What are the responsibilities and job description for the Associate Specialist - Reagent Inventory Management position at Merck?
Job Description
Our company's Regulated Bioanalytics (BA) group in West Point, PA supports regulated bioanalytical assay development and validation, and testing for the development of small molecule, vaccines and biotherapeutics. We are seeking a highly talented and motivated individual to work within the Lab Systems and Sample Management team to support the management, tracking, acquisition/preparation, and shipping of critical reagents that support a variety of bioanalytical methods at our company. This individual will also help to define, maintain, and enhance the processes and reagent tracking software used by the team.
Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.
Responsibilities:
Manage the Regulated Bioanalytical critical reagent inventory, including receipt, storage, and retrieval of reagents
Perform reagent aliquoting through manual pipetting or automated liquid handler lab capabilities
Generate & apply reagent barcodes and track reagent information (e.g. location, expiry, Certificate of Analysis, etc.) within a reagent inventory management system
Partner with IT and bioanalytical teams for the evaluation and implementation of new reagent barcoding and tracking systems
Develop a collaborative relationship with off-site storage partners for the management of reagent and samples stored off-site.
Support the management of freezers dedicated to critical reagents; serve as point of contact for temperature alarm handling
Coordinate domestic and international shipping of critical reagents to internal & external partners
Prepare and/or qualify general reagents for use within bioanalytical assays
Partner with the sample management team to support receipt and distribution of GLP and clinical study samples
Develop into a subject matter expert in terms of reagent tracking, software and related processes
Author SOPs or job aids associated with the lifecycle of critical reagents
Position Qualifications:
Education Minimum Requirement:
Associates degree in Biology, Chemistry, Medical Technology or related sciences with at least 3 years of experience or a BA/BS with 1 year of laboratory experience
Required Experience and Skills:
Experience working within a laboratory, preferably working with clinical or pre-clinical samples
Experience utilizing an inventory management system, such as a laboratory information management system (LIMS) or related databases
Capable of working independently with day-to-day tasks under moderate supervision
Possesses good verbal and written communication skills and comfortable interacting with a variety of on-site and off-site collaborators.
Proficiency with Microsoft Office applications, including Excel, with an intermediate ability to generate spreadsheets of various complexities
Computer savvy & capable of evaluating and developing expertise with new applications
Ability to work efficiently and to adapt to changes in assignments consistent with new or changing project priorities
Ability to track and prioritize incoming requests and execute in a fast-paced environment
#MSJR
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.
Who we are …
We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What we look for …
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.
NOTICE FOR INTERNAL APPLICANTS
In 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.
New hires in office-based roles in the US & Puerto Rico will be required, subject to applicable law, to demonstrate that they have been fully vaccinated for COVID-19 or qualify for a medical or religious exemption to this vaccination requirement that can be accommodated without an undue burden to the operation. However, subject to applicable law, employees working in roles that the Company determines require routine collaboration with external stakeholders, such as employees in health services, customer facing commercial, or research based roles, will be required to be fully vaccinated as a condition of employment.
Current Employees apply HERE
Current Contingent Workers apply HERE
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 if you need an accommodation during the application or hiring process.
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster
EEOC GINA Supplement
OFCCP EEO Supplement
Pay Transparency Nondiscrimination
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. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Search Firm Representatives Please Read Carefully
Merck & 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:
DomesticVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Work WeekShift:
1st - DayValid Driving License:
YesHazardous Material(s):
Number of Openings:
1Requisition ID:R185327