Manufacturing Tech Lead

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.The Manufacturing Technician III/IV 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.Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.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 tasksMaintains weekly/daily schedule up to date and provides direction to teamAccountable for completing daily tasks and reporting and escalating issues to managementWorks with management to provide a positive culture within operationsMentors less experienced staff in the performance of aseptic techniquesPrepares solutions, aseptic filling and labeling of vials under sterile and non-sterile conditions, routine solution and filtration, vial and component preparation and sterilizationAssembles, 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 LyophilizationOperates 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 MBRsSanitizes production areas and prepare equipment for productionCompletes, 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 tasksTroubleshoot and resolve problems with equipment or processes in the course of performing job dutiesAdheres to verbal instructions and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentationIdentifies, escalates and documents events that deviate from normal operation; perform investigations as neededMaintains compliance, cleanliness and orderliness of operational areas per appropriate SOPsPerforms COP, CIP, and SIP operations to prepare equipment for manufacturing operationsDemonstrated understanding of sanitization and sterilization practices (build, clean and sterilize equipment to support production operationsInspire and constantly strive to make PCI a great place to work and respected for the quality of its people and products and clientsSuccessfully participates in media fill/aseptic proficiency testSpecial Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes.Ability to gown and gain entry to controlled manufacturing areasAbility to lift, pull or push equipment requiring up to 25-50 lbs of forceAbility to stand for 6 hours in a production suiteAbility to work any shift (up to 10 hours) as required dependent on business needsWork Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Interacts with cross functional support teams such as Operations, QA, QC, Engineering, R&D, Validation, etc.Leads team of manufacturing technicians to complete scheduled activitiesRaise any personnel related issues to management for resolutionAssigns daily tasksTRAVEL – <10% Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.2 – 4 years in the pharmaceutical or medical device industry finished dose form preferredStrong knowledge of aseptic techniques and fill finish experience requiredExperience in reviewing and creating controlled documentsRequires a high school diploma Possesses the skill and aptitude to weigh and measure raw materials and operate basic Benchtop instrumentsStrong ability to plan and prioritize complex activities to meet goals and objectivesStrong analytical skills to identify risks and prepare balanced decisionExcellent organizational, verbal and written communication skillsDetail oriented with strong mechanical aptitudePositive attitude and strong interpersonal skills to resolve and de-escalate issues.Honesty, integrity, respect and courtesy with leadership and peersStrong commitment to conducting PCI business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI products and servicesResilient, can quickly move forward despite complexities and unexpected events, thrives on challenges to improve skills and abilitiesMust have ability to work as self-starter and handle multiple priorities in a dynamic cross-functional team based environment#LI-LL1Join us and be part of building the bridge between life changing therapies and patients. Let’s talk futureEqual Employment Opportunity (EEO) Statement:PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.SummaryLocation: Bedford, NH, USAType: Full time