Merck
Associate Specialist, Planning & Scheduling - Clinical Supply Operations - Onsite
- Location
- Rahway, NJ (NJ)
- Posted
- Posted today (employer shows the date only)
- Source
- Workday (employer's applicant tracking system)
- Category
- Operations/Patient Services
- Industry
- Pharma/Biotech
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Job Description
Associate Specialist, Packaging
Summary:
Global Clinical Supply Operations (CSO) is seeking a motivated and detail-oriented Associate Specialist to support clinical supply packaging operations. In this role, you will partner closely with supervisors and cross-functional stakeholders to ensure clinical operation activities are executed in a compliant, efficient, and inspection-ready manner. A strong commitment to regulatory compliance, quality, and adherence to global and site-specific procedures is essential.
Core Responsibilities:
- Partner with Supervisors and Senior Packaging Technicians to prepare rooms and batches for packaging operations, including the development of required packaging documentation.
- Ensure accurate execution and documentation of SAP transactions and perform pre-execution and post-execution reviews of batch records.
- Support and maintain inspection readiness through routine walkthroughs of areas and processes to identify opportunities for improvement and ensure compliance with regulatory expectations.
- Author and/or contribute to incidents of atypical events and clinical complaints, as needed.
- Participate in continuous improvement initiatives to enhance operational efficiency and compliance.
- Support corrective and preventive actions resulting from walkthrough observations and investigations, as needed.
- Monitor area performance against key performance indicators (KPIs), assess trends, and support root cause analysis for missed targets.
- Collaborate effectively with internal partner groups, including Quality, Label Room, Distribution Center, Operations Planning, and Master Planning.
- Complete all documentation in accordance with Good Documentation Practices (GDP).
- Maintain current training and compliance with site safety and quality requirements.
- Perform administrative tasks as needed, including archiving, data entry, recordkeeping, and preparation of metrics reports.
Minimum/Preferred Education:
- Bachelor’s degree.
- A degree in operations management, engineering, supply chain, or related technical field is preferred.
Experience & Skills:
- One or more years’ experience in Technical Operations, related Business Operations or GMP regulated environment, with specific experience in clinical packaging preferred.
- Effective interpersonal and communication skills.
- Demonstrated problem-solving skills.
- Proficient in Microsoft Office (Word, Excel, etc.).
- Detail-oriented and organization skills.
- Ability to quickly learn and complete tasks independently with minimal guidance after training.
- Knowledge of cGMPs, data management, collection and analysis.
- SAP (or equivalent) experience strongly preferred.
Required Skills:
Batch Production Records, Clinical Supplies Management, Compliance Packaging, Continuous Improvement Techniques, Detail-Oriented, Driving Continuous Improvement, Good Manufacturing Practices (GMP), Operational Efficiency, Pharmaceutical Packaging, SAP Products
Preferred Skills:
Clinical Manufacturing, Inspection Readiness, Supply Chain Processes
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
The primary location for this posting is:
USA - New Jersey - Rahway
Where required by law, the compensation range for this role is provided below.
The salary range for the primary location of this role is:
$65,100.00 - $102,500.00
This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. …
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