Qc Salary at Amphenol Pcd Inc BETA

Adecco Staffing is assisting a Medical Device Manufacturing facility in Chelmsford MA with their needs for Quality Control Inspectors on 1st and 2nd shift! This is a temp-to-hire opportunity. **Hours -** **1st shift** 5:00am-1:30pm **2nd Shift** 1:00pm-9:30pm **Pay -** **1st shift** $22hr **2nd Shift** $ 24.20hr **JOB SUMMARY:** With limited supervision performs quality inspections for IAB-C. Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in Principal Responsibilities. **RESPONSIBILITIES/DUTIES:** + Compliance to all work instructions, Quality regulations, SOPs, WIs, GMPs and GDPs in the effort to manufacture high quality medical devices at all times. + Training: As required, will train employees to inspection requirements and techniques in manufacturing or other areas. + Retrieval of documentation or work instructions through Agile as necessary, to perform inspections. + Reviews orders and job packets, recording batch numbers and quantiti

Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 Months Pay Range: $28.00 to $33.00 Job Description: The Quality Control Technical Transfer Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing, and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Responsibilities: Applies job skills and company's policies and procedures to complete a variety of tasks. Running test samples for In-Process, Lot Release, and Stability studies. Running test samples f

About the Company: Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health. About the Role: We are seeking a highly motivated and team-oriented professional with entrepreneurial spirit to join our company! This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today’s cutting-edge research into tomorrow’s breakthrough therapies. Responsibilities: Execute analytical test methods in accordance with cGMP regulations i

Summary of position: Responsible for monitoring quality control/assurance requirements of all preservation performed onboard commercial and US Navy vessel in accordance with established Navy regulations and industry standards or specific contractual requirements as defined in the Scope of Work. Collaborate with customer QA personnel on necessary aspects of the job. Essential Job Requirements: Produce/create electronic/handwritten Quality Assurance documentation as Objective Quality Evidence for work performed throughout the preservation process. Develop and Maintain Test and Inspection Plan (TIP) for all assigned jobs. Monitor and document all required readings with regard to, but not limited to, metal anchor tooth (profile), paint wet/dry film thickness (DFT), steel temperatures and all required environmental readings using appropriate equipment to include: micrometer, dry film thickness gauge, infrared thermometer, psychomotor. Ensure all assigned equipment is maintained in good work

Job description: We are seeking a QC Technical Writer to support analytical method validation and transfer projects through technical documentation. This role involves authoring and reviewing method validation protocols, reports, and QC documentation to ensure compliance with ICH, FDA, and EMA regulations. Key Responsibilities: Develop and maintain analytical method documentation for QC release and stability testing of biologics. Author method validation protocols and reports for technology transfer projects. Ensure accuracy and compliance in method validation documents following regulatory standards. Collaborate with QC and regulatory teams to ensure clear, precise documentation. Qualifications & Skills: Strong technical writing experience in QC and regulatory environments. Maintain electronic records using LIMS, ELN, and Empower software Expert knowledge in data analysis. Knowledge of method validation and test methods for QC and external partners. Proficiency in data analysis, compl

About the Company: Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health. About the Role: We are seeking a highly motivated, team-oriented QC Analyst II to join our Microbiology team, reporting to the QC Manager of Microbiology, Saturday through Wednesday shift. This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today’s cutting-edge research into tomorrow’s breakthrough therapies. Responsibilities: Independen

About the Company: Landmark Bio translates groundbreaking research into life-changing medicines. We provide development, manufacturing, and regulatory capabilities to help early-stage life science innovators rapidly progress advanced therapies from bench to clinic. Launched in 2021, and based in Watertown, Mass. Landmark Bio is an unprecedented venture bringing together the best of industry, academia and research hospitals to accelerate life sciences innovation. A public benefit company, our work advances emerging technologies, demonstrates therapeutic potential, and improves human health. About the Role: We are seeking a highly motivated and team-oriented professional with entrepreneurial spirit to join our company! This is an exciting opportunity for a well-qualified candidate to join a rapidly growing company focused on turning today’s cutting-edge research into tomorrow’s breakthrough therapies. We are seeking a QC Analyst II to join the second shift (2pm – 10pm) integrated Analyti

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Responsible for supporting QC testing for