Quality Control Technician 3 at Merck Sdn Bhd

Jaffrey, New Hampshire, United States -

Full Time

Start Date

Immediate

Expiry Date

30 May, 26

Salary

30.0

Posted On

01 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Bacterial Testing, Filtration Membranes, Troubleshooting, Process Setup, Retention Testing, LIMS, GMP Standards, Equipment Operation, Data Verification, OOS Investigations, Protocol Execution, Validation, EHS, ISO, Computer Skills, Microsoft Office

Industry

Description

Work Location: Jaffrey, New Hampshire Shift: No Department: LS-SC-UJFCF US Jaffrey Wet Lab Hiring Manager: Ashley Emerald This information is for internals only. Please do not share outside of the organization. Your Role Advanced Lab Quality Control Technician with expertise in bacterial testing of biopharmaceutical filtration membranes and devices, focused on ensuring safety, quality, and productivity. Experienced in supporting advanced testing operations through troubleshooting, process setup, and retention testing procedures. Proficient in using Laboratory Information Management Systems (LIMS) to accurately track and document results. Shift hours : 10PM -6AM Duties Include: Test products safely and in accordance with Standard Operating Procedures, Quality and Safety Specifications and GMP standards. Follow procedures to perform required testing independently. Safely set up and operate quality lab test equipment and monitor required inputs and outputs on equipment such as steam systems, pressurized vessels, bacterial challenge systems, and various test stands and support equipment. Support quality lab operations and projects under the supervision of master technicians. Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the work center and the site. Participate in laboratory audits and tours, perform troubleshooting and advanced set-ups, review and verify test and process data with accurate entry into the Laboratory Information Management System (LIMS), support sustainability initiatives, and operate effectively with limited supervision. Accurately complete and review documentation in compliance with GMP standards, initiate and participate in Out of Specification (OOS) investigations, support the execution of protocols, qualifications, and validations, and maintain a clean, organized, and compliant workspace. Physical Attributes Exposure to machinery, chemical reagents, biological materials at Biosafety Levels 1 and 2, and equipment in a laboratory environment. 100% Standing and/or sitting for duration of shift, up to 12 hours. Frequent lifting of 20 - 30 lbs. necessary/Max lifting – 40 to 50 lbs. Bend and twist as needed. Must be able to grasp, manipulate and handle objects consistently and regularly, Fine motor skills are required. Pass a visual acuity test. Who You Are Minimum Qualifications: 3+ years of laboratory experience. High school diploma or GED. Preferred Qualifications: Associate’s degree in Life Science discipline. Bachelor’s degree in any discipline. 3+ years’ experience in an aseptic and cGMP laboratory environment. 1+ years of experience with Laboratory Information Management Systems. Strong knowledge of EHS, ISO, cGMP, and other laboratory and regulatory requirements. Demonstrated computer skills, familiarity with Microsoft Office applications. Reliable and self-motivated. Read, follow and understand Test Methods, Test Specifications, and other technical documentation. Pay Range for this position: $19-$30 per hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Responsibilities

The technician will perform advanced laboratory quality control, focusing on bacterial testing of biopharmaceutical filtration membranes and devices to ensure safety and quality according to GMP standards. Duties include operating specialized test equipment, accurately documenting results in LIMS, and participating in OOS investigations and validations.