health, safety and security or the environment and reports any shortcomings in Jazz arrangements.

• The Job Holder has legal duties under the Health and Safety at Work Act, 1974 requiring them to take reasonable care for their own and others' safety, cooperate with employer safety measures (like training and policies), use equipment correctly, and report hazards or defects.

• Responsible for the manufacture of BDS in accordance with cGMP standards, both as an Initiator and Checker.

• Ensures that all activities undertaken comply with H&S and cGMP standards as detailed in relevant SOPs and working practices.

• Authors and updates batch documentation, standard operating procedures and associated forms.

• Responsible for the completion of quality related documentation, such as Deviations, CAPAs, Protocols and Change Controls.

• The nature of the work requires the Job Holder to be flexible with regards to working hours to ensure that they are available to complete a production process should it overrun.

• Ability to work across all Production Departments ie within the BDP Areas when fully trained.

• Trains and coaches new starters (re‑trained individuals) in BDS manufacturing processes.

• Looks for areas of improvement across all BDS manufacturing processes in order to improve efficiency and reduce costs.

• Informs line management of any atypical events/deviations immediately.

• Executes additional tasks in order to meet departmental objectives.

• Potential to act as the BDS Department H&S representative and undertake all of the tasks associated with that role.

• Potential to take responsibility for consumable and Critical to Quality ordering within the department.

Required Knowledge, Skills, and Abilities

• A minimum of 2 years’ experience gained in a regulated production environment, ideally within the pharmaceutical/chemical or food industry.

• Good level of numeracy.

• Good communication skills including written.

• A good working knowledge of standard Microsoft packages ie Excel and Word.

• The ability to work on own or in a small team environment.

• Excellent attention to detail.

• Develops and maintains positive working relationships with key stakeholder groups, both internal and external.

• Prepared to challenge the norm and look for areas of improvement share own ideas and information.

• Good team worker and assists colleagues as and when required.

• Demonstrates a ‘can do’ attitude.

Required/Preferred Education and Licences

• Ideally holds qualifications gained in the pharmaceutical industry ie NVQs or similar.