Job Details

ID #52644410
Estado Pennsylvania
Ciudad Westpoint
Fuente Merck
Showed 2024-10-05
Fecha 2024-10-05
Fecha tope 2024-12-03
Categoría Etcétera
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Specialist, Quality Control

Pennsylvania, Westpoint
Aplica ya

Job DescriptionPosition Overview – Basic Functions & ResponsibilityThe Global Quality - Large Molecule Analytical Sciences (GQ-LMAS) team leads the global analytical technical oversight of late-stage pipeline programs through commercialization and launch as well as product lifecycle management support for Large Molecules (Vaccine and Biologics) and Cross-Modality Compounds (Antibody Drug Conjugates).The Sample Management Team sits under Biologics Critical Reagents and coordinates sample shipments, chain of custody, and aliquots/fill activities to support the late-stage pipeline programs and launch milestones.Primary Activities, but not limited to :

Serve as logistics coordinator for GQ-LMAS

Perform Deviation management and execute change controls.

Proficient in Electronic Notebook, EDMS, LIMS systems, BioInventory

Perform Second Person Review

Self-motivated with a positive attitude and proven performance record

Ensuring work is compliant with GXP/cGMP regulatory expectations.

Perform Inventory management.

Revise and Review SOPs

Train new employees

Minimum Education Required and Experience:

Bachelor’s Degree (BA/BS) with a concentration in biology, chemistry, biochemistry or related sciences and a minimum of one (1-2) year of relevant sample management experience.

Required Skills and Experience:

Has the ability to lift 40lbs

Has a valid Driver’s License and can operate vehicles

Has at least 1-2 years working experience in a GXP laboratory environment with knowledge of aseptic technique

Has 1-2 years Sample Management experience

Has ability to work independently and within a cross-functional team

Has ability to learn new techniques and multitask efficiently

Has good technical, communication (oral and written), interpersonal, and teamwork skills

Preferred Experience and Skills

Ability to manage assignments, working towards deadlines within a schedule.

High level of attention to detail, in particular with the preparation of GMP deviation records.

Technical writing experience

Experience with Quality Audits including speaking with auditors, preparing responses, and opening CAPAs.

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.Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)US 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 (https://survey.sogosurvey.com/r/aCdfqL) 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. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088EEOCKnowYourRights1020.pdf)EEOC GINA Supplement​Pay Transparency Nondiscrimination (https://www.dol.gov/sites/dolgov/files/OFCCP/pdf/pay-transp%20EnglishformattedESQA508c.pdf)We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)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, Monday - 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.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring OrdinanceSearch 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. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status:RegularRelocation:No relocationVISA Sponsorship:NoTravel Requirements:10%Flexible Work Arrangements:HybridShift:1st - DayValid Driving License:YesHazardous Material(s):OEB4Job Posting End Date:10/12/2024A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.Job Posting End Date: 10/12/2024A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.Requisition ID: R313621

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