MANUFACTURING TECHNICIAN III

1 week ago

Bedford, United States PCI Pharma Services Full time

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. JOB SUMMARY The Manufacturing Technician leads others in a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set inclusive of current GMP/ISO requirements and standards and following all safety Guidelines of PCI. With general supervision, the technician leads and performs all manufacturing operations including but not limited to work functions in equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling and packaging activities for biopharma and medical device products. Addresses non routine matters. Utilizes technical knowledge and experience to resolve complex manufacturing problems. Monitors personnel interaction to ensure proper behaviors. Escalates matters requiring resolution by management. Works with, reviews and revises master production records and standard operating procedures. Trains and guides less experienced personnel. Is a model of the Guardian values and behaviors. JOB DUTIES – Maintains and adheres to safe work habits and all applicable PCI safety procedures and guidelines. Is proactive in identifying safety risks and alerts management to take corrective action. Leads team to successfully and completely accomplish daily tasks Maintains weekly/daily schedule up to date and provides direction to team Accountable for completing daily tasks and reporting and escalating issues to management Works with management to provide a positive culture within operations Mentors less experienced staff in the performance of aseptic techniques Prepares solutions, aseptic filling and labeling of vials under sterile and non-sterile conditions, routine solution and filtration, vial and component preparation and sterilization Assembles, disassembles and operates aseptic filling equipment and lyophilizer equipment in classified cleanroom and controlled non classified environments. Operates vial capper, unloads product from lyophilizers and liquid fill line. Prepares equipment and components for sterilization and Lyophilization Operates processing equipment including autoclaves, ovens, vial washers, and depyrogenation, centrifuges, mills equipment. Assists in the formulation and dispensing of product in a clean room environment per SOPs and MBRs Sanitizes production areas and prepare equipment for production Completes, maintains and reviews documentation related to assigned work, including logbooks, batch records, etc. Trains others on the team, and ensures proper training completion within the team prior to assigning tasks Troubleshoot and resolve problems with equipment or processes in the course of performing job duties Adheres to verbal instructions and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation Identifies, escalates and documents events that deviate from normal operation; perform investigations as needed Maintains compliance, cleanliness and orderliness of operational areas per appropriate SOPs Performs COP, CIP, and SIP operations to prepare equipment for manufacturing operations Demonstrated understanding of sanitization and sterilization practices (build, clean and sterilize equipment to support production operations Inspire and constantly strive to make PCI a great place to work and respected for the quality of its people and products and clients Successfully participates in media fill/aseptic proficiency test PROFESSIONAL SKILLS – Possesses the skill and aptitude to weigh and measure raw materials and operate basic Benchtop instruments Strong ability to plan and prioritize complex activities to meet goals and objectives Strong analytical skills to identify risks and prepare balanced decisions · Excellent organizational, verbal and written communication skills EXPERIENCE – 2 – 4 years in the pharmaceutical or medical device industry finished dose form preferred Strong knowledge of asepic techniques and fill finish experience required Experience in reviewing and creating controlled documents EDUCATION – Requires a high school diploma QUALITIES – Detail oriented with strong mechanical aptitude Positive attitude and strong interpersonal skills to resolve and de-escalate issues. Honesty, integrity, respect and courtesy with leadership and peers Strong commitment to conducting PCI business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of LSNE products and services Resilient, can quickly move forward despite complexities and unexpected events, thrives on challenges to improve skills and abilities Must have ability to work as self-starter and handle multiple priorities in a dynamic cross-functional team based environment PHYSICAL REQUIREMENTS – Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes. Ability to gown and gain entry to controlled manufacturing areas Ability to lift, pull or push equipment requiring up to 25-50 lbs of force Ability to stand for 6 hours in a production suite Ability to work any shift (up to 10 hours) as required dependent on business needs COMMUNICATIONS & CONTACTS – Interacts with cross functional support teams such as Operations, QA, QC, Engineering, R&D, Validation, etc. MANAGERIAL & SUPERVISORY RESPONSIBILITIES - Leads team of manufacturing technicians to complete scheduled activities Assists in leading the manufacturing team in the absence of the supervisor with support from upper management. Raise any personnel related issues to management for resolution Assigns daily tasks TRAVEL –

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