Pilot Plant Operations Specialist, Small Scale Organics (3rd shift)
USA - New Jersey - Rahway, United States
Job Description
The Small Scale Organics Pilot Plant is a (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables gain of critical internal experience with scale-up of manufacturing Good Manufacturing Practices steps, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless technology transfer to commercial sites.
The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs) requirements to meet SSO objectives and customer requirements. The position is responsible for implementing actions to meet S&E and GMP requirements. This position is also responsible for ensuring facility readiness for batch processing and shares accountability for the building performance. Ultimately, this position is expected to work cooperatively with the SSO leadership team and SSO partners to drive overall success and performance of the building, and ultimately strong support for the overall SM PR&D pipeline.
Responsibilities:
Under the scientific direction of a facility lead, the Operations Specialist will participate in equipment setups, raw material sampling and subdivisions, solution preparations, batch processing planning and execution at a pilot scale, process knowledge capture, and troubleshooting equipment with the aim of advancing process development, aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of a variety of reagents, solvents, and active pharmaceutical ingredients during “wet chemistry” operations (performing chemical reactions, extractions, distillations, crystallizations, filtration, drying, etc.) as well as dry powder processing (e.g., dry milling).
Ensure processes are run within the capability constraints of the facility.
Ensure facility readiness with respect to cleaning (including documentation and execution), dummy run and batch execution, building housekeeping, and consumable inventory.
Provide input for incident root cause analysis, reporting, and action items.
Facilitate and drive building improvement projects and corrective/preventative action closures.
Provide input on process setups.
Provide regular feedback to peers to promote a continuous improvement mindset.
Collaborate with all building staff to share and align on best practices.
Actively investigate problem statements and safety observation reports (SORs) to promote fast and efficient closure.
As needed, safely perform High Risk Work involving hazardous energy control.
Identify and follow through on opportunities to improve building flexibility, efficiency, compliance, and safety.
Author lessons learnt and summary reports to capture knowledge gained.
Mentor and help train rotational and new employees.
This position’s primary focus is executing batch production work. Additional responsibilities include coordination, planning, documentation, and other facility improvement activities.
Position Qualifications:
Education Minimum Requirement:
Associate in Science, Associate in Applied Science (ideally in Process Technology), or higher degree in a relevant technical field of study plus at least six (6) years of relevant experience – or –
High School Diploma/GED plus at least eight (8) years of relevant experience in Pharmaceutical, Chemical, Petrochemical or Food Processing/Manufacturing.
Required Experience and Skills:
Strong communication skills to discuss technical problems and a collaborative mindset to interface with cross-functional teams.
A strong mechanical aptitude.
Proficiency in technical writing and the use of word processing, spreadsheet, graphing, and presentation software.
This role requires working on a fixed (steady), 8-hour overnight 3rd shift throughout the year. Onsite presence is required five days a week. Occasional overtime work may be required based on business needs.
Preferred Experience and Skills:
Operations experience in pilot plant or manufacturing environment.
Understanding of/Experience with process scale-up of chemical processes, moving from the laboratory to the pilot scale.
Familiarity with the administration of cGMPs, Good Documentation Practices (GDPs), and S&E regulations as it pertains to pharmaceutical development.
Lean Six Sigma Training / Certification.
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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.
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:
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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.
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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”.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.
Expected US salary range:
$70,500.00 - $110,900.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.
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:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
3rd - NightValid Driving License:
NoHazardous Material(s):
hazardous chemicalsJob Posting End Date:
03/11/2025*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.
ApplyJob Profile
Hybrid Hybrid work Hybrid work model Occasional overtime On-site Onsite Puerto Rico residents only Travel required US and Puerto Rico residents only
Benefits/PerksBonus eligibility Diverse workplace Equal opportunity Equal opportunity employer Flexibility Flexible work Flexible work arrangements Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Paid holidays Retirement benefits Sick Days Training opportunities Vacation
Tasks- Batch processing planning
- Communication
- Compliance
- Documentation
- Equipment setups
- Execution
- Facility readiness
- Innovation
- Leadership
- Planning
- Presentation
- Process development
- Raw material sampling
- Reporting
- Technical writing
- Technology Transfer
- Troubleshooting
Accountability Analysis API Batch processing Best Practices Chemical Chemical reactions Chemistry Cleaning Clinical Collaborative mindset Commercial Communication Compliance Continuous Improvement Coordination Cross-functional Teams Current good manufacturing practices Development Documentation Documentation Practices Drug product Drug product development Education Equipment Execution Filtration Flexibility GMP Good Documentation Practices Good Manufacturing Practices Inclusion Innovation IT Laboratory Leadership Lean Lean Six Sigma Manufacturing Manufacturing Practices Manufacturing Process Manufacturing process development Manufacturing technology Mechanical Mechanical aptitude Mentoring Operations Organization Pharmaceutical Pharmaceutical Development Planning Presentation Process Development Process research Process scale-up Product Development Reporting Research Research and development Root Cause Analysis Safety Safety Compliance Scale-Up Science Six Sigma Teams Technical Technical Writing Technology Technology development Technology Transfer Training Troubleshooting Wet chemistry Word Word Processing Writing
Experience6 years
EducationAS Associate Associate in Applied Science Associate in Science Business Certification Chemistry Degree Development Diploma GED Health Care Higher Higher Degree High School High school diploma IT Relevant experience Science Technology
Certifications TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9