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Jewelry Administrator Jobs (NOW HIRING)

Days Jewelers

Office Manager

Augusta, ME · On-site

Murdock Co Inc., DBA Day's Jewelers is committed to equal employment opportunity and employs all qualified persons without regard to race, color, religion, national origin, sex, age, sexual ...

Day's Jewelers

Office Manager

Augusta, ME · On-site

Murdock Co Inc., DBA Day's Jewelers is committed to equal employment opportunity and employs all qualified persons without regard to race, color, religion, national origin, sex, age, sexual ...

Day's Jewelers

Office Manager

Augusta, ME · On-site

Office Manager $55,000- $72,000 + Incentive Eligible DAY'S JEWELERS The Office Manager's primary ... Administer Bad Check Collection Procedures. * Retain and destroy documents and records per the ...

The Joblink

Office Admin/Assistant

$18.50 - $24.75/hr

About the job Office Admin/Assistant Summary The job brand is based in New York with worldwide ... Following this, the brand has continued to open piercing and jewelry destinations in Rome ...

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Infographic showing various Jewelry Administrator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 10% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Senior Automation Systems Administrator, Manufacturing & Lab Support

Menands, NY • On-site

Regeneron Pharmaceuticals, Inc (USA)
Biotechnology Research and Development • 5 - 10K employees
Learn more about Regeneron Pharmaceuticals, Inc (USA)external

$81K - $110K/yr

Other

Posted 13 days ago

Regeneron rating

8.6

Company rating: 8.6 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

Job description

Role Overview

We are seeking a Senior Automation Systems Administrator to join our IOPS team, providing expertise in the configuration and administration of automated and computerized system software and firmware across our manufacturing and laboratory operations.

Location and Work Model

Menands, New York, United States – Monday to Friday, 8:00 AM to 4:30 PM.

Key Responsibilities
  • Configure and maintain cGMP software for process control, monitoring, and testing.
  • Manage user access, system security, configuration management, and recipe and method management to meet regulatory requirements.
  • Determine data backup and archive requirements and configurations to meet defined RTO and RPOtargets; design and maintain recovery processes.
  • Ensure systems remain in a compliant state by processing change control requests including requirement and design specifications, test plans, technical evaluations, and quality risk assessments.
  • Support and lead system SAT/FAT, validation, and qualification efforts; generate and execute testing and qualification protocols for automated process, monitoring, and testing equipment.
  • Initiate, author, and review Change Controls, EOEs, NOEs, DNFs, risk assessments, impact statements, and corrective and preventive action plans; lead investigations and root cause analyses for non‑compliance issues.
  • Lead multiple small to medium‑size projects related to corrective action, software performance improvement, and new equipment and software implementation.
  • Provide advanced technical automation support and troubleshooting to Manufacturing, Quality Control, and Facilities in accordance with established SOPs and departmental practices.
  • Support system integration with existing platforms such as LIMS and Historian; draft, approve, and follow relevant system software SOPs and policies; identify opportunities for continuous improvement in processes, procedures, and architecture standards.
Qualifications
  • BS/BA in Science, Engineering, or a related field with 5+ years of relevant experience (or equivalent combination of education and experience).
  • Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility preferred.
  • Advanced experience configuring and troubleshooting process control, monitoring, and product release testing systems including design and installation.
  • Expertise in developing Software Lifecycle Documentation, software design documents, technical evaluations, and test plans for cGMP process equipment following GAMP5 guidelines.
  • Current knowledge of cGMP biotech and pharma operations, regulatory and quality policies, procedures, and documentation methods.
Physical and Mandatory Requirements
  • Full cleanroom attire (gown, facemask, hairnet, safety glasses, safety shoes, latex gloves, sanitized with IPA).
  • Ability to remove jewelry, makeup and nail adornments while wearing cleanroom attire.
  • Ability to perform physical requirements for the entirety of a shift (up to 10 hours) in a cleanroom environment, including bending, climbing, crawling, kneeling, reaching (overhead), sitting, squatting, walking, standing, driving, hand manipulation and lifting/pushing/pulling up to 50lbs.
Equal Opportunity Employer Statement

Regeneron is an equal‑opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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