Production operator - #1089554

Baxter Global


Date: 1 week ago
City: Liverpool
Contract type: Full time
Work schedule: Full day
Baxter Global


Vantive: A New Company Built On Our Legacy


Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.


At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.


*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.


Summary


The Production Operator reports to the Team Leader working on shift as required, and has the responsibility to ensure daily production plan is met whilst adhering to Standards of Quality, Good Manufacturing Practice and EHS.


Our working hours are 2 days (7am to 7pm), 2 nights (7pm to 7am) and then 4 days off, on rotation.


Role Responsibilities

  • Operate the process plant used in the manufacture of Icodextrin. The Production operator must be fully trained and have full understanding of the operation of the production process from the Feed Preparation to the Spray Drying, including the EOC activities for RCB and/or WBB production lines.

  • Work under the guidance of the Team/Vice-Team Leader to perform and complete the assigned duties in timely manner.

  • Provide effective feedback to the Team Leader or Vice-Team Leader on relevant issues regarding product quality, documentation errors, EH&S and process issues in a timely manner.

  • Keep full records of all process operations carried out using appropriate batch documentation. The documentation must be completed per the GDP (good documentation practice), and any deviations from routine processing must be reported in writing on Batch Record Sheets.

  • To ensure area clearances are performed according to procedure in a timely manner.

  • Comply with EHS/GMP/GDP/company and corporate policies and external regulatory requirements.

  • To ensure that all duties are being carried out as per procedures and to the required standard.

  • To be aware of COSHH requirements and Risk Assessments for all activities and operations, new and existing, in the area.

  • Operate the utilities systems. Be fully trained in the operation of the site utilities and associated plant. Maintain the running logs. Identify any faults in their operation and report to the Team Leader/Vice Team Leader.

  • Operate pedestrian trucks to transfer the raw materials, consumable and final product between warehouse and process area.

  • Maintain standards of 6S and GMP within the production plant and stores keeping at all times the process area in a clean and tidy condition. Ensure that the cleaning cycles described in the operating instructions are carried out thoroughly.

  • Carry out the TPM activities scheduled for the day and report any issues found.

  • Ensure that the principles of Health and Safety at Work are adhered to. Be fully aware of the safety requirements, raise safety observation for each hazard identified and instruct any personnel coming about the PPE requirements.

  • Inspect equipment to identify any replacements, malfunctions and repairs.

  • Carry out routine maintenance operations in charge of the production department and support engineering/maintenance team when performing other maintenance tasks.

  • Evaluate equipment performance and recommend improvements.

  • Recommend process improvements to enhance operational efficiency and safety.

  • Contribute to waste management programs.

  • Ensure to adhere to company rules and work ethics.

  • Ensures company brand materials and physical working spaces meet and exceed company presentation standards.


Qualifications, Skills and Experience

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. 

  • Person with a strong work ethic and able to work flexibly to meet the needs of the business

  • Uncompromising commitment to Quality

  • Be safety cautious

  • Ability to communicate effectively, in writing and verbally.

  • Committed and supportive team player 

  • Accurate worker who enjoys getting the details right

  • Good PC skills (Microsoft Office)

  • Must be physically fit and active

  • 1-3 years working in a pharmaceutical company – Preferred not mandatory


What are some of the benefits of working at Baxter?

  • Competitive total compensation package

  • Competitive benefits

  • Professional development opportunities

  • High importance placed on work life balance

  • Commitment to growing and developing an inclusive and diverse workforce


#IND-UKOPS


Reasonable Accommodations


Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.


Recruitment Fraud Notice


Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

131580

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