Lead Production Floor Supervisor - ISO/GMP
NextPhase Medical Devices LLC
Arterex Medical in Mansfield, MA seeks a Production Floor Supervisor to lead multiple lines, train staff, and ensure on-time, quality builds. You will drive manufacturing excellence on the floor, work with cross-functional teams, and mentor operators in a fast-paced environment. The role emphasizes hands-on leadership, adherence to ISO 13485:2016 and 21 CFR 820, and a commitment to safety, documentation, and continuous improvement on the shop floor. #J-18808-Ljbffr NextPhase Medical Devices LLC
- ...Join Arterex Medical as a Production Supervisor, where you’ll drive high-quality... ...excellence on the manufacturing floor. Job Summary: The role of... ..., experience in an ISO 13485:2016, FDA Quality System... ...Documentation Practices) and GMP (Good Manufacturing Practices...SuggestedTemporary workRemote work
- ...visual inspection. You will ensure material readiness and contemporaneous MES/eBR documentation, enabling compliant production. The role requires 2-4 years of GMP manufacturing experience or entry-level with training, and is a 12-hour night shift on-site. #J-18808-Ljbffr...SuggestedNight shift
- Scorpion Therapeutics in Massachusetts is seeking a Senior Manufacturing Associate I to execute GMP manufacturing processes for mRNA and LNP drug substances, supporting both clinical and commercial vaccines. The role focuses on aseptic processing, formulation, filling,...Suggested
- ...a Manufacturing Team Lead to work 1st shift (7:0... ...directions to assigned production associates, which includes... ...to the Production Supervisor and will work in our Mansfield... ...and experience with GMP, ISO, FDA, and quality... ...the production floor for daily production....SuggestedHourly payLocal areaMonday to FridayDay shift
$100k
About the job Night production supervisor This position supports a leading innovator in sustainable food packaging by overseeing overnight (7p7a) thermoforming... ...quality and compliance with regulatory standards (SQF/ISO), taking corrective action if needed Enforce safety...SuggestedHourly payRelocationNight shiftRotating shift- ...Canton, MA, seeks a QA Specialist I, Document Control to own the GMP document control program for the vaccine Drug Substance site. You... ...support inspection readiness and regulatory alignment. You will lead doc control workflows, archiving, deviations, CAPAs, and KPIs to...
$109.25k - $149.5k
...and set new standards of care.SUMMARYThe Lead Auditor, Quality Compliance will form part... ...performed in compliance with recognized ISO, GMP, GDP, GCP, and GLP, global policies/procedures... ..., Supply Chain, Regulatory Affairs, Product Development, and business leaders as required...Full timeTemporary workWork experience placement- ..., identify gaps, and drive improvements with suppliers and customers to resolve issues. Responsibilities include leading ISO 9001 audits, guiding production and inspection staff, and ensuring nonconforming materials are handled cost-effectively. A Bachelor's in business...
- Moderna is seeking a Manufacturing Associate II, DP Operations to perform core cGMP unit operations including formulation, aseptic filling, and in-process controls. The role emphasizes accurate documentation, adherence to SOPs, and collaboration across QA, QC and facilities...Night shiftWeekend work
- ...Production Supervisor About Us: Founded in 1953, Electrical Components International (ECI) is one of the world's leading suppliers of electrical distribution systems, control box assemblies, and other critical engineered components for diversified markets. With...For contractorsLocal area
$95k - $130k
...seeking an experienced, hands-on Quality Lead to lead and own the company's... ...risk management activities across the product lifecycle.Analyze field performance... ...management.Demonstrated expertise in ISO 13485, FDA 21 CFR Part 820, GMP, and regulatory inspection readiness...Work experience placementWork at office$26 - $29 per hour
...assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed... ...spend at least 80 - 90% of the time on the manufacturing floor Working closely with related functional areas to...Hourly payTemporary workMonday to FridayShift workNight shiftDay shiftAfternoon shift- Maersk Warehousing and Distribution USA LLC in Franklin, MA is seeking an Assistant Manager for our Last Mile facility. You will develop vendor relations, coordinate hauler-to-client communications, and oversee on-site delivery operations with daily GPS-driven dispatch ...Monday to Friday
$90k - $110k
...If you are front line Supervisor looking for an opportunity to grow, Emerson has an exciting... ...the day-to-day operations to maximize production while improving our safe workplace, reducing... ...members based on business needs. Lead problem solving activities of any issue...Hourly payContract workTemporary workLocal areaFlexible hours- ...retailers for more than 30 years to drive productivity and profitable growth. For our growing... ...Supervises the Service Bureau associates and Lead(s). Responsible for all Service Bureau... ...Follows any other instructions given by supervisors and/or management to complete other...Contract workWork at office
- Unicom Engineering Inc. seeks a Quality Systems Manager to lead the development, implementation, and continual improvement of the Integrated Management System (IMS). You will drive governance for ISO 9001, ISO 14001, ISO 27001, and other applicable standards, ensuring...
