Specialist, VMF Product Release Position Available In Durham, North Carolina

Job Description Primary Responsibilities:

Support the company site and Quality organization by performing tasks associated with the site’s goals and initiatives as they relate to batch release and Quality requirements and standards. This involves the items as listed below, but is not limited to the following: Product release of batches for the Vaccine Manufacturing Facility (VMF) Completion of tasks required to release batches such as

DOM/SLED

Review, TOR/TOCS Review, BSA/rHA/Cell Dose Review, Thermal-Stability review, associated lot Review, Protocol Generation, Batch CBER Submission, tasks associated with batch sample shipment, etc. Serve as SME (Subject Matter Expert) to support internal and regulatory audits Support and lead department related initiatives associated with KPIs (Key Performance Indicators), process improvements, and other goal-driven directives— own project management opportunities, by leading and participating in process improvement, learning events, and/or business support initiatives, as guided or approved by Quality management Provide Quality input, direction, and approval of Quality Notifications (QNs) Assist with providing product related information to support Change Requests (CRs). Author, review, and approve SOPs. Train employees on new or revised processes or procedures. Consults on an as-needed basis with next-level manager from a release perspective on more complex decisions and/or issues that impact other units with inter-related processes. Other duties as requested by Management.

Minimum Education Requirement and Experience:

Bachelor’s degree (BA/BS) in Biology, Biochemistry, Chemistry, Engineering or other relevant discipline with a minimum of five (5) years of experience supporting the Biotech/pharmaceutical manufacturing industry, specifically in operations, technical operations, validation and/or process Quality Assurance.

Required Experience and Skills:

QA Release experience in electronic systems of at least 3 years. Has in-depth knowledge of cGMPs and domestic and international regulatory requirements. Is expected to possess a high degree of problem-solving ability. Must have demonstrated ability to independently manage multiple high level/ priority projects, ensuring timely completion.

Preferred Experience and Skills:

Experience with electronic Batch Records (MES/PAS-X) cGMP experience in a sterile, bulk or finished pharmaceutical/biotech environment. Experience with release or disposition of Product, Raw Materials, and Components Release Experience with

SAP, MRP/ERP

systems and/or GLIMS Flexibility to support on-call off shift and hyper-care related activities. VETJOBS #EBRG 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. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights

EEOC GINA

Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills 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 U.S. Hybrid Work Model Effective 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 Ordinance Los 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 Ordinance 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:

Regular Relocation:

No relocation

VISA Sponsorship:

No Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid Shift:

1st –

Day Valid Driving License:

No Hazardous Material(s):

N/A Job Posting End Date:

04/26/2025 •A 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. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.