Adecco Healthcare & Life Sciences is hiring a contract Micro QC Scientist for our Pharmaceutical partner in Ridgefield, NJ. The anticipated hourly wage for this position is between $44 and $45. Hourly wage may depend upon experience, education, geographic location, and other factors. Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits, Daily Pay, and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria The Micro QC Scientist I is part of the Quality Assurance Department at Ridgefield, NJ. This role is responsible for providing direction, mentoring and completing high level projects for the Micro team. This position also includes product testing, release EM Monitoring, data review and validation. HOURS: Monday - Friday from 8:00 am to 4:30 pm. Some flex in the start and end times may be allowed; weekend work and overtime as required. u2022 Exceptional knowledge of USP, EU and ISO regulations a must. u2022 The candidate must have previous quality control microbiology experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon, endotoxin assays u2022 Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas. u2022 Validation protocol writing, review and execution (or over seeing validation execution) u2022 SOP review, creation and approval u2022 OOS investigations writing/review and approval. u2022 Mentor junior Analysts on testing, trouble shooting and Lab related items u2022 Ensure compliance with all cGMP standards, safety and environmental regulations and company SOPs. u2022 Provide advice to subordinates based on general policies and management guidance. u2022 Ensure that high level projects are completed on schedule and accurately. u2022 Data review of EM sampling, LIMS, logbooks, and other miscellaneous lab data. u2022 Participates in Change Control meetings as the Microbiology Subject Matter Expert and initiates change controls as required. u2022 Support regulatory, third party and internal audits when required u2022 Conveys complex information in a concise manner u2022 Motivate and Develop teams u2022 Interact with Project Teams and cross-functional groups related to site operations Analyst Qualifications: The Micro QC Scientist I is expected to act on and demonstrate the The LEAD competencies: u2022 Act for Change: Embrace change and innovation and initiate new and improved ways of working. u2022 Cooperate transversally: Collaborate effectively with peers, stakeholders and partners across the organization to positively impact business results. u2022 Develop People: Take responsibility for developing ones self and mentor other Micro Personnel in anticipation of future business needs or to assist the micro department. HSE u2022 It is required that individuals care for their own safety and wellbeing. Individuals must promote a safe working environment for employees and contractors working in their area of responsibility. u2022 The individual must support all site HSE policies as well as ensure that work performed is compliant with local HSE regulations. u2022 Individuals must complete all required HSE trainings. Everyone is required to report all accidents and incidents and support investigations in their areas of responsibility. Individuals must ensure timely closure of HSE actions owned by their departments. REQUIREMENTS Education / Experience Physical Requirements include the capacity to lift and carry up to 20 pounds, kneel, reach and stretch, and to stand for at least 4 hours. BA/BS in Microbiology/Biology with 6-10 years experience is required. A thorough understanding of validation testing; write, execute and report validation studies Practical experience in general microbiology laboratory techniques working with bacteria, yeast and mold. Prior experience with, writing protocols, data review, authoring SOPS, Change Controls, out of specification investigations and report writing. Working knowledge of cGMPs in pharmaceuticals/biological/aseptic/medical device manufacturing Excellent technical writing skills Ability to collaborate effectively with personnel and between departments Strong analytical and problem-solving skills Make sound judgement from data Strong communicator Works independently Working knowledge of Word, Excel and PowerPoint Preferred experience with a deviation/CAPA enterprise system Comments Monday-Friday, 40 hours per week, Hours:8:30 to 04:30. Weekend work if needed. Pay Details: $44.00 to $45.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Job Title
QC Scientist I