As an Calibration & Instrumentation Engineer, you will ensure the accuracy and reliability of measurement instruments and equipment used in drug manufacturing processes. This role involves developing and implementing calibration procedures, performing routine calibrations, and maintaining detailed records to ensure compliance with regulatory standards such as those set by the regulations and standards. The engineer ensures that all instruments provide precise measurements critical for maintaining product quality, safety, and consistency. Additionally, support continuous improvement initiatives, troubleshoot measurement issues, and provide technical training to staff.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
Key Responsibilities:
- The occupant of this job title shall primarily be accountable for maintaining, developing and updating the calibration and instrumentation Maintenance systems across GSAL site.
- The Occupant shall also be required to stand in for Electrical Officer position during vacation.
Accountability:
- Responsible to carry out the calibration of the site validated devices according to the Group related policy ,the approved procedures , the approved acceptance limits and scheduling in order to assure the operation as per validated parameters . This includes all CMMS listed devices in utilities (electromechanical), production and quality assurance areas.
- Responsible to communicate all out of calibration devices to relevant owners as per SOP.
- Responsible to ensure full compliance of the calibration system with GQP 4304 latest requirements as applicable to the site.
- Responsible to ensure that all used calibration SOP‘s and Routines are the approved and valid copy.
- Responsible to ensure that the calibration Master file , the Raw data log book , the Calibration Acceptance Criteria list and the Transfer of standards are all kept up to date and in Audit Readiness Status
- Responsible to ensure that all used reference standards are having valid calibration that is traceable to approved international standards.
- Responsible to ensure the calibration lab (RM423) is kept in organized and clean status and only applicable and up to date documentation is filed in the room in line with retention policy GQP3301.
- Responsible for routine maintenance of Building Management System and utility programmable controllers according to manufacturers recommendations and as specified in the “PPM’’ Planned Preventive Maintenance
- Responsible for carrying out breakdown maintenance and troubleshooting of the programmable controllers.
- Responsible for ensuring that all control systems Programmable and Configurable software storing media are maintained and controlled as per (ELE/SOF/412) standard operating procedure.
- Ensure the use of CMMS system to record all routine and incidental maintenance, review breakdown history and update the PPM routines as preventative measure.
- Operate to new and established SOP”s designed to ensure that all related systems and engineering documentation are kept up to date and meets the current Glaxo Group, Local and International Standards.
- Ensure that all authored SOP ‘s are kept up to date
- Supervise / Carry out modifications related to systems engineering changes or capital projects.
- Supervise all electrical works including break downs, maintenance and safety related issues.
- Supervise all electrical works related to new project & modification carried all over the site.
- Work closely with other team members as and when required.
- Ensure that OEM manuals are kept updated and available at point of use.
- Ensure that all the time adequate spare parts are available for each system.
- Ensure that all tools and test equipment are kept in a safe and calibrated state prior to use.
- Attend and positively respond to training courses to improve work skills.
- Ensure that at all time the training record is kept up to date and in Readiness for Audit.
- Keep the logbooks (ELBs) maintained and up to date.
- Comply with all site and relevant Standard operating procedures.
- Ensure that validation /re validation of the related systems is carried out as per company procedure.
- Strictly adhere to Glaxo Environmental, Health and Safety instructions as per site EHS Policy and Procedures to prevent accidents and deliver EHS Targets.
- Act as First Aid team member.
- Ensure the reporting of up normal Incidents, Conditions or Near Misses that may result in damage to other GSK staff, property or reputation.
- Comply with all related Group Quality Policies requirement.
- Actively participate in the Operational Excellence initiatives & projects (i.e. OE, JDI, Lean Sigma. etc) to ensure optimum systems running cost.
- Ensure full familiarity and Implementation of all applicable GSK Corporate Governance Policies.
- Ensure the reporting of up normal Incidents, Conditions or Near Misses that may result in damage to other GSK staff, property or company reputation.
- Accountable for individually identified risks and escalate to the line manager, where applicable develop risk mitigation plan and monitor the implementation plan
- Complexity
- Degree of change & uncertainty; level of influencing required; degree of matrix working
- Analyze and put preventative measure for many faults that could happen at any area and
- Could be due to electrical/ Mechanical /instrumentation for different root causes, increasing amount of pressure when production is impacted.
- Communicate with maintenance supervisors and other departments stack holders for improvements.
- Ensure full familiarity and Implementation of all applicable Global Engineering Standards (GES) & insure compliance
- Adhere to L1, L2,L3 & L4 Audit schedule & ensure timely CAPA closure.
- Identify & escalate Risks & updating sectional Risk Log
- Carry out problem solving sessions when required
- Zap Reporting & Closure
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
- Bachelor’s degree in engineering (Mechanical/Electrical/ Electromechanical)
- Good knowledge of GMP and validation procedures.
- Good command of spoken and written English Language.
- Computer Skills (PC use, MS Office: Excel, Word. etc.).
Closing date:
01/04/2025
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
Contact information:
You may apply for this position online by selecting the Apply now button.
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