Associate Specialist, Quality

Job DescriptionOur Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.Position Responsibilities:Conducts testing and associated tasks without errors per applicable SOPs and protocolsComplies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written.Works in a team environment to accomplish departmental goalsDevelops expertise in assigned assays/techniquesAssists in the maintenance of the lab including routine housekeeping activities and waste managementMaintenance of lab equipmentMay be required to perform off shift work as required to support operations and perform other duties as assignedEducation Minimum Requirement:B.S. degree in science field, preferably biology, biochemistry, biotechnology or Biomedical Sciences.Required Experience and Skills:A minimum of 1 year experience working in a laboratory setting.Must be able to discriminate colors for characteristics tests or related assays.Demonstrated interpersonal, technical aptitude, and problem-solving skills.Experience in using pipettes (single channel, Multichannel)Experience with the pH meter instrument and analytical balances.Ability to perform basic scientific math, must have strong computer skills and proficiency with MS Office applications required.Must be flexible and able to manage multiple assigned tasks.Must have attention to details and good documentation skill.Communicates well with co-workers and superiorsAbility to analyze data and write up resultsAble to lift 25 lbs.Preferred Experience and Skills:Prior experience in a GMP Quality Control laboratory strongly preferredCell culture maintenance and aseptic techniques experienceFamiliar with cell-based assaysLearn new methods and expand capabilities within the laboratoryKnowledge of safety guidelines in a laboratory environmentBe sharp, self-motivated, and able to thrive in a fast-paced dynamic environment.NOTICE FOR INTERNAL APPLICANTSIn accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders.Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics.U.S. Hybrid Work ModelEffective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, generally Tuesday, Wednesday and either Monday or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.Search Firm Representatives Please Read CarefullyMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.Employee Status:

RegularRelocation:

No relocationVISA Sponsorship:

NoTravel Requirements:

No Travel RequiredFlexible Work Arrangements:

Not ApplicableShift:

1st - DayValid Driving License:

NoHazardous Material(s):

YesJob Posting End Date:

10/3/2024

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