Sr Pharmaceutical Technician
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Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Flex 12 hr shift/nightsEnvironmental Conditions
Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Cold Room/Freezers -22degreesF/-6degrees C No contact lens allowed; prescriptive glasses will be provided Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job Description
PLEASE NOTE: This is a 12-hours rotating shift role
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Whenyourepart of the team atThermoFisher Scientificyoulldo important work. Surrounded by collaborative colleaguesyoullhave the support and opportunities that only a global leader can give you. Our respected growing organization has an outstanding strategy for the near term and beyond. Take your place on ourstrong teamand help us make meaningful contributions to the world.
The incumbent will perform various tasks and activities listed below for which they are appropriately trained andare in compliance withthecGMP company and department SOPs and the safety regulations.
Responsibilities
- Setup andoperatepharmaceutical production equipment including high-speed filling lines for sterile productsautoclavepartsand vial washersdepyrogenationtunnelformulation processHMIand automatic CIP/SIP processes as well asinspection and packaging line equipment (e.g.AVIM labelling and carton machine etc.) as per relevant SOPs and the Batch Record.
- Responsible for formulation activities of production batches whichincludesformulation and/or dispensing of all the availabledrug substance(s) and excipients.
- Responsible forparts preparationwashingand sterilization of materials.
- Responsible for packaging andtransfer ofthe final product to Freezer.
- Always complete all the relevant training before performing any task.
- Responsible to perform all the materials and process (SAP) transactions at each manufacturing processsteps.
- Strictly follow aseptic techniques andpractices practicefor aseptic operations.
- Carry out the cleaning and upkeepof the production equipment and classified areas inmanufacturingarea.
- Perform routine QC sampling and in-process testing of the product at various stages throughout manufacturing (e.g.bioburden sampling waler sampling) and chemical and physical tests during the processing of the batch (e.g.pH testing) if applicable.
- Timely completion of relevant batchrecordand logbooks for the tasks performed and with adherence to GDP (Good Documentation Practice).
- Transfer materials for manufacturinga batch.
- Prepare filters for test execution and perform FIT (filter Integrity testing).
- Provide forthe loading/unloading of the loads/batch from the equipment during production activities.
- Perform stock check of consumables and inform Manager/Lead technician for required materials.
- Follow safety and quality compliance at all timesand communicatein a timely mannerto theManagerif any anomalies areobserved.
- Participate in EHS Business CompliancecGMPand all other compliance-related matters where applicable.
- Perform all tasksin accordance withthe standard operating procedures andmaintainstrict compliancetoGMP at all times. Report all the quality issuesimmediatelytoManageror Lead technician.
- If required perform Microbial sampling and swabbing of room and equipment.
- Liaison external vendors for instrument calibration and maintenance.
- If required and depending on product requirement perform chemical and mathematical calculations todetermineproduct potency and endotoxin levels for eachbatchformulation.
- Perform visual inspectionlabelingand packaging on finished drug products.
- Perform in-process sampling on semi-finished drug products. Conduct in-process inspection and checks.
- Any other duties as and when assigned by the Manager.
Requirements
- Minimum O Level NITEC/ITE education/Diploma in relevant field.
- Minimum 3 to 5 years of relevantexperiencesinpharmaceuticalindustry.
- Good understanding of safe working practices and cGMP.
- Highly motivated to work in pharmaceutical Industry.
- Able to work as a team.
- Able to work rotatingshift.
Required Experience:
Senior IC
Key Skills
- Sales Experience
- B2B Sales
- Primary Care Experience
- Biotechnology
- Account Management
- Territory Management
- Computer Literacy
- Outside Sales
- Biomedical
- Botox Experience
- negotiation
- Compounding Medications
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