- # Production Supervisor (2nd Shift)## Job Introduction**Who We Are**IQE is a leading global supplier of compound semiconductor wafers and advanced materials. As one of the only... ...internally and within the scope of business, ISO, and regulatory requirements as it pertains...Full timeContract workWork at officeWorldwideAfternoon shift
$35 - $37 per hour
...Description Job Description Manufacturing Associate II, Drug Product Operations Role Overview The Manufacturing Associate II,... ...conducts batch record reviews. The Associate ensures accurate GMP documentation and collaborates cross-functionally to maintain...Hourly payPermanent employmentTemporary workWork experience placementShift workNight shift- ...inventory records and accurate batch records. Inspect finished products for adherence to specifications. Assist with batch record... ..., principles, and processes. Strong understanding of current GMP and safety standards. Ability to function in a dynamic environment...Temporary workWork experience placementLocal areaFlexible hoursRotating shift
$27 - $28 per hour
...Associate Job Description This role supports a leading biotechnology manufacturing facility that produces gene therapy products used to treat rare and genetic diseases. As a... ..., or operations, preferably within a GMP-regulated environment. High school diploma...Weekly payContract workTemporary workWork at officeFlexible hoursShift workRotating shiftWeekday work$53.5k - $85.6k
...substance in a highly controlled, regulated GMP environment. The work is technical,... ...cleanliness, control, and readiness of the production area Use manufacturing systems and equipment... ...in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure...Permanent employment- Role Senior Manufacturing Associate I in mRNA and LNP drug substance operations, responsible for executing GMP manufacturing processes for clinical and commercial vaccines. Core responsibilities aseptic processing, formulation, filling, dispensing, and documentation compliance...Work at office
$63.2k - $100.9k
...a High School Diploma with equivalent experience. 2-4 years in GMP manufacturing or similar environment preferred; we will train strong... ...Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines...Permanent employmentWork from homeNight shiftWeekend work$74k - $118.4k
...and combining mRNA and LMX/LNP for clinical pipeline products as well as commercial seasonal vaccines in a GMP regulated environment. A Sr. Manufacturing... ...our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine...Permanent employmentSeasonal workWork at officeWork from home$74k - $118.4k
...Manufacturing Associate I, Drug Product Label & Packaging is an... ...activities, supports and may lead line readiness and changeovers... ...of corrective actions on the floor. Train, coach, and support qualification... ...3-5 years of experience in GMP manufacturing or regulated...Permanent employmentShift workWeekend work- Job Summary The Production Lead is responsible for overseeing daily packaging and labeling operations in a regulated manufacturing environment... ...role ensures compliance with Good Manufacturing Practices (GMP/cGMP), Good Documentation Practices (GDP), Standard Operating...Work at office
$53.5k - $85.6k
...substance in a highly controlled, regulated GMP environment. The work is technical,... ...cleanliness, control, and readiness of the production area Use manufacturing systems and equipment... ...in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure...Permanent employmentLocal areaWork from home$63.2k - $100.9k
...a High School Diploma with equivalent experience. 2-4 years in GMP manufacturing or similar environment preferred; we will train strong... ...Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines...Permanent employmentWork from homeNight shiftWeekend work$74k - $118.4k
...Manufacturing Associate I, Drug Product Label & Packaging is an... ...activities, supports and may lead line readiness and changeovers... ...of corrective actions on the floor.* Train, coach, and support qualification... ...3-5 years of experience in GMP manufacturing or regulated...Work from homeShift workWeekend work- ...Manufacturing Associate I to independently perform manufacturing unit operations in a GMP environment, including aseptic processing of mRNA and LMX/LNP for clinical and commercial products. The role requires adherence to SOPs, safety protocols, and data integrity, with...
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