Job Description
Working closely with Senior Packaging Technicians, work within a team environment to execute clinical packaging and labeling activities, including material, room and equipment staging, execution and documentation of operations, and room clearance and cleaning. Perform visual inspection of rooms and equipment post-cleaning. Provide hands-on training for new employees. Support additional operational activities in support of sampling and material transfer. Performs all tasks related to clinical label printing production. Maintain training and compliance with site safety and quality requirements.
This role is part of a shift, with specific requirements for start and stop times and requires onsite presence five days a week.
General Responsibilities: - Maintain cGMP and safety training to site requirements.
- Follow cGMP, Standard Operating Procedure (SOP) and safety requirements in all activities.
- Report potential quality events, non-conformance to GMPs/SOPs when observed.
- Ensure all paperwork is properly executed using Good Documentation Practices
- Occasional overtime and weekend work may be requested.
- Interact with employees within own department as well as frequent interactions with employees from other groups/departments.
- Support investigations and internal inspections.
- Supports creative problem solving, provides detailed analysis of issues and anticipates technical problems and obstacles.
- Undertake specific projects within the group on as needed basis.
Warehouse-specific Responsibilities: - Perform incoming material receipt, clinical site drug returns and sample management.
- Receive, inspect and store all warehouse inventory.
- Execute sample collection activities.
- Perform inventory functions such as weekly replenishment, posting of Excess & Obsolete inventory and min/max changes.
- Coordinate and execute discard process for, but not limited to, expired and non-available inventory.
- Process order management and material staging in support of packaging/labeling work centers.
- Emergency cold vault coverage, when needed.
- Perform regular cycle counts, ensuring system inventory accuracy.
- Manages shipping activities, freight and logistics functions (pick, pack, label, schedule, ship)
- May be assigned to coordinate and/or prioritize warehouse activities.
- Manages distribution of bulk and finished good clinical materials.
Documentation: - Creation of Packaging documents according to SOPs.
- Ensures correct documentation of transactions within SAP.
- Documentation according to Good Documentation Practice (GDP) Guideline.
- Check of correct content of written Good Manufacturing Practice (GMP) documents.
Education: - High School Diploma or equivalent required
Experience & Skills: - Growth mindset
- Team player
- Desire to learn packaging operations.
- Excellent interpersonal and communication skills.
- Detail-oriented and organized
Requirements: - Ability to repetitively lift, carry, push and pull up to 50 lbs. required for Packaging and Warehouse roles.
- Ability to quickly learn new systems required.
- Demonstrate competency and in-depth knowledge of all processes, methods and procedures related to GMP environment and area-specific tasks.
- Experience with Microsoft applications (Word, Outlook)
- SAP experience is highly desired
- Cold Chain experience is highly desired
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Required Skills: Accountability, Analytical Problem Solving, Biological Manufacturing, Cleanroom Gowning, Computer Literacy, GMP Operations, Good Manufacturing Practices (GMP), Laboratory Processes, Machinery Operation, Manufacturing Quality Control, Mechanical Equipment Maintenance, Operations Management, Packaging Operations, Pharmaceutical Manufacturing, Production Scheduling, Shift Work, Standard Operating Procedure (SOP) Writing, Vaccine Production
Preferred Skills: 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:
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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.
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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: No Travel Required
Flexible Work Arrangements: Not Applicable
Shift: 1st - Day
Valid Driving License: No
Hazardous Material(s): n/a
Job Posting End Date: 01/22/2026
*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. Requisition ID: R381171
Job Tags
Full time, For contractors, Casual work, Work at office, Local area, Remote work, Relocation, Visa sponsorship, Flexible hours, Shift work, 3 days per week,